[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"violence-domestic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:violence-domestic":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,48,80,111,142,164],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100498281","community-resiliency-collective-efficacy-intervention-100498281",false,"NCT05768217","Community Resiliency Collective Efficacy Intervention","Community Resiliency Collective Efficacy Intervention (CRCEI) for Prevention of Community Violence - A Cluster Randomized Controlled Trial","Inclusion Criteria:\n\n* youth age 13 years old and up (all genders)\n* adults 18 years and older (all genders)\n* reside in neighborhoods selected to participate in the study\n\nExclusion Criteria:\n\n* individuals younger than 13 years old\n\n  * individuals residing outside of participating neighborhoods",true,"ALL","13 Years",{"count":20,"type":21},4600,"ESTIMATED","INTERVENTIONAL",[24],"NA","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.",[27,28,29,30,31,32,33,34],"Violence, Physical","Violence, Non-accidental","Violence, Sexual","Violence, Domestic","Violence, Structural","Violence in Adolescence","Community Violence","Social Cohesion","RECRUITING","2026-06-02",{"date":38,"type":39},"2026-06-04","ACTUAL",{"date":41,"type":39},"2024-06-24",{"date":43,"type":21},"2027-09-30",{"name":45,"class":46},"University of Pittsburgh","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":55,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":79},"100566060","phase-2-substance-misuse-and-family-violence-treatment-fathers-100566060","NCT06650267","Substance Misuse and Family Violence Treatment Fathers","Substance Misuse and Family Violence Treatment for Fathers","Inclusion Criteria:\n\n* meet DSM-5 criteria for an SU disorder at the time of assessment at APT or VACHS;\n* report FV within the last 18 months prior to screening (based on self, court, police or child protection reports);\n* have at least one biological child aged 1 to 12 years with whom they live or have at least twice per month in person visits;\n* are able to complete assessments in English; and\n* agree to have their female coparents (mother of the youngest child) contacted for participation of their youngest child. If a participant has more than one child in the age range, the youngest will be the target of assessment and treatment.\n\nExclusion Criteria:\n\n* an active full\u002Fno contact protective order pertaining to their child;\n* physiological addiction to a substance that requires detoxification (such individuals may be re-evaluated following detox);\n* cognitive impairment (a mini mental state score \\\u003C25);\n* current untreated psychotic\u002Fbipolar disorder;\n* currently suicidal or homicidal based on Brief Symptom Inventory Screening and follow-up on positive responses; or\n* are currently receiving weekly individual therapy for Substance misuse or family violence","MALE","18 Years",{"count":58,"type":21},280,[60],"PHASE2","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.",[63,30,64],"Substance Misuse","Child Abuse",[66,67,68,69],"substance misuse","intimate partner violence","domestic violence","treatment","2026-05-21",{"date":72,"type":39},"2026-05-22",{"date":74,"type":39},"2025-02-17",{"date":76,"type":21},"2030-12-31",{"name":78,"class":46},"Yale University",2,{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":87,"minAge":56,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":91,"conditions":92,"keywords":97,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":47},"100486003","1morestep-an-intervention-to-increase-hiv-care-engagement-and-reduce-intimate-partner-violence-among-black-women-living-with-hiv-100486003","NCT05608421","1MoreStep: An Intervention to Increase HIV Care Engagement and Reduce Intimate Partner Violence Among Black Women Living With HIV","1MoreStep: Pilot Trial of an Intervention to Increase HIV Care Engagement and Reduce Intimate Partner Violence Among Black Women Living With HIV","Inclusion Criteria:\n\n* Cis-gender female\n* Black or African American\n* ≥ Age 18\n* Living with HIV\n* ≤ 1 HIV care visit in previous 12 months OR virally unsuppressed (\\>50 copies\u002FmL) OR at high risk for poor HIV care adherence (PHQ ≥ 3, Generalized Anxiety Disorder (GAD) ≥ 3, active substance use)\n* IPV within the previous 2 years\n* Ability to attend in-person for up to 8 sessions\n* Do not report immediate severe danger from their partner\n* English fluency\n\nExclusion Criteria:\n\n* Not a Cis-gender female\n* Not Black or African American\n* ≤ Age17 or younger\n* Not living with HIV\n* ≥ 2 HIV care visits in previous 12 months\n* No IPV within the previous 2 years\n* Inability to attend in-person for up to 8 sessions\n* Reports immediate severe danger from their partner\n* Not fluent in English","FEMALE",{"count":89,"type":21},100,[24],"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.\n\nAim 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).\n\nAim 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.",[30,93,94,95,96],"HIV","Stigma, Social","Engagement, Patient","Medication Adherence",[93,98,99,100,101],"Intimate Partner Violence (IPV)","Black women","Cognitive behavioral approach","Randomized Control Trial (RCT)","2026-04-23",{"date":104,"type":39},"2026-04-29",{"date":106,"type":39},"2023-06-26",{"date":108,"type":21},"2026-12",{"name":110,"class":46},"Johns Hopkins University",{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":16,"sex":87,"minAge":56,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":22,"phases":119,"briefSummary":120,"conditions":121,"keywords":126,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":136,"completionDateStruct":138,"leadSponsor":140,"locationsCount":79},"100562885","trauma-screeningreferral-and-interpersonal-violence-prevention-for-women-with-substance-use-disorders-100562885","NCT06608979","Trauma Screening\u002FReferral and Interpersonal Violence Prevention for Women with Substance Use Disorders","Inclusion Criteria:\n\n1\\) Age 18 or higher;2) female gender identity; 3) currently engaged in substance use treatment or care (behavioral, peer support, pharmacological, medical)\n\n\\-\n\nExclusion Criteria:\n\n1\\) Non-English-speaking; 2) acute physical and medical conditions that interfere with participation in educational sessions (e.g., active psychosis, suicidality).\n\n\\-",{"count":118,"type":21},60,[24],"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.",[122,123,124,29,125,30],"Substance Use Disorders","Posttraumatic Stress Disorder","Opioid Use Disorder","Violence, Gender-Based",[127,128,129,130,131,67,132],"prevention","peer support specialist","substance use disorders","posttraumatic stress disorder","interpersonal violence","sexual violence","2024-09-20",{"date":135,"type":39},"2024-09-23",{"date":137,"type":39},"2024-06-11",{"date":139,"type":21},"2025-03",{"name":141,"class":46},"Clemson University",{"id":143,"slug":144,"hasResults":11,"nctId":145,"briefTitle":146,"officialTitle":147,"acronym":4,"eligibilityCriteria":148,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":149,"targetDuration":4,"studyType":22,"phases":151,"briefSummary":152,"conditions":153,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":79},"100525685","a-couple-based-gender-transformative-intervention-on-ipv-against-infertile-women-100525685","NCT06124950","A Couple-based Gender-transformative Intervention on IPV Against Infertile Women","A Couple-based Gender-transformative Intervention on Intimate Partner Violence Against Infertile Women","Inclusion Criteria:\n\n* Couples who are undergoing their first or second IVF\u002FICSI cycle;\n* Couples diagnosed with female-factor infertility;\n* Couples who have signed consent.\n\nExclusion Criteria:\n\n* Couples who receive donated oocytes, sperm, or embryos;\n* Couples diagnosed with severe male-factor infertility or unexplained infertility.\n* Couples who are undergoing Preimplantation Genetic Testing (PGT);\n* Couples who have not undergone embryo transfer within six months after oocyte retrieval;\n* Couples who have severe mental disorders;\n* Couples who withdrew from the study.",{"count":150,"type":21},752,[24],"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.\n\nParticipants 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).\n\nThe primary outcome is the IPV rate against infertile women over the past 12 months.",[154,30],"Infertility, Female","2024-08-26",{"date":157,"type":39},"2024-08-28",{"date":159,"type":39},"2024-06-25",{"date":161,"type":21},"2026-07",{"name":163,"class":46},"Peking University Third Hospital",{"id":165,"slug":166,"hasResults":11,"nctId":167,"briefTitle":168,"officialTitle":169,"acronym":4,"eligibilityCriteria":170,"healthyVolunteers":16,"sex":17,"minAge":171,"maxAge":18,"enrollmentInfo":172,"targetDuration":4,"studyType":22,"phases":174,"briefSummary":175,"conditions":176,"keywords":177,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":179,"lastUpdatePostDateStruct":180,"startDateStruct":182,"completionDateStruct":184,"leadSponsor":186,"locationsCount":47},"100380572","healing-circles-an-intervention-for-canadian-indigenous-mothers--children-affected-by-ipv-100380572","NCT04235335","Healing Circles: An Intervention for Canadian Indigenous Mothers & Children Affected by IPV","Healing Circles: An Evaluation of an Intervention for Canadian Indigenous Mothers and Children Affected by Intimate Partner Violence","Inclusion Criteria:\n\n* mothers self-reported experience of past intimate partner violence, English-speaking, with at least one school-aged child\n\nExclusion Criteria:\n\n\\-","6 Years",{"count":173,"type":21},160,[24],"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",[30],[68,178],"exposure to violence","2024-03-13",{"date":181,"type":39},"2024-03-15",{"date":183,"type":39},"2024-02-23",{"date":185,"type":21},"2026-07-30",{"name":187,"class":46},"University of Manitoba"]