Media Regulation and Viewer Reactions: Editorial constraints and viewers' demand

Last registered on May 21, 2025

Pre-Trial

Trial Information

General Information

Title
Media Regulation and Viewer Reactions: Editorial constraints and viewers' demand
RCT ID
AEARCTR-0016043
Initial registration date
May 20, 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
May 21, 2025, 3:49 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
University of Mannheim

Other Primary Investigator(s)

PI Affiliation
ENS de Lyon

Additional Trial Information

Status
In development
Start date
2025-05-21
End date
2026-12-31
Secondary IDs
Prior work
This trial is based on or builds upon one or more prior RCTs.
Abstract
This study examines whether editorial constraints shaped by broadcast regulation affect audience demand for television talk shows.
External Link(s)

Registration Citation

Citation
Mougin, Elisa and Camille Urvoy. 2025. "Media Regulation and Viewer Reactions: Editorial constraints and viewers' demand." AEA RCT Registry. May 21. https://doi.org/10.1257/rct.16043-1.0
Sponsors & Partners

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Experimental Details

Interventions

Intervention(s)
* Randomized information treatment
Intervention Start Date
2025-05-21
Intervention End Date
2025-06-06

Primary Outcomes

Primary Outcomes (end points)
* Willingness to watch the new show (scale from not at all to yes, certainly)
* Expected features of the new show (entertaining, factually accurate, different from other talk shows, etc.) (scales from no, not at all to yes, a lot).
Primary Outcomes (explanation)
See pre-analysis plan

Secondary Outcomes

Secondary Outcomes (end points)
* Open ended question regarding what comes to mind when thinking about the new show compared to the previous one.
* Whether they anticipate the host to comply with those rules.
Secondary Outcomes (explanation)
See pre-analysis plan

Experimental Design

Experimental Design
See attached plan (registered before the trial, will be published when the trial is complete).
Experimental Design Details
Not available
Randomization Method
Randomization done in office by a computer
Randomization Unit
Individual level
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
As many clusters as individuals. See below for the number of individuals.
Sample size: planned number of observations
4,159 participants will be contacted. We expect that around 3,000 of them will complete the survey. The sample of 4,159 contacted participants consists in the individuals who took the first wave of our survey. This earlier data collect effort was described in AEARCTR-0015302.
Sample size (or number of clusters) by treatment arms
We plan to randomly split out sample into three groups of equal size. We expect around 1,000 respondents per group.
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
IRB

Institutional Review Boards (IRBs)

IRB Name
Ethics Committee University of Mannheim
IRB Approval Date
2025-01-31
IRB Approval Number
EC Mannheim 3/2025
Analysis Plan

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