N/A
N=119
Violence Prevention for Middle School Boys
Intimate Partner Violence
Bottom Line
View on ClinicalTrials.gov: NCT03109184 ↗Enrolled (actual)
119
Serious AEs
0.0%
Results posted
Nov 2019
Primary outcome: Primary: Change in Dating Violence (DV) Perpetration From Baseline to 9 Months — 46; 40; 14; 14 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Project STRONG (Behavioral)
- Age
- Pediatric · 12+ yrs
- Sex
- Male
- Sponsor
- Northeastern University
- Primary completion
- Aug 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Dating Violence (DV) Perpetration From Baseline to 9 Months |
46; 40; 14; 14; 50; 43 | — |
| PRIMARY Change in General Aggressive Behavior From Baseline to 9 Months |
2.02; 2.01; 2.09; 2.02; 2.03; 1.99 | — |
| PRIMARY Change in Attitudes About Relationship Violence From Baseline to 9 Months |
3.01; 2.98; 3.03; 3.00; 3.10; 3.02 | — |
| SECONDARY Change in Emotion Regulation Skills From Baseline to 9 Months |
3.60; 3.63; 3.55; 3.63; 3.44; 3.71 | — |
| SECONDARY Change in Parent-Adolescent Communication From Baseline to 9 Months |
38.65; 37.65; 36.65; 36.87; 35.13; 35.16 | — |
| SECONDARY Change in Emotion Regulation Skills Baseline to 9 Months |
2.04; 2.18; 2.01; 2.18; 1.86; 2.21 | — |
| SECONDARY Change in Distress Tolerance From Baseline to 9 Months |
256.68; 251.19; 240.98; 230.66; 227.17; 243.14 | — |
Summary
This study will develop and test a web-based intervention to enhance emotion regulation skills and parent-son relationship communication to decrease adolescent boys' risk for dating violence involvement as well as attitudes supporting relationship aggression.
Eligibility Criteria
Inclusion Criteria
- 1) adolescent enrolled in the 7th or 8th grade,
- 2) parent/legal guardian and teen are English speaking,
- 3) parent/legal guardian is willing to provide consent for the adolescent to participate in the study,
- 4) adolescent is willing to provide assent for their own participation.
Exclusion Criteria
- 1) observable cognitive or developmental delays that would preclude participation,
- 2) residing with participating parent/guardian less than half time
Data sourced from ClinicalTrials.gov (NCT03109184). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.