- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07548437
Rise up! A Youth-Informed Video Program For Young Children To Stay Safe From Community Violence
April 24, 2026 updated by: The University of Texas Medical Branch, Galveston
Rise Up! A Youth-Informed Video Program To Prevent Community Violence Before The First Shot
Gun violence is the number one reason children die in the U.S. In big cities, most of these cases come from shootings related to assaults and homicides.
There aren't many effective ways right now to prevent kids from either becoming victims or getting involved in gun violence themselves.
This study aims to create a video program (Rise Up! Against Violence) for middle schoolers that teaches them about guns and the real-life consequences of violence.
The videos will be made by high school students who have personally experienced gun violence, since they may be better able to connect with and influence younger kids.
The Rise Up! program will be tested in schools in high-violence communities in Houston and Memphis.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Detailed Description
Community gun violence is the leading cause of firearm injury and death in urban youth in the United States and yet upstream primary prevention efforts are sparse.
The goal of this proposal is to develop and test a novel youth-informed video-based program to effectively influence young adolescents to avoid risky behaviors leading to gun violence.
Through an innovative iterative process by first seeking the perspective of youth with lived experience with gun violence regarding salient topics and messaging.
Next, by garnering the valuable input and guidance of experienced community-based violence interrupters and a multidisciplinary team of other violence content experts to create a series of videos that will resonate with young adolescents.
The videos will include awareness about consequences of gun use, peaceful conflict resolution skills, hope for the future, and gaining adult support, in addition to other topics.
The investigators will seek community feedback to ensure relatability and cultural humility.
The video series will be delivered as a program ("Rise Up Against Gun Violence") including guided discussions, and will be implemented and rigorously tested in diverse community settings in high-risk neighborhoods in Houston and Memphis.
The investigators hypothesize that the program, developed using a holistic and community-based approach, will influence adolescent attitudes, awareness, and behavior change regarding violent conflict and gun carrying, and ultimately change social norms regarding risks of gun use.
This is an upstream and novel prevention strategy for community gun violence.
Study Type
Interventional
Enrollment (Estimated)
600
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Texas
-
Galveston, Texas, United States, 77555
- The University of Texas Medical Branch
-
-
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
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Children between 11 and 15 years of age
- Residing in one of the six identified high-risk communities, with or without prior exposure to gun violence
Exclusion Criteria:
- Not fluent in English or Spanish
- Under the guardianship of Child Protective Services (CPS)
- Documented suicidal ideation at the time of screening
- Not mentally capable of providing informed assent
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: Prevention
- Allocation: N/A
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group receiving intervention
All subjects will receive the intervention (Rise Up! video program), cluster randomized between the 6 sites.
|
Watch series of videos followed by guided discussion after each video.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Attitude change about the consequences of gun carrying and fighting
Time Frame: 9 months
|
Participants will complete validated pre- and post-intervention surveys adapted from the Youth Risk Behavior Survey, Attitudes Toward Violence Survey, Teen Conflict Survey, and Individual Protective Factors Index.
Survey items use Likert-type and frequency-based response scales to assess changes in knowledge, attitudes, conflict resolution behaviors, and protective factors related to violence prevention.
Higher scores indicate improved protective factors and more positive conflict resolution attitudes.
|
9 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Bindi Naik-Mathuria, MD, MPH, The University of Texas Medical Branch, Galveston
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 (Estimated)
July 1, 2026
Primary Completion (Estimated)
June 1, 2028
Study Completion (Estimated)
September 1, 2028
Study Registration Dates
First Submitted
April 16, 2026
First Submitted That Met QC Criteria
April 16, 2026
First Posted (Actual)
April 23, 2026
Study Record Updates
Last Update Posted (Actual)
April 30, 2026
Last Update Submitted That Met QC Criteria
April 24, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 25-0286
- 1R01CE003772-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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