- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03220412
Viewing Movie Violence & Interest in Guns
May 30, 2019 updated by: Brad Bushman, Ohio State University
Exposure to Gun Violence in Movies Increases Interest in Real Guns
More American children die by accidental gun use than children in other developed countries.
One factor that can influence children's interest in guns is exposure to media containing guns.
The objective of this study is to test whether children who see a movie containing guns will handle a real gun longer and will pull the trigger more times than children who see the same movie without guns.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A recent analysis of top selling films found that the depiction of guns in violent scenes in PG-13 films that target youth has increased from the level of G and PG files in 1985 when the rating was introduced, to the level of R films by 2005, to exceed the level of R films since 2012.
By definition, a PG-13 movie is supposed to have less violence than an R-rated movie.
The Motion Picture Association of America says on its website that the violence in a PG-13 movie "does not reach the restricted R category."
Our study shows that it does.
By including guns in violent scenes, film producers may be inadvertently increasing aggression in youth via a weapons effect.
This experiment directly tests this hypothesis.
Study Type
Interventional
Enrollment (Actual)
104
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
8 years to 12 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
Age 8-12yrs, had not participated in study prior, was able to schedule participation with a known peer (8-12yo).
Exclusion Criteria:
Younger than 8yo, older than 12yo, had participated in study prior, could not schedule participation with a known peer (8-12yo)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Condition
Intervention was guns in movies.
Participants in this condition viewed a movie with guns, as it was filmed and distributed.
The actual scenes in the movie (National Treasure or The Rocketeer) was not edited, but the same scenes were used as the Experimental Condition Intervention is m
|
Participants in this arm viewed movies (National Treasure, The Rocketeer) without guns.
The movies, rated PG, were edited to remove guns from the scenes
|
|
No Intervention: Control Condition
Participants in this condition viewed a movie without guns.
The movie (National Treasure or The Rocketeer) was edited to remove guns from scenes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trigger Pulls
Time Frame: 20 minutes after intervention
|
The adjusted median of the number of trigger pulls per child.
These data refer to the reduced Generalized Estimating Equation model for the two conditions.
This model included participant gender and condition, bu not any of the other control variables.
|
20 minutes after intervention
|
|
Seconds Holding Gun
Time Frame: 20 minutes after intervention
|
Number of seconds participant held gun
|
20 minutes after intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Brad J Bushman, PhD, The Ohio State Universit
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 15, 2015
Primary Completion (Actual)
January 1, 2016
Study Completion (Actual)
January 1, 2016
Study Registration Dates
First Submitted
July 14, 2017
First Submitted That Met QC Criteria
July 17, 2017
First Posted (Actual)
July 18, 2017
Study Record Updates
Last Update Posted (Actual)
June 3, 2019
Last Update Submitted That Met QC Criteria
May 30, 2019
Last Verified
May 1, 2019
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2013B0542-3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
We are considering making individual participant data available, but need to determine steps and appropriateness according to our institutional IRB board.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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