Methods & Evaluation Design (jppm-methods)
When to trigger
- Deciding whether the question needs an experiment, a policy evaluation, a survey, or a synthesis
- A policy rolled out and you must find a credible counterfactual before claiming impact
- Your label/disclosure experiment uses stimuli no agency could ever mandate
- The sample excludes the very population the policy is meant to protect
- You are combining lab and field evidence and need the pieces to carry distinct weight
Methodological pluralism, disciplined by the policy question
JPP&M accepts a wider methods palette than most marketing journals — randomized experiments, quasi-experimental evaluation, surveys, field and archival data, meta-analysis, qualitative work — but the choice must follow from the policy inference required. Two questions dominate: Would the proposed instrument work? (prospective — usually experiments with realistic stimuli) and Did the enacted instrument work? (retrospective — evaluation designs with explicit counterfactuals). A submission that answers the retrospective question with before/after trends, or the prospective one with fantasy stimuli, fails regardless of statistical polish. Missing counterfactual reasoning in an evaluation design is one of this journal's known desk-reject patterns.
Prospective designs: policy-realistic experiments
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Mandatable stimuli. Test warning/label/disclosure formats an agency could actually require — real estate on a package, formats from the live rulemaking (e.g., FDA front-of-package proposals), not a full-screen banner no rule would compel.
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Treatment contrasts = decision options. Conditions should map to the regulator's choice set (status quo vs. proposed rule vs. stricter alternative), so each pairwise contrast answers a decision.
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Consequential outcomes. Choice with real stakes, purchases, incentivized behavior — self-reported intentions alone are weak currency for a claim that a rule will change behavior.
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Policy-relevant samples. Recruit the protected population (smokers for tobacco warnings, low-income households for financial disclosures, parents for children's marketing). A student panel cannot carry a vulnerability claim; when using Prolific/CloudResearch, screen and quota accordingly.
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Marketplace noise. Add realistic competing information (cluttered shelf, competing claims); effects that survive noise are the ones that survive markets.
Retrospective designs: evaluation with a counterfactual
| Design |
Use when |
JPP&M-specific cautions |
| Difference-in-differences |
policy adopted in some states/markets/categories, not others |
staggered adoption needs heterogeneity-robust estimators; argue parallel trends behaviorally, not just visually |
| Regression discontinuity |
eligibility threshold or size cutoff assigns exposure |
check manipulation at the cutoff (firms sort!); effects are local to the threshold |
| Synthetic control |
one large unit treated (a city soda tax, a national ban) |
pre-period fit and placebo runs are the argument |
| Event study |
timing of enforcement/announcement is sharp |
anticipation by firms and media coverage blur the event date |
| Interrupted time series |
no untreated comparison exists at all |
weakest option; state so and bound the claims |
Firms' strategic responses are both a threat and a finding: reformulation, pre-emptive compliance, or channel-shifting can contaminate the comparison group — design to detect it (untreated outcomes, supply-side data) rather than assume it away.
Surveys, qualitative work, and synthesis
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Surveys earn their place for constructs no archive holds (perceived deception, privacy concern, financial anxiety) — use validated scales and probability or well-quota'd samples when claims are population-level.
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Qualitative designs are welcome for vulnerable populations whose experience frames the policy problem; document access, consent, and IRB care to a higher standard, and avoid designs that further burden participants.
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Meta-analysis suits mature streams (warning-label effects, disclosure formats); code moderators the regulator controls (format, placement, dose).
Checklist
Anti-patterns
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Before/after theater: a pre/post trend presented as policy impact with no comparison group
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Fantasy stimuli: disclosure formats no agency could mandate, generalized to regulation
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Convenience-sample vulnerability claims: conclusions about protected groups from panels that exclude them
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Intentions-only evidence for behavior-change claims
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One-method dogma: forcing an experiment onto a question that demands field variation, or vice versa
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Sorted cutoffs: an RDD where firms demonstrably manipulate the threshold, unexamined
Output format
【Policy question type】prospective (would it work) / retrospective (did it work)
【Design】experiment / DiD / RDD / synthetic control / survey / meta-analysis / qualitative
【Counterfactual】comparison group + assignment logic (retrospective) or control condition logic (prospective)
【Stimuli & sample】mandatable formats; policy-target population included
【Firm response plan】how strategic reactions are detected or bounded
【Next skill】jppm-data-analysis