State-card readability under tricolor priming: an equivalence test

Last registered on June 15, 2026

Pre-Trial

Trial Information

General Information

Title
State-card readability under tricolor priming: an equivalence test
RCT ID
AEARCTR-0018838
Initial registration date
June 05, 2026

Initial registration date is when the trial was registered.

It corresponds to when the registration was submitted to the Registry to be reviewed for publication.

First published
June 15, 2026, 1:36 PM EDT

First published corresponds to when the trial was first made public on the Registry after being reviewed.

Locations

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Primary Investigator

Affiliation
CIDE

Other Primary Investigator(s)

Additional Trial Information

Status
In development
Start date
2026-05-06
End date
2026-10-31
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
We test whether the inclusion of the Mexican flag tricolor (red/white/green) in a visual card depicting a beneficiary state affects participants' subsequent memory of which state the card depicted. The intervention is a 10-second exposure to one of 12 cards (6 Mexican states x 2 versions: tricolor styling vs. teal styling, applied to the card border and to the donor-state name) presented within a brief in-person survey administered on participants' own devices. The hypothesis under test is one of **equivalence**: flag exposure does not impair state retention relative to neutral exposure within a margin of plus-or-minus 10 percentage points. The primary outcome is whether the participant correctly identifies the donor state by either open-ended recall or multiple-choice recognition. The study responds to a referee concern on a manuscript that draws from an earlier study (AEARCTR-0005236). The sample is 200 participants (100 per arm) recruited from undergraduate populations at four Mexico City universities (CIDE, ITAM, Ibero, possibly Anahuac del Sur). Primary inference is by two one-sided test (TOST) for equivalence on the flag-minus-neutral difference of proportions, requiring the Newcombe 90% confidence interval to fall entirely within the plus-or-minus 10 pp band. A small calibration pilot (N approximately 30, May 2026) informed the power calculation; pilot data are not included in the registered analysis.
External Link(s)

Registration Citation

Citation
Fernandez Duque, Mauricio. 2026. "State-card readability under tricolor priming: an equivalence test." AEA RCT Registry. June 15. https://doi.org/10.1257/rct.18838-1.0
Experimental Details

Interventions

Intervention(s)
Participants take a brief (approximately 5-minute) survey administered via oTree on their own devices, in person, in a classroom setting at one of four Mexico City universities (CIDE, ITAM, Ibero, possibly Anahuac del Sur).
Intervention Start Date
2026-05-06
Intervention End Date
2026-10-31

Primary Outcomes

Primary Outcomes (end points)
`state_memory_either` -- a binary indicator equal to 1 if the participant correctly identifies the donor state via either open-ended recall (Screen 6) or 6-alternative forced choice recognition (Screen 7), and 0 otherwise.

Primary Outcomes (explanation)
The OR-rule reflects the substantive question of interest: whether the participant has retained the donor-state identity from the exposure. A participant who recognizes the state from a list but cannot freely recall it has, in substance, retained the state's identity. Restricting the outcome to recall-only would treat such a participant as a memory failure, mismatching the substantive question. Free recall and recognition are reported as components alongside the primary for transparency.

Secondary Outcomes

Secondary Outcomes (end points)
Primary outcome components (reported alongside the primary)

- `recall_state_correct` -- open-ended free recall of the donor state (Screen 6), scored with a fuzzy canonical-name match (Levenshtein-tolerant against the canonical Spanish state name).
- `state_recognition_correct` -- 6-alternative forced choice recognition of the donor state from a fixed list of six Mexican states with per-participant shuffle (Screen 7).


Additional measured outcomes

The below outcome is part of the instrument by design. It is reported descriptively -- per-arm rates and a companion two-proportion test -- for transparency about the data collected. It is not pre-committed gates on H1: the verdict on the readability confound is not conditioned on any of these outcomes.

- `org_recall_correct` -- open-ended free recall of the donor organization shown on the card (Screen 5). Also serves as the buffer task between the card exposure and the state-recall question.
Secondary Outcomes (explanation)
Regarding the primary outcome components: Both components are reported with the same TOST equivalence test as the primary (plus-or-minus 10 pp margin, Newcombe 90% CI, alpha = 0.05 per tail), plus companion NHST, so a reader can see how equivalence behaves on each component as well as on the OR combination.

Experimental Design

Experimental Design
Two-arm between-subject randomized controlled trial. Individual-level random assignment. No clustering. Fixed-N, no peeking.
Experimental Design Details
Not available
Randomization Method
At-individual level, deterministic per participant from the anonymous participation code: the code is hashed to a 64-bit integer and used to seed the choice of arm, the choice of beneficiary state from the 6-state pool, the bonus-question draw, and the per-participant shuffle of the 6-alternative forced choice recognition options. Reproducibility from the saved code is exact.
Randomization Unit
University affiliates (students and staff)
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
Not applicable
Sample size: planned number of observations
200 university affiliates (students and staff) total. Fixed-N, no peeking.
Sample size (or number of clusters) by treatment arms
100 per arm
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
At the planned N (100 per arm), Monte Carlo TOST power on the OR primary is 80.3% (B = 20,000 simulation replications; 95% Monte Carlo CI [80.0%, 80.9%]), at alpha = 0.05 per tail, equivalence margin plus-or-minus 10 pp, anchored at p_neutral = 0.97 and p_flag = 0.95. The anchor reflects an expectation of high recall under the stimulus design: the cards are clear single-state illustrations shown for 10 seconds, intentionally well above the threshold at which differential reading speed would be the bottleneck. A small calibration pilot (N approximately 30, May 2026, CIDE undergraduate convenience sample) validated this anchor empirically and confirmed instrument functioning (exposure time tight at 10.15-10.43 s; zero bonus-computation mismatches; clean arm x state and arm x bonus-question balance). Pilot data are not included in the registered analysis and the pilot was conducted on a separate population from the main wave. Power was computed by direct Monte Carlo simulation of the TOST procedure on the OR primary, not by closed-form normal approximations. At the empirical-ceiling anchor (0.97 / 0.95), the power function is discrete-stepped in (k_flag, k_neutral) against the integer thresholds of the Newcombe-CI band edges, making asymptotic normal approximations unreliable. The exact simulation code, anchor sweeps, and per-N power values are in `analysis/power_sweep.R` and `analysis/power_fine.R`. MDES (minimum detectable effect size) -- reported under both interpretations, since the TOST design admits two: 1. As equivalence margin. Delta = 10 pp. This is the smallest true |p_flag - p_neutral| that the test is set up to exclude. Effects below this threshold are declared equivalent. 2. As conventional power-bounded MDES on the companion NHST. Under a standard two-sided two-proportion test at alpha = 0.05 with 80% power at p_neutral = 0.97, the smallest detectable absolute difference at N = 100/arm is approximately plus-or-minus 13 pp. This is the MDES for the companion NHST, not for the primary inference.
Supporting Documents and Materials

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IRB

Institutional Review Boards (IRBs)

IRB Name
Comité de Ética en Investigación del CIDE
IRB Approval Date
2026-06-02
IRB Approval Number
CEI/0005/2026
Analysis Plan

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