- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07404800
Longitudinal Investigation of the Risk and Protective Factors of Dating Violence (Dating it Safe) - Firearms
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Texas
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Houston, Texas, United States, 77054
- The University of Texas Health Science Center at Houston
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Waves 1-13 (years 2010-2024): High school freshman and sophomores located at a designated study school and classroom that returned a signed parent consent form and student assent form.
- Beginning with Wave 10, current partners of participants are eligible to participate.
- Waves 13 - 14 (years 2024-2025) + Firearm injury and violence (FIV) cohort: Original study participants from Waves 1-13 and their current partners will be asked gun usage survey questions. Anyone endorsing gun carriage in Wave 11 will be eligible for an in-depth interview in Waves 13 - 14.
Exclusion Criteria:
- Anyone not originally consented in 2010 or not a current partner of a participant originally consented in 2010 is not eligible to participate in the research survey. Participants who declined to participate or passed away during previous waves will not be included. Anyone not endorsing gun carriage in Wave 11 will be excluded from in-depth interview invitations.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Cohort consists of adult participants with an average age of 28 - 30 years old.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Identify key individual (e.g., demographic, socioeconomic, attitudes), relationship, behavioral and situational, trauma related, and neighborhood/community risk and protective factors for gun access, carriage, and use.
Time Frame: From 2024 to 2027
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From 2024 to 2027
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Qualitative interviews with known gun-carriers
Time Frame: 2024-2027
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Conduct a series of 60 in-depth semi-structured interviews with known gun-carriers (Mean age = 26) recruited from Wave 10 of the ongoing study to better understand their thinking, practices, contexts, and experiences of acquiring, carrying, using, sharing, and storing firearms.
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2024-2027
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Disseminate evidence based products
Time Frame: 2024-2027
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Taking the complex political environment into account, we will translate results into jargon-free language and disseminate evidence-based products (i.e., policy briefs, summary reports) to policymakers and practitioners to inform FIV prevention legislation. By leveraging and extending the scope and breadth of our robust longitudinal dataset and conducting in-depth qualitative interviews of known gun carriers, we will enhance our understanding of the risk and protective factors related to firearm access, carriage, and use. Findings from this mixed-methods project will directly benefit the field by informing policy and the evolution of developmentally appropriate evidence-based interventions, with the ultimate goal of reducing firearm violence among adolescents and young adults. |
2024-2027
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Jeffrey R Temple, PhD, The University of Texas Health Science Center, Houston
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
- HSC-MS-24-0006
- R01CE003614 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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