- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07494617
Behavior and Risk Awareness Through Video Education for Firefighters (BRAVE)
BRAVE: Behavior and Risk Awareness Through Video Education for Firefighters
The goal of this clinical trial is to evaluate the impact of short documentary-style videos to educate and inspire firefighters to take safety measures to prevent cancer incidence and mortality.
The main question it aims to answer is:
Will firefighters will have a higher perceived susceptibility to cancer, lower perceived barriers to cancer risk reduction practices, and higher perceived self-efficacy and benefit to risk reduction practices after watching the videos?
Participants will:
- Take a Pre-Intervention survey
- Watch one of five randomly assigned 5 minute video interventions
- Take a Post-Intervention survey
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Shehnaz K Hussain, PhD
- Phone Number: 310-429-9859
- Email: skhussain@health.ucdavis.edu
Study Contact Backup
- Name: Tony Nguyen, BS
- Phone Number: 9162161169
- Email: ttnguye@health.ucdavis.edu
Study Locations
-
-
California
-
Sacramento, California, United States, 95817
- Recruiting
- UC Davis Health
-
Contact:
- Tony T Nguyen
- Phone Number: 916-734-4534
- Email: ttnguye@health.ucdavis.edu
-
Principal Investigator:
- Shehnaz K Hussain, PhD
-
Sub-Investigator:
- Derek Urwin, PhD
-
Sub-Investigator:
- Laura Fejerman, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Current active career California firefighter
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Video 1
Participants assigned to video 1
|
San Francisco, brain cancer survivor
|
|
Experimental: Video 2
Participants assigned to video 2
|
Sacramento, colorectal/lung cancer
|
|
Experimental: Video 3
Participants assigned to video 3
|
LA, colorectal cancer
|
|
Experimental: Video 4
Participants assigned to video 4
|
LA, melanoma
|
|
Experimental: Video 5
Participants assigned to video 5
|
LA, breast cancer
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Post-Intervention Survey
Time Frame: Analyses will take place within 12 months of study initiation.
|
Questions within the domains of the health belief model (HBM) including perceived susceptibility, perceived barriers to actions, self-efficacy, perceived benefits, perceived severity, and cue to action.
|
Analyses will take place within 12 months of study initiation.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2265741
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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