Rule Following and Cooperation - An Information Provision Experiment

Last registered on July 28, 2025

Pre-Trial

Trial Information

General Information

Title
Rule Following and Cooperation - An Information Provision Experiment
RCT ID
AEARCTR-0016445
Initial registration date
July 24, 2025

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
July 28, 2025, 9:19 AM 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
University of Nottingham

Other Primary Investigator(s)

PI Affiliation
University of Nottingham
PI Affiliation
University of Nottingham

Additional Trial Information

Status
In development
Start date
2025-07-29
End date
2026-09-30
Secondary IDs
Prior work
This trial is based on or builds upon one or more prior RCTs.
Abstract
Social expectations are a key element of the CRISP (Gaechter, Molleman and Nosenzo, 2025) framework in explaining rule conformity and cooperation. In this set of experiments we consider how shifting expectations, by providing information about the behaviour of previous subjects, influences behaviour. A core component of the CRISP framework is that social expectations influence rule conformity and cooperation to the extent individuals condition their behaviour on their beliefs about what others do. Employing the ABC approach (Gaechter, Koelle and Quercia, 2017) we aim to demonstrate that the effectiveness of shifting beliefs depends on the degree of conditionality of subjects preferences, with conditional types responding the most to our belief manipulations.
External Link(s)

Registration Citation

Citation
Cubitt, Robin, Simon Gaechter and Pierce Gately. 2025. "Rule Following and Cooperation - An Information Provision Experiment." AEA RCT Registry. July 28. https://doi.org/10.1257/rct.16445-1.0
Experimental Details

Interventions

Intervention(s)
Intervention Start Date
2025-07-29
Intervention End Date
2025-08-19

Primary Outcomes

Primary Outcomes (end points)
The number of tokens placed in the blue bucket is the primary outcome of interest as it indicates the level of subjects’ rule following and cooperative behaviour, respectively. Within the CRISP paradigm this is our measure of Conformity/Cooperation. We elicit subjects’
conditional allocations to the blue bucket via the strategy method to capture their Conditional Preferences and follow the protocol of Thoni and Volk (2018) in classifying subjects’ propensity to cooperate (i.e., their attitudes in the ABC approach). We elicit subjects Normative and Descriptive Beliefs (jointly their Social Expectations) and their personal norms (capturing Respect for Rules).
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
The study is divided into two parts. Part two will take place at least one week after Part one. Part one replicates the design of AEARCTR-0014964 with minor modifications. Namely, we elicit subjects cognitive uncertainty about their normative and descriptive beliefs, following the approach of Enke and Graeber (2023). We also amend the way in which we elicit subjects descriptive beliefs in stage four of the experiment, and subjects only complete one strategy method experiment in which they can condition their own behaviour on the average behaviour of other subjects. Part two takes place at least one week later and invites subjects from Part one to take part.
Experimental Design Details
Not available
Randomization Method
Subjects will be randomly allocated into treatments by the LIONESS Lab software (Giamattei et al., 2020). In Part one we randomise subjects until each task has reached the desired sample size of 264. Once a task has achieved a sample size of 264 future subjects will no longer be randomised to that task. In Part two we randomise subjects until each treatment within a task (i.e., high signal Baseline RFT, low signal Baseline RFT, high signal Baseline PGG, low signal Baseline PGG) has reached the desired sample size of 132. Once a treatment has achieved a sample size of 132 future subjects will no longer be randomised to that task.
Randomization Unit
In Part one subjects are randomly allocated to one task. In Part two they are randomly allocated to one treatment within the same task they completed in Part one. The order in which we elicit subjects descriptive and normative beliefs is also randomised.
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
As each subject makes multiple decisions, we will cluster at the level of the individual.
Sample size: planned number of observations
In part one of the study we will collect 528 subjects in total.
Sample size (or number of clusters) by treatment arms
In part one of the study we will collect 528 subjects in total, 264 per treatment (i.e., 264 in Baseline RFT, and 264 in Baseline PGG). Based on pilot data our treatment manipulation had an effect size of approximately 0.88 (comparing the difference in mean beliefs between the high and low signal with a Mann-Whitney test). Power calculations indicate we require a sample size of 224 subjects per task (ensuring n is divisible by group size of 4) to detect such an effect (alpha=.001, beta=0.999). In the pilot 88% of subjects who completed Part one subsequently completed Part two. Assuming the same retention rate, we plan to recruit 264 subjects per task for a total sample size of 264*2 = 528 subjects.

Part two will take place one week later on the Prolific platform and will invite all 528 subjects back. Subjects within each treatment arm will be randomised to either see a high or low signal about the average number of tokens previous groups placed in the blue bucket. Of the 264 subjects in each treatment 132 will see the high signal and 132 will see the low signal (i.e., 132 in Baseline RFT high signal, 132 in Baseline RFT low signal, 132 in Baseline PGG high signal, and 132 in Baseline PGG low signal).

Part two will remain active on the Prolific platform for two weeks. Depending on the number of subjects who return to complete part two we will recruit additional new subjects to ensure that the final subject size in part two is divisible by the required group size.

Exclusion Criteria: We will exclude any incomplete data, and consider the first 264 complete submissions in each task from subjects who submitted a completion code on Prolific. Subjects’ who answer comprehension questions incorrectly 2 or more times in Baseline RFT (3 or more times in Baseline PGG) are screened out of the study. In our analysis we will exclude: (i) subjects’ who self-report that they did not pay attention during the study* (ii) subjects in Baseline PGG who completed the study in 10 minutes or less (iii) subjects in Baseline RFT who completed the study in 8 minutes or less (iv) subjects who report they did not understand the decision scenario**. After applying these exclusion criteria if the sample size in any task drops below 264 we will recruit additional subjects to make up the difference in the impacted task (e.g., if the sample drops to 263 in Baseline RFT, we will recruit 1 additional subject fulfilling the aforementioned non-exclusion criteria to the Baseline RFT task). *This is based on subjects’ response to the following question: “The following question does not affect your payment, and is only used for data quality purposes. Please indicate the extent to which you agree with the statement: Throughout the study I was paying sufficient attention.” with response options Strongly Disagree, Disagree, Agree, Strongly Agree. We will exclude those who do not indicate Agree or Strongly Agree. **This is based on subjects’ response to the following question: “Please indicate how certain you are that you understand how this interaction works and how your bonus payment is calculated. 0% means ‘completely uncertain’ and 100% means 'completely certain’.” With response options 0/10/20/30/40/50/60/70/80/90/100%. We will exclude those who indicate 50% or lower.
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
Based on pilot data our treatment manipulation had an effect size of approximately 0.88 (comparing the difference in mean beliefs between the high and low signal with a Mann-Whitney test). Power calculations indicate we require a sample size of 224 subjects per task (ensuring n is divisible by group size of 4) to detect such an effect (alpha=.001, beta=0.999). In the pilot 88% of subjects who completed Part one subsequently completed Part two. Assuming the same retention rate, we plan to recruit 264 subjects per task for a total sample size of 264*2 = 528 subjects.
IRB

Institutional Review Boards (IRBs)

IRB Name
The Nottingham School of Economics Research Ethics Committee
IRB Approval Date
2025-05-19
IRB Approval Number
ERCP-2024-043-rulefollow-coop6
Analysis Plan

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