Recent from talks
Nothing was collected or created yet.
Impact evaluation
View on WikipediaImpact evaluation assesses the extent to which an intervention (such as a project, program or policy) is causally responsible for observed outcomes, intended and unintended.[1] In contrast to outcome monitoring, which examines whether targets have been achieved, impact evaluation is structured to answer the question: how would outcomes such as participants' well-being have changed if the intervention had not been undertaken? This involves counterfactual analysis, that is, "a comparison between what actually happened and what would have happened in the absence of the intervention."[2] Impact evaluations seek to answer cause-and-effect questions. In other words, they look for the changes in outcome that are directly attributable to a program.[3]
Impact evaluation helps people answer key questions for evidence-based policy making: what works, what doesn't, where, why and for how much? It has received increasing attention in policy making in recent years in the context of both developed and developing countries.[4] It is an important component of the armory of evaluation tools and approaches and integral to global efforts to improve the effectiveness of aid delivery and public spending more generally in improving living standards. Originally more oriented towards evaluation of social sector programs in developing countries, notably conditional cash transfers, impact evaluation is now being increasingly applied in other areas such as agriculture, energy and transport.
Counterfactual evaluation designs
[edit]Counterfactual analysis enables evaluators to attribute cause and effect between interventions and outcomes. The 'counterfactual' measures what would have happened to beneficiaries in the absence of the intervention, and impact is estimated by comparing counterfactual outcomes to those observed under the intervention. The key challenge in impact evaluation is that the counterfactual cannot be directly observed and must be approximated with reference to a comparison group. There are a range of accepted approaches to determining an appropriate comparison group for counterfactual analysis, using either prospective (ex ante) or retrospective (ex post) evaluation design. Prospective evaluations begin during the design phase of the intervention, involving collection of baseline and end-line data from intervention beneficiaries (the 'treatment group') and non-beneficiaries (the 'comparison group'); they may involve selection of individuals or communities into treatment and comparison groups. Retrospective evaluations are usually conducted after the implementation phase and may exploit existing survey data, although the best evaluations will collect data as close to baseline as possible, to ensure comparability of intervention and comparison groups.
There are five key principles relating to internal validity (study design) and external validity (generalizability) which rigorous impact evaluations should address: confounding factors, selection bias, spillover effects, contamination, and impact heterogeneity.[5]
- Confounding occurs where certain factors, typically relating to socioeconomic status, are correlated with exposure to the intervention and, independent of exposure, are causally related to the outcome of interest. Confounding factors are therefore alternate explanations for an observed (possibly spurious) relationship between intervention and outcome.
- Selection bias, a special case of confounding, occurs where intervention participants are non-randomly drawn from the beneficiary population, and the criteria determining selection are correlated with outcomes. Unobserved factors, which are associated with access to or participation in the intervention, and are causally related to the outcome of interest, may lead to a spurious relationship between intervention and outcome if unaccounted for. Self-selection occurs where, for example, more able or organized individuals or communities, who are more likely to have better outcomes of interest, are also more likely to participate in the intervention. Endogenous program selection occurs where individuals or communities are chosen to participate because they are seen to be more likely to benefit from the intervention. Ignoring confounding factors can lead to a problem of omitted variable bias. In the special case of selection bias, the endogeneity of the selection variables can cause simultaneity bias.
- Spillover (referred to as contagion in the case of experimental evaluations) occurs when members of the comparison (control) group are affected by the intervention.
- Contamination occurs when members of treatment and/or comparison groups have access to another intervention which also affects the outcome of interest.
- Impact heterogeneity refers to differences in impact due by beneficiary type and context. High quality impact evaluations will assess the extent to which different groups (e.g., the disadvantaged) benefit from an intervention as well as the potential effect of context on impact. The degree that results are generalizable will determine the applicability of lessons learned for interventions in other contexts.
Impact evaluation designs are identified by the type of methods used to generate the counterfactual and can be broadly classified into three categories – experimental, quasi-experimental and non-experimental designs – that vary in feasibility, cost, involvement during design or after implementation phase of the intervention, and degree of selection bias. White (2006)[6] and Ravallion (2008)[7] discuss alternate Impact Evaluation approaches.
Experimental approaches
[edit]Under experimental evaluations the treatment and comparison groups are selected randomly and isolated both from the intervention, as well as any interventions which may affect the outcome of interest. These evaluation designs are referred to as randomized control trials (RCTs). In experimental evaluations the comparison group is called a control group. When randomization is implemented over a sufficiently large sample with no contagion by the intervention, the only difference between treatment and control groups on average is that the latter does not receive the intervention. Random sample surveys, in which the sample for the evaluation is chosen randomly, should not be confused with experimental evaluation designs, which require the random assignment of the treatment.
The experimental approach is often held up as the 'gold standard' of evaluation. It is the only evaluation design which can conclusively account for selection bias in demonstrating a causal relationship between intervention and outcomes. Randomization and isolation from interventions might not be practicable in the realm of social policy and may be ethically difficult to defend,[8][9] although there may be opportunities to use natural experiments. Bamberger and White (2007)[10] highlight some of the limitations to applying RCTs to development interventions. Methodological critiques have been made by Scriven (2008)[11] on account of the biases introduced since social interventions cannot be fully blinded, and Deaton (2009)[12] has pointed out that in practice analysis of RCTs falls back on the regression-based approaches they seek to avoid and so are subject to the same potential biases. Other problems include the often heterogeneous and changing contexts of interventions, logistical and practical challenges, difficulties with monitoring service delivery, access to the intervention by the comparison group and changes in selection criteria and/or intervention over time. Thus, it is estimated that RCTs are only applicable to 5 percent of development finance.[10]
Randomised control trials (RCTs)
[edit]RCTs are studies used to measure the effectiveness of a new intervention. They are unlikely to prove causality on their own, however randomisation reduces bias while providing a tool for examining cause-effect relationships.[13] RCTs rely on random assignment, meaning that that evaluation almost always has to be designed ex ante, as it is rare that the natural assignment of a project would be on a random basis.[14] When designing an RCT, there are five key questions that need to be asked: What treatment is being tested, how many treatment arms will there be, what will be the unit of assignment, how large of a sample is needed, how will the test be randomised.[14] A well conducted RCT will yield a credible estimate regarding the average treatment effect within one specific population or unit of assignment.[15] A drawback of RCTs is 'the transportation problem', outlining that what works within one population does not necessarily work within another population, meaning that the average treatment effect is not applicable across differing units of assignment.[15]
Natural experiments
[edit]Natural experiments are used because these methods relax the inherent tension uncontrolled field and controlled laboratory data collection approaches.[16] Natural experiments leverage events outside the researchers' and subjects' control to address several threats to internal validity, minimising the chance of confounding elements, while sacrificing a few of the features of field data, such as more natural ranges of treatment effects and the presence of organically formed context.[16] A main problem with natural experiments is the issue of replicability. Laboratory work, when properly described and repeated, should be able to produce similar results. Due to the uniqueness of natural experiments, replication is often limited to analysis of alternate data from a similar event.[16]
Non-experimental approaches
[edit]Quasi-experimental design
[edit]Quasi-experimental approaches can remove bias arising from selection on observables and, where panel data are available, time invariant unobservables. Quasi-experimental methods include matching, differencing, instrumental variables and the pipeline approach; they are usually carried out by multivariate regression analysis.
If selection characteristics are known and observed, they can be controlled for to remove the bias. Matching involves comparing program participants with non-participants based on observed selection characteristics. Propensity score matching (PSM) uses a statistical model to calculate the probability of participating on the basis of a set of observable characteristics and matches participants and non-participants with similar probability scores. Regression discontinuity design exploits a decision rule as to who does and does not get the intervention to compare outcomes for those just either side of this cut-off.
Difference in differences or double differences, which use data collected at baseline and end-line for intervention and comparison groups, can be used to account for selection bias under the assumption that unobservable factors determining selection are fixed over time (time invariant). Difference in differences can also be applied to multiple time points and when an intervention is incrementally introduced in phases.[17]
Instrumental variables estimation accounts for selection bias by modelling participation using factors ('instruments') that are correlated with selection but not the outcome, thus isolating the aspects of program participation which can be treated as exogenous.
The pipeline approach (stepped-wedge design) uses beneficiaries already chosen to participate in a project at a later stage as the comparison group. The assumption is that as they have been selected to receive the intervention in the future they are similar to the treatment group, and therefore comparable in terms of outcome variables of interest. However, in practice, it cannot be guaranteed that treatment and comparison groups are comparable and some method of matching will need to be applied to verify comparability.
Non-experimental design
[edit]Non-experimental impact evaluations are so-called because they do not involve a comparison group that does not have access to the intervention. The method used in non-experimental evaluation is to compare intervention groups before and after implementation of the intervention. Intervention interrupted time-series (ITS) evaluations require multiple data points on treated individuals before and after the intervention, while before versus after (or pre-test post-test) designs simply require a single data point before and after. Post-test analyses include data after the intervention from the intervention group only. Non-experimental designs are the weakest evaluation design, because to show a causal relationship between intervention and outcomes convincingly, the evaluation must demonstrate that any likely alternate explanations for the outcomes are irrelevant. However, there remain applications to which this design is relevant, for example, in calculating time-savings from an intervention which improves access to amenities. In addition, there may be cases where non-experimental designs are the only feasible impact evaluation design, such as universally implemented programmes or national policy reforms in which no isolated comparison groups are likely to exist.
Biases in estimating programme effects
[edit]Randomized field experiments are the strongest research designs for assessing program impact. This particular research design is said to generally be the design of choice when it is feasible as it allows for a fair and accurate estimate of the program's actual effects (Rossi, Lipsey & Freeman, 2004).
With that said, randomized field experiments are not always feasible to carry out and in these situations there are alternative research designs that are at the disposal of an evaluator. The main problem though is that regardless of which design an evaluator chooses, they are prone to a common problem: Regardless of how well thought through or well implemented the design is, each design is subject to yielding biased estimates of the program effects. These biases play the role of exaggerating or diminishing program effects. Not only that, but the direction the bias may take cannot usually be known in advance (Rossi et al., 2004). These biases affect the interest of the stakeholder. Furthermore, it is possible that program participants are disadvantaged if the bias is in such a way that it contributes to making an ineffective or harmful program seem effective. There is also the possibility that a bias can make an effective program seem ineffective or even as far as harmful. This could possibly make the accomplishments of program seem small or even insignificant therefore forcing the personnel and even cause the program's sponsors to reduce or eliminate the funding for the program (Rossi et al., 2004).
It is safe to say that if an inadequate design yields bias, the stakeholders who are largely responsible for the funding of the program will be the ones most concerned; the results of the evaluation help the stakeholders decide whether or not to continue funding the program because the final decision lies with the funders and the sponsors. Not only are the stakeholders mostly concerned, but those taking part in the program or those the program is intended to positively affect will be affected by the design chosen and the outcome rendered by that chosen design. Therefore, the evaluator's concern is to minimize the amount of bias in the estimation of program effects (Rossi et al., 2004).
Biases are normally visible in two situations: when the measurement of the outcome with program exposure or the estimate of what the outcome would have been without the program exposure is higher or lower than the corresponding "true" value (p267). Unfortunately, not all forms of bias that may compromise impact assessment are obvious (Rossi et al., 2004).
The most common form of impact evaluation design is comparing two groups of individuals or other units, an intervention group that receives the program and a control group that does not. The estimate of program effect is then based on the difference between the groups on a suitable outcome measure (Rossi et al., 2004). The random assignment of individuals to program and control groups allows for making the assumption of continuing equivalence. Group comparisons that have not been formed through randomization are known as non-equivalent comparison designs (Rossi et al., 2004).
Selection bias
[edit]When there is an absence of the assumption of equivalence, the difference in outcome between the groups that would have occurred regardless creates a form of bias in the estimate of program effects. This is known as selection bias (Rossi et al., 2004). It creates a threat to the validity of the program effect estimate in any impact assessment using a non-equivalent group comparison design and appears in situations where some process responsible for influences that are not fully known selects which individuals will be in which group instead of the assignment to groups being determined by pure chance (Rossi et al., 2004). This may be because of participant self-selection, or it may be because of program placement (placement bias).[18]
Selection bias can occur through natural or deliberate processes that cause a loss of outcome data for members of the intervention and control groups that have already been formed. This is known as attrition and it can come about in two ways (Rossi et al., 2004): targets drop out of the intervention or control group cannot be reached or targets refuse to co-operate in outcome measurement. Differential attrition is assumed when attrition occurs as a result of something either than explicit chance process (Rossi et al., 2004). This means that "those individuals that were from the intervention group whose outcome data are missing cannot be assumed to have the same outcome-relevant characteristics as those from the control group whose outcome data are missing" (Rossi et al., 2004, p271). However, random assignment designs are not safe from selection bias which is induced by attrition (Rossi et al., 2004).
Other forms of bias
[edit]There are other factors that can be responsible for bias in the results of an impact assessment. These generally have to do with events or experiences other than receiving the program that occur during the intervention. These biases include secular trends, interfering events and maturation (Rossi et al., 2004).
Secular trends or secular drift
[edit]Secular trends can be defined as being relatively long-term trends in the community, region or country. These are also termed secular drift and may produce changes that enhance or mask the apparent effects of an intervention(Rossi et al., 2004). For example, when a community's birth rate is declining, a program to reduce fertility may appear effective because of bias stemming from that downward trend (Rossi et al., 2004, p273).
Interfering events
[edit]Interfering events are similar to secular trends; in this case it is the short-term events that can produce changes that may introduce bias into estimates of program effect, such as a power outage disrupting communications or hampering the delivery of food supplements may interfere with a nutrition program (Rossi et al., 2004, p273).
Maturation
[edit]Impact evaluation needs to accommodate the fact that natural maturational and developmental processes can produce considerable change independently of the program. Including these changes in the estimates of program effects would result in bias estimates. An example of this form of bias would be a program to improve preventative health practices among adults may seem ineffective because health generally declines with age (Rossi et al., 2004, p273).
"Careful maintenance of comparable circumstances for program and control groups between random assignment and outcome measurement should prevent bias from the influence of other differential experiences or events on the groups. If either of these conditions is absent from the design, there is potential for bias in the estimates of program effect" (Rossi et al., 2004, p274).
Estimation methods
[edit]Estimation methods broadly follow evaluation designs. Different designs require different estimation methods to measure changes in well-being from the counterfactual. In experimental and quasi-experimental evaluation, the estimated impact of the intervention is calculated as the difference in mean outcomes between the treatment group (those receiving the intervention) and the control or comparison group (those who don't). This method is also called randomized control trials (RCT). According to an interview with Jim Rough, former representative of the American Evaluation Association, in the magazine D+C Development and Cooperation, this method does not work for complex, multilayer matters. The single difference estimator compares mean outcomes at end-line and is valid where treatment and control groups have the same outcome values at baseline. The difference-in-difference (or double difference) estimator calculates the difference in the change in the outcome over time for treatment and comparison groups, thus utilizing data collected at baseline for both groups and a second round of data collected at end-line, after implementation of the intervention, which may be years later.[19]
Impact Evaluations which have to compare average outcomes in the treatment group, irrespective of beneficiary participation (also referred to as 'compliance' or 'adherence'), to outcomes in the comparison group are referred to as intention-to-treat (ITT) analyses. Impact Evaluations which compare outcomes among beneficiaries who comply or adhere to the intervention in the treatment group to outcomes in the control group are referred to as treatment-on-the-treated (TOT) analyses. ITT therefore provides a lower-bound estimate of impact, but is arguably of greater policy relevance than TOT in the analysis of voluntary programs.[20]...yes
Debates
[edit]While there is agreement on the importance of impact evaluation, and a consensus is emerging around the use of counterfactual evaluation methods, there has also been widespread debate in recent years on both the definition of impact evaluation and the use of appropriate methods (see White 2009[21] for an overview).
Definitions
[edit]The International Initiative for Impact Evaluation (3ie) defines rigorous impact evaluations as: "analyses that measure the net change in outcomes for a particular group of people that can be attributed to a specific program using the best methodology available, feasible and appropriate to the evaluation question that is being investigated and to the specific context".[22]
According to the World Bank's DIME Initiative, "Impact evaluations compare the outcomes of a program against a counterfactual that shows what would have happened to beneficiaries without the program. Unlike other forms of evaluation, they permit the attribution of observed changes in outcomes to the program being evaluated by following experimental and quasi-experimental designs".[23]
Similarly, according to the US Environmental Protection Agency impact evaluation is a form of evaluation that assesses the net effect of a program by comparing program outcomes with an estimate of what would have happened in the absence of a program.[24]
According to the World Bank's Independent Evaluation Group (IEG), impact evaluation is the systematic identification of the effects positive or negative, intended or not on individual households, institutions, and the environment caused by a given development activity such as a program or project.[25]
Impact evaluation has been defined differently over the past few decades.[6] Other interpretations of impact evaluation include:
- An evaluation which looks at the impact of an intervention on final welfare outcomes, rather than only at project outputs, or a process evaluation which focuses on implementation;
- An evaluation carried out some time (five to ten years) after the intervention has been completed so as to allow time for impact to appear; and
- An evaluation considering all interventions within a given sector or geographical area.
Other authors make a distinction between "impact evaluation" and "impact assessment." "Impact evaluation" uses empirical techniques to estimate the effects of interventions and their statistical significance, whereas "impact assessment" includes a broader set of methods, including structural simulations and other approaches that cannot test for statistical significance.[18]
Common definitions of 'impact' used in evaluation generally refer to the totality of longer-term consequences associated with an intervention on quality-of-life outcomes. For example, the Organization for Economic Cooperation and Development's Development Assistance Committee (OECD-DAC) defines impact as the "positive and negative, primary and secondary long-term effects produced by a development intervention, directly or indirectly, intended or unintended".[26] A number of international agencies have also adopted this definition of impact. For example, UNICEF defines impact as "The longer term results of a program – technical, economic, socio-cultural, institutional, environmental or other – whether intended or unintended. The intended impact should correspond to the program goal."[27] Similarly, Evaluationwiki.org defines impact evaluation as an evaluation that looks beyond the immediate results of policies, instruction, or services to identify longer-term as well as unintended program effects.[28]
Technically, an evaluation could be conducted to assess 'impact' as defined here without reference to a counterfactual. However, much of the existing literature (e.g. NONIE Guidelines on Impact Evaluation[29]) adopts the OECD-DAC definition of impact while referring to the techniques used to attribute impact to an intervention as necessarily based on counterfactual analysis.
What is missing from the term 'impact' evaluation is the way 'impact' shows up long-term. For instance, most Monitoring and Evaluation 'logical framework' plans have inputs-outputs-outcomes and... impacts. While the first three appear during the project duration itself, impact takes far longer to take place. For instance, in a 5-year agricultural project, seeds are inputs, farmers trained in using them our outputs, changes in crop yields as a result of the seeds being planted properly is an outcome and families being more sustainably food secure over time is an impact. Such post-project impact evaluations are very rare. They are also called ex-post evaluations or we are coining the term sustained impact evaluations. While hundreds of thousands of documents call for them, rarely do donors have the funding flexibility - or interest - to return to see how sustained, and durable our interventions remained after project close out, after resources were withdrawn. There are many lessons to be learned for design, implementation, M&E and how to foster country-ownership.
Methodological debates
[edit]There is intensive debate in academic circles around the appropriate methodologies for impact evaluation, between proponents of experimental methods on the one hand and proponents of more general methodologies on the other. William Easterly has referred to this as 'The Civil War in Development economics' Archived 2010-02-06 at the Wayback Machine. Proponents of experimental designs, sometimes referred to as 'randomistas',[8] argue randomization is the only means to ensure unobservable selection bias is accounted for, and that building up the flimsy experimental evidence base should be developed as a matter of priority.[30] In contrast, others argue that randomized assignment is seldom appropriate to development interventions and even when it is, experiments provide us with information on the results of a specific intervention applied to a specific context, and little of external relevance.[31] There has been criticism from evaluation bodies and others that some donors and academics overemphasize favoured methods for impact evaluation,[32] and that this may in fact hinder learning and accountability.[33] In addition, there has been a debate around the appropriate role for qualitative methods within impact evaluations.[34][35]
Theory-based impact evaluation
[edit]While knowledge of effectiveness is vital, it is also important to understand the reasons for effectiveness and the circumstances under which results are likely to be replicated. In contrast with 'black box' impact evaluation approaches, which only report mean differences in outcomes between treatment and comparison groups, theory-based impact evaluation involves mapping out the causal chain from inputs to outcomes and impact and testing the underlying assumptions.[36][29] Most interventions within the realm of public policy are of a voluntary, rather than coercive (legally required) nature. In addition, interventions are often active rather than passive, requiring a greater rather than lesser degree of participation among beneficiaries and therefore behavior change as a pre-requisite for effectiveness. Public policy will therefore be successful to the extent that people are incentivized to change their behaviour favourably. A theory-based approach enables policy-makers to understand the reasons for differing levels of program participation (referred to as 'compliance' or 'adherence') and the processes determining behavior change. Theory-Based approaches use both quantitative and qualitative data collection, and the latter can be particularly useful in understanding the reasons for compliance and therefore whether and how the intervention may be replicated in other settings. Methods of qualitative data collection include focus groups, in-depth interviews, participatory rural appraisal (PRA) and field visits, as well as reading of anthropological and political literature.
White (2009b)[36] advocates more widespread application of a theory-based approach to impact evaluation as a means to improve policy relevance of impact evaluations, outlining six key principles of the theory-based approach:
- Map out the causal chain (program theory) which explains how the intervention is expected to lead to the intended outcomes, and collect data to test the underlying assumptions of the causal links.
- Understand context, including the social, political and economic setting of the intervention.
- Anticipate heterogeneity to help in identifying sub-groups and adjusting the sample size to account for the levels of disaggregation to be used in the analysis.
- Rigorous evaluation of impact using a credible counterfactual (as discussed above).
- Rigorous factual analysis of links in the causal chain.
- Use mixed methods (a combination of quantitative and qualitative methods).
Examples
[edit]While experimental impact evaluation methodologies have been used to assess nutrition and water and sanitation interventions in developing countries since the 1980s, the first, and best known, application of experimental methods to a large-scale development program is the evaluation of the Conditional Cash Transfer (CCT) program Progresa (now called Oportunidades) in Mexico, which examined a range of development outcomes, including schooling, immunization rates and child work.[37][38] CCT programs have since been implemented by a number of governments in Latin America and elsewhere, and a report released by the World Bank in February 2009 examines the impact of CCTs across twenty countries.[39]
More recently, impact evaluation has been applied to a range of interventions across social and productive sectors. 3ie has launched an online database of impact evaluations[permanent dead link] covering studies conducted in low- and middle income countries. Other organisations publishing Impact Evaluations include Innovations for Poverty Action, the World Bank's DIME Initiative and NONIE. The IEG of the World Bank has systematically assessed and summarized the experience of ten impact evaluation of development programs in various sectors carried out over the past 20 years.[40]
Organizations promoting impact evaluation of development interventions
[edit]In 2006, the Evaluation Gap Working Group[41] argued for a major gap in the evidence on development interventions, and in particular for an independent body to be set up to plug the gap by funding and advocating for rigorous impact evaluation in low- and middle-income countries. The International Initiative for Impact Evaluation (3ie) was set up in response to this report. 3ie seeks to improve the lives of poor people in low- and middle-income countries by providing, and summarizing, evidence of what works, when, why and for how much. 3ie operates a grant program, financing impact studies in low- and middle-income countries and synthetic reviews of existing evidence updated as new evidence appears, and supports quality impact evaluation through its quality assurance services.
Another initiative devoted to the evaluation of impacts is the Committee on Sustainability Assessment (COSA). COSA is a non-profit global consortium of institutions, sustained in partnership with the International Institute for Sustainable Development (IISD) Sustainable Commodity Initiative, the United Nations Conference on Trade and Development (UNCTAD), and the United Nations International Trade Centre (ITC). COSA is developing and applying an independent measurement tool to analyze the distinct social, environmental and economic impacts of agricultural practices, and in particular those associated with the implementation of specific sustainability programs (Organic, Fairtrade etc.). The focus of the initiative is to establish global indicators and measurement tools which farmers, policy-makers, and industry can use to understand and improve their sustainability with different crops or agricultural sectors. COSA aims to facilitate this by enabling them to accurately calculate the relative costs and benefits of becoming involved in any given sustainability initiative.
A number of additional organizations have been established to promote impact evaluation globally, including Innovations for Poverty Action, the World Bank's Strategic Impact Evaluation Fund (SIEF), the World Bank's Development Impact Evaluation (DIME) Initiative, the Institutional Learning and Change (ILAC) Initiative of the CGIAR, and the Network of Networks on Impact Evaluation (NONIE).
Systematic reviews of impact evidence
[edit]A range of organizations are working to coordinate the production of systematic reviews. Systematic reviews aim to bridge the research-policy divide by assessing the range of existing evidence on a particular topic, and presenting the information in an accessible format. Like rigorous impact evaluations, they are developed from a study Protocol which sets out a priori the criteria for study inclusion, search and methods of synthesis. Systematic reviews involve five key steps: determination of interventions, populations, outcomes and study designs to be included; searches to identify published and unpublished literature, and application of study inclusion criteria (relating to interventions, populations, outcomes and study design), as set out in study Protocol; coding of information from studies; presentation of quantitative estimates on intervention effectiveness using forest plots and, where interventions are determined as appropriately homogeneous, calculation of a pooled summary estimate using meta-analysis; finally, systematic reviews should be updated periodically as new evidence emerges. Systematic reviews may also involve the synthesis of qualitative information, for example relating to the barriers to, or facilitators of, intervention effectiveness.
See also
[edit]References
[edit]- ^ World Bank Poverty Group on Impact Evaluation, accessed on January 6, 2008
- ^ "White, H. (2006) Impact Evaluation: The Experience of the Independent Evaluation Group of the World Bank, World Bank, Washington, D.C., p. 3" (PDF). Archived from the original (PDF) on 2018-02-19. Retrieved 2010-01-07.
- ^ "Gertler, Martinez, Premand, Rawlings and Vermeersch (2011) Impact Evaluation in Practice, Washington, DC:The World Bank". Archived from the original on 2011-07-17. Retrieved 2010-12-15.
- ^ "Log in" (PDF). Retrieved 16 January 2017.
- ^ "Log in" (PDF). Retrieved 16 January 2017.
- ^ a b "White, H. (2006) Impact Evaluation: The Experience of the Independent Evaluation Group of the World Bank, World Bank, Washington, D.C." (PDF). Archived from the original (PDF) on 2018-02-19. Retrieved 2010-01-07.
- ^ Ravallion, M. (2008) Evaluating Anti-Poverty Programs
- ^ a b Martin, Ravallion (1 January 2009). "Should the Randomistas Rule?". 6 (2): 1–5. Retrieved 16 January 2017 – via RePEc - IDEAS.
{{cite journal}}: Cite journal requires|journal=(help) - ^ Note that it has been argued that “Randomistas is a slang term used by critics to describe proponents of the RCT methodology. It is almost certainly a gendered, derogatory term intended to flippantly dismiss experimental economists and their success, particularly Esther Duflo, one of the most successful experts on randomization.” See Webber, S., & Prouse, C. (2018). The New Gold Standard: The Rise of Randomized Control Trials and Experimental Development. Economic Geography, 94(2), 166–187.
- ^ a b Bamberger, M. and White, H. (2007) Using Strong Evaluation Designs in Developing Countries: Experience and Challenges, Journal of MultiDisciplinary Evaluation, Volume 4, Number 8, 58-73
- ^ Scriven (2008) A Summative Evaluation of RCT Methodology: & An Alternative Approach to Causal Research, Journal of MultiDisciplinary Evaluation, Volume 5, Number 9, 11-24
- ^ Deaton, Angus (1 January 2009). "Instruments of Development: Randomization in the Tropics, and the Search for the Elusive Keys to Economic Development". SSRN 1335715.
{{cite journal}}: Cite journal requires|journal=(help) - ^ Hariton, Eduardo; Locascio, Joseph J. (December 2018). "Randomised controlled trials—the gold standard for effectiveness research". BJOG: An International Journal of Obstetrics and Gynaecology. 125 (13): 1716. doi:10.1111/1471-0528.15199. ISSN 1470-0328. PMC 6235704. PMID 29916205.
- ^ a b White, Howard (8 March 2013). "An introduction to the use of randomised control trials to evaluate development interventions". Journal of Development Effectiveness. 5: 30–49. doi:10.1080/19439342.2013.764652. S2CID 51812043.
- ^ a b Deaton, Angus; Cartwright, Nancy (2016-11-09). "The limitations of randomised controlled trials". VoxEU.org. Retrieved 2020-10-26.
- ^ a b c Roe, Brian E.; Just, David R. (December 2009). "Internal and External Validity in Economics Research: Tradeoffs between Experiments, Field Experiments, Natural Experiments, and Field Data". American Journal of Agricultural Economics. 91 (5): 1266–1271. doi:10.1111/j.1467-8276.2009.01295.x. hdl:10.1111/j.1467-8276.2009.01295.x. ISSN 0002-9092.
- ^ Callaway, Brantly; Sant’Anna, Pedro H. C. (2021-12-01). "Difference-in-Differences with multiple time periods". Journal of Econometrics. Themed Issue: Treatment Effect 1. 225 (2): 200–230. doi:10.1016/j.jeconom.2020.12.001. ISSN 0304-4076.
- ^ a b White, Howard; Raitzer, David (2017). Impact Evaluation of Development Interventions: A Practical Guide (PDF). Manila: Asian Development Bank. ISBN 978-92-9261-059-3.
- ^ Rugh, Jim (June 22, 2012). "Hammer in search of nails". D+C Development and Cooperation. 2012 (7): 300.
- ^ Bloom, H. (2006) The core analytics of randomized experiments for social research. MDRC Working Papers on Research Methodology. MDRC, New York
- ^ "White, H. (2009) Some reflections on current debates in impact evaluation, Working paper 1, International Initiative for Impact Evaluation, New Delhi". Archived from the original on 2013-01-08. Retrieved 2012-10-29.
- ^ "Log in" (PDF). Retrieved 16 January 2017.
- ^ World Bank (n.d.) The Development IMpact Evaluation (DIME) Initiative, Project Document, World Bank, Washington, D.C.
- ^ US Environmental Protection Agency Program Evaluation Glossary, accessed on January 6, 2008
- ^ World Bank Independent Evaluation Group, accessed on January 6, 2008
- ^ OECD-DAC (2002) Glossary of Key Terms in Evaluation and Results-Based Management Proposed Harmonized Terminology, OECD, Paris
- ^ UNICEF (2004) UNICEF Evaluation Report Standards, Evaluation Office, UNICEF NYHQ, New York
- ^ "Evaluation Definition: What is Evaluation? - EvaluationWiki". Retrieved 16 January 2017.[permanent dead link]
- ^ a b "Page Not Found". Retrieved 16 January 2017.
{{cite web}}: Cite uses generic title (help) - ^ "Banerjee, A. V. (2007) 'Making Aid Work' Cambridge, Boston Review Book, MIT Press, MA" (PDF). Retrieved 16 January 2017.[permanent dead link]
- ^ Bamberger, M. and White, H. (2007) Using Strong Evaluation Designs in Developing Countries: Experience and Challenges, Journal of MultiDisciplinary Evaluation, Volume 4, Number 8, 58-73
- ^ http://www.europeanevaluation.org/download/?noGzip=1&id=1969403[permanent dead link] EES Statement on the importance of a methodologically diverse approach to impact evaluation
- ^ http://www.odi.org.uk/resources/odi-publications/opinions/127-impact-evaluation.pdf[permanent dead link] The 'gold standard' is not a silver bullet for evaluation
- ^ "Aid effectiveness: The role of qualitative research in impact evaluation". 27 June 2014.
- ^ Prowse, Martin; Camfield, Laura (2013). "Improving the quality of development assistance". Progress in Development Studies. 13: 51–61. doi:10.1177/146499341201300104. S2CID 44482662.
- ^ a b "White, H. (2009b) Theory-based impact evaluation: Principles and practice, Working Paper 3, International Initiative for Impact Evaluation, New Delhi". Archived from the original on 2012-11-06. Retrieved 2012-10-29.
- ^ Gertler, P. (2000) Final Report: The Impact of PROGRESA on Health. International Food Policy Research Institute, Washington, D.C.
- ^ "Untitled Document" (PDF). Retrieved 16 January 2017.
- ^ Fiszbein, A. and Schady, N. (2009) Conditional Cash Transfers: Reducing present and future poverty: A World Bank Policy Research Report, World Bank, Washington, D.C.
- ^ "Impact Evaluation: The Experience of the Independent Evaluation Group of the World Bank, 2006" (PDF). Archived from the original (PDF) on 2008-05-10. Retrieved 2008-01-07.
- ^ "When Will We Ever Learn? Improving Lives Through Impact Evaluation". 31 May 2006. Retrieved 16 January 2017.
Impact evaluation
View on GrokipediaDefinition and Fundamentals
Core Concepts and Purpose
Impact evaluation entails the rigorous estimation of causal effects attributable to an intervention, program, or policy on targeted outcomes, achieved by comparing observed results against the counterfactual—what outcomes would have prevailed absent the intervention.[10][11] This approach distinguishes impact from mere correlation by addressing the fundamental identification problem: the counterfactual remains inherently unobservable, necessitating empirical strategies to approximate it, such as randomization or statistical matching to construct comparable control groups.[12] Central concepts include the average treatment effect (ATE), which quantifies the mean difference in outcomes between treated and untreated units, and considerations of heterogeneity, where effects may vary across subgroups, contexts, or over time.[13] The purpose of impact evaluation lies in generating credible evidence to ascertain whether interventions produce net benefits, the scale of those benefits, and the conditions under which they occur, thereby enabling data-driven decisions in resource-constrained environments.[14] In development contexts, it supports the prioritization of effective programs to alleviate poverty and enhance welfare, as scarce public funds demand verification that expenditures yield measurable improvements rather than illusory gains from confounding factors.[14] Beyond accountability, it informs program refinement, scalability assessments, and policy replication, countering reliance on anecdotal or associational evidence that often overstates efficacy due to omitted variables or selection effects.[15] Evaluations thus promote causal realism, emphasizing mechanisms linking inputs to outputs while highlighting failures, such as null or adverse effects, to avoid perpetuating ineffective practices.[12]Historical Origins and Evolution
The systematic assessment of program impacts, particularly through causal inference, originated in early quantitative evaluation practices but gained methodological rigor in the mid-20th century. Initial roots lie in 19th-century reforms, including William Farish's 1792 introduction of numerical marks for academic performance at Cambridge University and Horace Mann's 1845 standardized tests in Boston schools to gauge educational effectiveness. These efforts focused on measurement for accountability rather than causality. By the early 20th century, Frederick W. Taylor's scientific management principles (circa 1911) emphasized efficiency metrics, evolving into objective testing movements that laid groundwork for outcome-oriented scrutiny, though without robust controls for confounding factors.[16] The modern era of impact evaluation emerged in the 1950s-1960s, driven by post-World War II expansions in education and social welfare programs, including the U.S. National Defense Education Act (1958) and Elementary and Secondary Education Act (1965), which mandated evaluations amid concerns over program efficacy. The Sputnik launch in 1957 heightened demands for evidence-based policy, while the Great Society initiatives spurred social experiments to test interventions like income support. Donald T. Campbell and Julian C. Stanley's 1963 monograph Experimental and Quasi-Experimental Designs for Research formalized designs to mitigate internal validity threats—such as selection bias and maturation—in non-laboratory settings, enabling causal claims from observational data approximations like pre-post comparisons and nonequivalent control groups. This framework professionalized evaluation, distinguishing true experiments from quasi-experiments and influencing fields beyond psychology.[17][18] Pioneering randomized controlled trials (RCTs) in social policy followed, with the U.S. Negative Income Tax experiments (1968-1982) randomizing households to assess guaranteed income effects on labor supply, and the RAND Health Insurance Experiment (1971-1982) evaluating cost-sharing's impact on healthcare utilization, informing 1980s policy shifts toward deductibles. In international development, Mexico's PROGRESA conditional cash transfer program (1997) employed RCTs to measure effects on school enrollment and health, catalyzing scalable evaluations across Latin America and beyond.[19][20] The 2000s marked explosive evolution, termed the "evidence revolution," with institutions like the Abdul Latif Jameel Poverty Action Lab (J-PAL, founded 2003) and the International Initiative for Impact Evaluation (3ie, 2008) institutionalizing RCTs and quasi-experimental methods for poverty alleviation. The U.S. Government Performance and Results Act (1993) and UK Modernizing Government initiative (1999) embedded outcome-focused evaluation in public administration. Advances integrated econometric tools, such as instrumental variables and regression discontinuity designs, to handle endogeneity in large-scale data. This period's emphasis on rigorous causality peaked with the 2019 Nobel Prize in Economics awarded to Abhijit Banerjee, Esther Duflo, and Michael Kremer for RCTs demonstrating interventions' micro-level effects on development outcomes. Subsequent growth includes evidence synthesis via systematic reviews and government-embedded labs, though debates persist over generalizability from small-scale trials to policy scale.[19][21]Methodological Designs
Experimental Designs
Experimental designs in impact evaluation primarily utilize randomized controlled trials (RCTs), in which eligible units such as individuals, households, or communities are randomly assigned to treatment (receiving the intervention) or control (no intervention) groups to isolate causal effects from confounding factors.[22][23] This random assignment, typically executed through computer algorithms or lotteries, ensures that groups are statistically equivalent on average, both in observed covariates and unobserved characteristics, allowing outcome differences to be credibly attributed to the intervention.[23] RCTs thus provide unbiased estimates of the average treatment effect (ATE), addressing the fundamental challenge of counterfactual reasoning—what would have happened without the intervention—by using the control group as a proxy.[22] Key steps in RCT design include defining the eligible population, conducting power calculations to determine required sample size based on expected effect sizes and variability (often aiming for 80% power to detect minimum detectable effects), and verifying post-randomization balance through statistical tests on baseline data.[22] Outcomes are measured via surveys, administrative records, or other instruments at baseline and endline, with analysis focusing on intent-to-treat (ITT) effects—comparing groups as randomized—to maintain randomization integrity, or treatment-on-the-treated (TOT) effects using instruments for compliance issues.[23] Regression models may adjust for covariates to increase precision, though unadjusted differences suffice for primary inference under randomization.[22] Variations adapt RCTs to contextual constraints. Individual-level randomization assigns treatment independently to each unit, maximizing statistical power but risking spillovers in interconnected settings.[22] Cluster-randomized trials, conversely, assign intact groups (e.g., villages or schools) to treatment or control, mitigating interference while requiring larger samples and intra-cluster correlation adjustments; for example, Mexico's PROGRESA program randomized 506 communities to evaluate conditional cash transfers, demonstrating sustained impacts on school enrollment.[23][22] Factorial designs test multiple interventions simultaneously by crossing treatment arms (e.g., combining cash transfers with training), enabling assessment of interactions and main effects within one trial, as in variations of Indonesia's Raskin food subsidy program across 17.5 million beneficiaries in 2012.[23][24] Stratified or blocked randomization ensures balance across subgroups like gender or location, enhancing precision without altering causal identification.[22] Staggered or phase-in designs roll out interventions sequentially, using early phases as controls for later ones in scalable programs.[23] These designs prioritize internal validity but demand safeguards against threats like spillovers (intervention diffusion to controls) or crossovers (controls accessing treatment), addressed via geographic separation or monitoring.[22] Ethical implementation requires uncertainty about intervention efficacy and minimal harm from control withholding, often justified by potential phase-in for all post-evaluation.[23] Empirical evidence from RCTs, such as a 43% reduction in violent crime arrests from Chicago's One Summer Plus job program, underscores their capacity for policy-relevant causal insights when properly executed.[23]Quasi-Experimental and Observational Designs
Quasi-experimental designs estimate causal impacts of interventions without random assignment, relying instead on structured comparisons or natural variations to approximate experimental conditions. These approaches, first systematically outlined by Donald T. Campbell and Julian C. Stanley in their 1963 chapter, address threats to internal validity through designs like time-series analyses or nonequivalent control groups, enabling inference in real-world settings where randomization is infeasible, such as policy implementations or large-scale programs.[25][26] Unlike true experiments, they demand explicit assumptions—such as the absence of contemporaneous events affecting groups differentially—to isolate treatment effects, with validity often assessed via placebo tests or falsification strategies. A core quasi-experimental method is difference-in-differences (DiD), which identifies impacts by subtracting pre-treatment outcome differences from post-treatment differences between treated and control groups, under the parallel trends assumption that untreated trends would mirror counterfactuals. Applied in evaluations like the 1996 U.S. welfare reform, DiD has shown, for instance, that job training programs increased earnings by 10-20% in some cohorts when controlling for economic cycles.[27][28] Extensions, such as triple differences, incorporate additional dimensions like geography to mitigate violations from heterogeneous trends, though recent critiques highlight sensitivity to staggered adoption in multi-period settings.[29] Regression discontinuity designs (RDD) exploit deterministic assignment rules, estimating local average treatment effects from outcome discontinuities at a cutoff, where units near the threshold are quasi-randomized by the forcing variable. In a 2013 evaluation of Colombia's Ser Pilo Paga scholarship, RDD revealed a 0.17 standard deviation increase in college enrollment for score-justifiers above the eligibility line, with bandwidth selection via optimal methods ensuring precise local inference.[30] Sharp RDD assumes perfect compliance at the cutoff, while fuzzy variants handle partial take-up using IV within the framework; both require checks for manipulation, such as density tests showing no bunching.[31] Instrumental variables (IV) address endogeneity by using an exogenous instrument correlated with treatment uptake but unrelated to outcomes except through treatment, yielding estimates for compliers under monotonicity. In Angrist and Krueger's 1991 analysis of U.S. compulsory schooling, quarter-of-birth instruments—leveraging school entry age laws—estimated a 7-10% return to an additional year of education, isolating causal effects amid self-selection.[32] Instrument validity hinges on relevance (strong first-stage correlation) and exclusion (no direct outcome path), tested via overidentification in multiple-IV setups; weak instruments bias estimates toward OLS, as quantified in Stock-Yogo critical values from 2005.[33] Observational designs draw causal inferences from non-manipulated data, emphasizing conditional independence or structural assumptions to mitigate confounding, often via balancing methods like propensity score matching (PSM), which estimates treatment probabilities from covariates to pair similar units. A 2023 review found PSM effective in observational evaluations of public health interventions, reducing bias by up to 80% when overlap is sufficient, though it fails with unobservables, as evidenced by simulation studies showing 20-50% attenuation under hidden confounders.[34][35] Advanced observational techniques include panel fixed effects, which difference out time-invariant confounders in longitudinal data, and synthetic controls, constructing counterfactuals as weighted untreated unit combinations to match pre-treatment trajectories. In Abadie et al.'s 2010 California tobacco control evaluation, synthetic controls attributed a 20-30% drop in per-capita cigarettes to the policy, outperforming simple DiD under heterogeneous trends.[36] These methods demand large samples and covariate balance diagnostics, with triangulation—combining, say, PSM and IV—enhancing robustness, as recommended in 2021 guidelines for non-randomized studies.[37] Despite strengths in scalability, observational designs remain vulnerable to model misspecification, necessitating pre-registration and falsification tests to approximate causal credibility.[38]Sources of Bias and Validity Threats
Selection and Attrition Biases
Selection bias occurs when systematic differences between treatment and comparison groups arise due to non-random assignment or participation, leading to distorted estimates of causal effects in impact evaluations. In observational or quasi-experimental designs, individuals self-selecting into programs often possess unobserved characteristics—such as motivation or ability—that correlate with outcomes, inflating or deflating apparent program impacts; for instance, remaining selection bias after matching techniques can exceed 100% of the experimentally estimated effect in social program evaluations.[39] This threat undermines internal validity by violating the assumption of exchangeability between groups, making it challenging to attribute outcome differences solely to the intervention rather than pre-existing disparities.[40] Even in randomized controlled trials (RCTs), selection bias can emerge if eligibility criteria or recruitment processes favor certain subgroups, though proper randomization typically mitigates it at baseline.[41] Attrition bias, a post-randomization form of selection bias, arises when participants exit studies at differential rates between treatment and control groups, particularly if dropouts are correlated with outcomes or treatment status, thereby altering group compositions and biasing effect estimates. In RCTs for social programs, such as early childhood interventions, attrition rates exceeding 20% often introduce systematic imbalances, with leavers in treatment groups potentially having worse outcomes than stayers, leading to overestimation of positive effects if not addressed.[42][43] This bias threatens the completeness of intention-to-treat analyses and can amplify in longitudinal evaluations where follow-up surveys fail to retain high-risk participants, as seen in teen pregnancy prevention trials where cluster-level attrition exacerbates imbalances.[44] Unlike baseline selection, attrition introduces time-varying confounding, as dropout reasons—like program dissatisfaction or external shocks—may interact with treatment exposure.[45] Both biases compromise causal inference by eroding the comparability of groups essential for counterfactual estimation; selection operates pre-treatment, while attrition does so post-treatment, but they converge in non-random loss of data that correlates with potential outcomes. In development impact evaluations, empirical assessments show that unadjusted attrition can shift effect sizes by 10-30% in magnitude, with bounding approaches or sensitivity analyses revealing the direction of potential distortion.[46] Mitigation strategies include baseline covariates for reweighting, worst-case scenario bounds, or pattern-mixture models, though these require assumptions about missingness mechanisms that may not hold without auxiliary data. High-quality evaluations report attrition rates and test for baseline differences among dropouts to quantify threats, emphasizing that low attrition alone does not guarantee unbiasedness if patterns are non-ignorable.[47][48]Temporal and Contextual Biases
Temporal biases in impact evaluation refer to systematic errors introduced by time-related factors that confound causal attribution, often threatening internal validity by providing alternative explanations for observed changes in outcomes. History effects occur when external events, unrelated to the intervention, coincide with its implementation and influence results; for instance, a concurrent economic policy change might inflate estimates of a job training program's employment effects. Maturation effects arise from natural developmental or aging processes in participants, such as improved cognitive skills in children over the study period, which could be mistakenly attributed to an educational intervention.[49][50] These biases are particularly pronounced in longitudinal or quasi-experimental designs lacking randomization, where pre-intervention trends or secular drifts—broader societal shifts like technological adoption—may parallel the treatment timeline and bias impact estimates upward or downward. Regression to the mean exacerbates temporal issues when extreme baseline values naturally moderate over time, as seen in evaluations of interventions targeting high-risk groups, such as substance abuse programs where initial severity scores revert without treatment influence. To mitigate, evaluators often employ difference-in-differences methods to test parallel trends or include time-fixed effects in models.[49][51] Contextual biases stem from the specific setting or environment of the evaluation, which can modify intervention effects or introduce local confounders, thereby limiting generalizability and introducing effect heterogeneity. Interaction effects with settings manifest when outcomes vary due to unmeasured site-specific factors, such as cultural norms or institutional support; for example, a microfinance program's success in rural areas may not replicate in urban contexts due to differing market dynamics. Spillover effects, where treatment benefits leak to controls within the same locale, contaminate comparisons, as documented in cluster-randomized trials of health interventions where community-level diffusion biases null findings toward underestimation.[49][50] Hawthorne effects represent a reactive contextual bias, wherein participants alter behavior due to awareness of evaluation, inflating impacts in monitored settings like workplace productivity studies. Site selection bias further compounds issues when programs are evaluated in non-representative locations correlated with higher efficacy, such as motivated communities, leading to overoptimistic extrapolations. Addressing these requires explicit testing for moderators via subgroup analyses or heterogeneous treatment effect estimators, alongside transparent reporting of contextual descriptors to aid external validity assessments.[49][52]Estimation and Analytical Techniques
Causal Inference Methods
Causal inference methods in impact evaluation seek to identify and quantify the effects of interventions by estimating counterfactual outcomes, typically under the potential outcomes framework. This framework posits that for each unit , there exist two potential outcomes: under treatment and under control, with the individual treatment effect defined as .[53] The average treatment effect (ATE) averages this difference across units, but the fundamental challenge arises because only one outcome is observed per unit, necessitating assumptions to link observables to the unobserved counterfactual.[54] Originating from Neyman's work in randomized experiments (1923) and extended by Rubin (1974) to broader settings, the framework underpins modern quasi-experimental estimation by emphasizing identification via conditional independence or exclusion restrictions.[4] These methods are particularly vital in observational data from impact evaluations, where randomization is absent, requiring strategies to mimic experimental conditions through covariates, instruments, or discontinuities. Common approaches include propensity score matching, instrumental variables, regression discontinuity, and difference-in-differences, each relying on distinct identifying assumptions to bound or point-identify causal effects. While powerful, their validity hinges on untestable assumptions, such as no unmeasured confounders or parallel trends, which empirical checks like placebo tests or sensitivity analyses can probe but not fully verify.[3] Propensity Score Matching (PSM) balances treated and control groups by matching on the propensity score, defined as the probability of treatment given observed covariates , . Under selection on observables (conditional independence: ), matching yields unbiased estimates of the ATE for the treated or overall. Introduced by Rosenbaum and Rubin (1983), PSM reduces dimensionality from multiple covariates to one score, often implemented via nearest-neighbor or kernel matching, with caliper restrictions to ensure close matches.[55] In impact evaluations of social programs, such as job training initiatives, PSM has estimated effects like a 10-20% earnings increase from participation, though it fails if unobservables like motivation confound assignment.[4] Sensitivity to model misspecification and common support violations necessitates balance diagnostics, where covariate means post-matching should align across groups. Instrumental Variables (IV) addresses endogeneity from unobservables by leveraging an instrument correlated with treatment (relevance: ) but affecting outcomes only through (exclusion: no direct path from to ). The two-stage least squares (2SLS) estimator recovers the local average treatment effect (LATE) for compliers—those whose treatment status changes with —under monotonicity (no defiers). Angrist, Imbens, and Rubin (1996) formalized LATE as the relevant parameter when heterogeneity exists, applied in evaluations like quarter-of-birth instruments for schooling returns, yielding IV estimates of 7-10% per year of education versus 5-8% from OLS. Weak instruments bias estimates toward OLS (first-stage F-statistic >10 recommended), and exclusion violations, such as spillover effects, undermine credibility; overidentification tests (Sargan-Hansen) assess multiple instruments.[56] Regression Discontinuity Design (RDD) exploits sharp or fuzzy discontinuities at a known cutoff in the assignment rule, treating units just above and below as locally randomized. In sharp RDD, the treatment effect is the jump in the conditional expectation of at the cutoff, estimated via local polynomials or parametric regressions with bandwidth selection (e.g., Imbens-Kalyanaraman optimal). Imbens and Lemieux (2008) outline implementation, including density tests for manipulation and placebo outcomes for bandwidth sensitivity.[57] For policy cutoffs like scholarships at exam score thresholds, RDD has quantified effects such as a 0.2-0.5 standard deviation improvement in future earnings, with internal validity strongest near the cutoff but external validity limited to that margin. Fuzzy RDD extends to imperfect compliance using IV logic, where the first-stage discontinuity instruments the treatment probability.[58] Difference-in-Differences (DiD) estimates effects by differencing changes in outcomes over time between treated and control groups, identifying the ATE under parallel trends: absent treatment, gaps would evolve similarly. The estimator is , where subscripts denote treated/ control and post/pre periods. Bertrand, Duflo, and Mullainathan (2004) highlight serial correlation inflating standard errors in multi-period panels, recommending clustered errors or data collapse to two periods for robustness.[59] In evaluations of minimum wage hikes, DiD has shown null or small employment effects (e.g., -0.1% per 10% wage increase), contrasting event-study pre-trends to validate assumptions.[60] Extensions like triple differences add a third dimension to control fixed differences, but violations from differential shocks (e.g., Ashenfelter dips) require synthetic controls or staggered adoption adjustments. Other techniques, such as synthetic control for aggregate interventions, construct counterfactuals as weighted combinations of untreated units matching pre-treatment trends, effective for rare events like policy reforms in single units.[4] Across methods, robustness checks, including placebo applications and falsification on pre-treatment data, are essential, as are meta-analyses revealing that quasi-experimental estimates often align with RCTs when assumptions hold, though divergence signals bias.[3] Integration with machine learning for covariate adjustment or double robustness (combining outcome and propensity models) enhances precision but demands large samples to avoid overfitting.[61]Economic Evaluation Integration
Economic evaluation integration in impact evaluation extends causal effect estimation by incorporating cost data to assess resource efficiency, enabling comparisons of interventions' value relative to alternatives. This approach quantifies whether observed impacts justify expended resources, often through metrics like incremental cost-effectiveness ratios (ICERs) or benefit-cost ratios (BCRs). For instance, in development programs, impact evaluations using randomized controlled trials (RCTs) may pair treatment effect estimates on outcomes such as school enrollment with program delivery costs to compute costs per additional enrollee.[62] Such integration supports decision-making on scaling interventions, as seen in analyses by organizations like the International Initiative for Impact Evaluation (3ie), which emphasize prospective cost data collection alongside experimental designs to avoid retrospective biases.[62] Cost-effectiveness analysis (CEA), a primary method, measures the cost per unit of outcome achieved, such as dollars per life-year saved or per child educated, without requiring full monetization of benefits. In RCT-based impact evaluations, CEA typically applies the intervention's average cost per beneficiary to the estimated average treatment effect, yielding ratios like $X per Y% increase in productivity.[63] A 2024 3ie handbook outlines standardized steps for CEA in impact evaluations, including delineating direct and indirect costs (e.g., staff time, materials, overhead) and sensitivity analyses for uncertainty in effect sizes or cost estimates.[62] Challenges include attributing shared costs in multi-component interventions and using shadow prices for non-traded inputs in low-income settings, where market prices may distort true opportunity costs.[64] Cost-benefit analysis (CBA) advances further by monetizing all outcomes, comparing discounted streams of benefits against costs to derive net present values or internal rates of return. Applied to impact evaluations, CBA requires valuing non-market effects, such as health improvements via willingness-to-pay proxies or human capital models projecting lifetime earnings gains from education interventions.[65] A World Bank analysis found that fewer than 20% of impact evaluations incorporate CBA, often due to data demands and methodological debates over valuation assumptions, yet those that do reveal high returns, like BCRs exceeding 5:1 for deworming programs in Kenya based on long-term income effects.[64][65] Integration with quasi-experimental designs demands adjustments for selection biases in cost attribution, using techniques like propensity score matching to estimate counterfactual costs.[66] Despite advantages, integration faces institutional barriers, including underinvestment in cost data collection during trials, where focus prioritizes statistical significance of impacts over economic metrics.[63] Guidelines from bodies like the World Bank advocate embedding economic components from study inception, with prospective costing protocols to capture fixed and variable expenses accurately.[64] Empirical evidence from development economics underscores the policy relevance, as integrated evaluations have informed reallocations, such as prioritizing cash transfers over less cost-effective subsidies when BCRs differ by factors of 2-10.[65] Ongoing refinements address generalizability, incorporating transferability adjustments for context-specific costs and effects across settings.[62]Debates and Methodological Controversies
RCT Gold Standard vs. Alternative Approaches
Randomized controlled trials (RCTs) are widely regarded as the gold standard in impact evaluation for establishing causal effects due to randomization, which balances treatment and control groups on both observed and unobserved confounders, thereby minimizing selection bias and enabling unbiased estimates of average treatment effects under ideal conditions.[67] This approach has been particularly influential in fields like development economics, where organizations such as J-PAL have scaled RCTs to evaluate interventions like deworming programs, yielding precise estimates of effects such as a 0.14 standard deviation increase in earnings from childhood deworming in Kenya as of long-term follow-ups reported in 2019.[68] However, proponents acknowledge that RCTs assume stable mechanisms and no spillover effects, which may not hold in complex social settings. Despite their strengths in internal validity, RCTs face significant limitations that challenge their unqualified status as the gold standard. Ethical constraints prevent randomization in many policy contexts, such as evaluating universal programs like national education reforms, while high costs—often exceeding $1 million per trial in development settings—and long timelines limit scalability.[69] External validity is another concern, as RCT participants and settings are often unrepresentative; for instance, trials in controlled environments may overestimate effects in diverse real-world applications, with meta-analyses showing effect sizes in RCTs decaying by up to 50% when scaled up.[70] Critics like Angus Deaton argue that RCTs provide narrow, context-specific knowledge without illuminating underlying mechanisms or generalizability, potentially misleading policy if treated as universally superior evidence, as evidenced by discrepancies between RCT findings and broader econometric data in poverty alleviation studies.[68] Alternative approaches, particularly quasi-experimental designs, offer robust causal inference when RCTs are infeasible by exploiting natural or policy-induced variation. Methods like regression discontinuity designs (RDD) assign treatment based on a cutoff score, approximating randomization near the threshold; for example, an RDD evaluation of Colombia's scholarship program in 2012 estimated a 4.8 percentage point increase in college enrollment, comparable to RCT benchmarks.[71] Difference-in-differences (DiD) compares changes over time between treated and untreated groups assuming parallel trends, as in Card and Krueger's 1994 minimum wage study, which found no employment loss in New Jersey fast-food sectors post-1992 hike.[72] Instrumental variables (IV) use exogenous shocks for identification, addressing endogeneity in observational data. These methods rely on testable assumptions—such as no anticipation in RDD or parallel trends in DiD—allowing empirical validation, and often provide stronger external validity by leveraging large-scale administrative data rather than small, artificial samples.[73] The debate pits RCT advocates, including Joshua Angrist and Guido Imbens—who emphasize randomization's avoidance of model dependence against alternatives' reliance on untestable assumptions—against skeptics like Deaton and Nancy Cartwright, who contend that no method guarantees causality without theory and triangulation, as RCTs can suffer from attrition bias (up to 20-30% in social trials) or Hawthorne effects.[74] [75] Empirical comparisons reveal mixed results: a 2022 analysis of labor interventions found quasi-experimental estimates aligning with RCTs 70-80% of the time when assumptions hold, but diverging in heterogeneous contexts, underscoring that alternatives can match RCT precision while better capturing policy-relevant variation.[76] In impact evaluation, over-reliance on RCTs, often promoted by institutions with vested interests in experimental methods, risks sidelining credible quasi-experimental evidence from natural experiments, as seen in macroeconomic policy assessments where observational designs have informed reforms like conditional cash transfers in Brazil.[77]| Approach | Key Strength | Key Limitation | Example Application |
|---|---|---|---|
| RCTs | High internal validity via randomization | Poor scalability, ethical barriers, limited generalizability | Microfinance impacts in India (2000s trials showing modest effects)[68] |
| Quasi-Experimental (e.g., DiD, RDD) | Leverages real-world data for broader applicability | Depends on assumptions like parallel trends, testable but not always verifiable | Minimum wage effects (DiD in 1994 U.S. study)[72] |
