Violence, Domestic

6

Review clinical trials related to Violence, Domestic. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Community Resiliency Collective Efficacy Intervention

This study will evaluate, via a cluster-randomized controlled trial, the effectiveness of a community-centered intervention that promotes thriving and resiliency to reduce community violence.

Participants needed: 4,600
Trial details
Age: 13+Biological sex: AllType: InterventionalSponsor: University of PittsburghUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

youth age 13 years old and up (all genders) [+2]

individuals younger than 13 years old [+1]

Status: Recruiting

Substance Misuse and Family Violence Treatment Fathers

This study involves a randomized controlled trial of Fathers for Change (F4C) compared to Individual Drug Counseling (IDC) with a sample of 280 fathers enrolled in substance use (SU) treatment within community or veterans (VA) healthcare settings to (a) demonstrate F4C efficacy compared to IDC in reducing SU and family violence (FV) at end of treatment, 3- and 6-month post-treatment follow-up, and (b) document improved emotion regulation as the mechanism within F4C that results in reduced SU and FV.

Participants needed: 280
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Yale UniversityUpdated: May 22, 2026Locations: 2
Eligibility criteria

meet DSM-5 criteria for an SU disorder at the time of assessment at APT or VACHS... [+4]

an active full/no contact protective order pertaining to their child; [+5]

Status: Recruiting

1MoreStep: An Intervention to Increase HIV Care Engagement and Reduce Intimate Partner Violence Among Black Women Living With HIV

This study tests a 5-session cognitive behavioral approach program (herein referred to as the 1MoreStep intervention) to train Black women living with HIV (BWLWHI) and exposed to intimate partner violence (IPV) in the past 2 years (hereafter, BWLWHI) in: 1) cognitive and behavioral skills to access internal and external sources of strength (e.g. self-reliance, safety net); safety strategies, knowledge about Undetectable = Untransmissible (U=U) and HIV care; and reduce internalized and anticipated stigma; 2) communication skills to respond to enacted HIV and IPV stigma and enlist social support; and 3) addressing structural barriers to HIV care engagement with an HIV navigator component. The intervention is informed by the HIV-Stigma Framework and a resilient-reintegration model which views women as active participants in responding to IPV and managing life with HIV. Aim 1: Examine preliminary efficacy of the 1MoreStep intervention on: (a) IPV safety strategies (informal and formal resources, safety planning, and placating strategies at baseline, 3-month and 6-month follow-up visits); and (b) HIV care engagement (medical record confirmed visit with an HIV care provider, antiretroviral therapy (ART) prescription, medication adherence, and viral load status during 3-month and 6-month follow-up visits). Aim 2: Examine the acceptability and feasibility of the 1MoreStep intervention operationalized by (a) quantitative measures: session attendance and fidelity to key intervention components and (b) qualitative interviews to assess: program fit, facilitators and barriers to participation, and using 1MoreStep intervention skills.

Participants needed: 100
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Johns Hopkins UniversityUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

Cis-gender female [+8]

Not a Cis-gender female [+8]

Status: Recruiting

Trauma Screening/Referral and Interpersonal Violence Prevention for Women with Substance Use Disorders

The purpose of this project is to implement a pilot study to investigate the feasibility and preliminary efficacy of a peer support specialist delivered violence prevention program for women in substance use treatment. The program entails a posttraumatic stress disorder (PTSD) screening, resource referral, and two session interpersonal violence prevention protocol for 60 participants. In this single arm trial, women are recruited from three substance use treatment facilities. Participants complete baseline, post-intervention, one-month, and three-month follow-up assessments. Self-report surveys assess trauma exposure, knowledge and behaviors related to interpersonal violence, and intervention engagement.

Participants needed: 60
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Clemson UniversityUpdated: Sep 23, 2024Locations: 2
Eligibility criteria

Not listed

Status: Recruiting

A Couple-based Gender-transformative Intervention on IPV Against Infertile Women

This is a multicenter, open-label, randomized controlled trial conducted at two reproductive medicine centers in Beijing, China. Couples undergoing their first or second in-vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) cycle, diagnosed with female-factor infertility, and who have signed informed consent will be enrolled. Exclusion criteria include couples receiving donated oocytes, sperm, or embryos; those diagnosed with severe male-factor infertility or unexplained infertility; those undergoing preimplantation genetic testing (PGT); those who have not undergone embryo transfer within six months after oocyte retrieval; those with severe mental disorders; and those who withdraw from the study. Participants are will randomly allocated 1:1 by center to either the intervention or control group. Couples in the intervention group will receive five 60-minutes GTI sessions focusing on gender norms, gender equality, and healthy relationship skills, conducted by trained healthcare providers and social workers. The control group will receive standard reproductive care. A total of 376 infertile couples will be enrolled (188 couples per group). The primary outcome is the IPV rate against infertile women over the past 12 months.

Participants needed: 752
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Peking University Third HospitalUpdated: Aug 28, 2024Locations: 2
Eligibility criteria

Couples who are undergoing their first or second IVF/ICSI cycle; [+2]

Couples who receive donated oocytes, sperm, or embryos; [+5]

Status: Recruiting

Healing Circles: An Intervention for Canadian Indigenous Mothers & Children Affected by IPV

Evaluation of Mother's Empowerment Program and Kid's Club Program adapted specifically for Indigenous mothers and children affected by intimate partner violence in Canada

Participants needed: 160
Trial details
Age: 6-13Biological sex: AllType: InterventionalSponsor: University of ManitobaUpdated: Mar 15, 2024Locations: 1
Eligibility criteria

mothers self-reported experience of past intimate partner violence, English-spea...