[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"intimate-partner-violence\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:intimate-partner-violence":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,12,0,[8,46,69,99,126,148,171,195,222,250,275,303],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100556526","evaluating-interventions-for-intimate-partner-violence-use-in-washington-state-100556526",false,"NCT06526247","Evaluating Interventions for Intimate Partner Violence Use in Washington State","Inclusion Criteria:\n\nMen:\n\n1. Identify as a man\n2. Provide consent for the research team to contact his intimate partner(s) for data collection purposes;\n3. Court-referred for IPV intervention in Washington state\n\nWomen:\n\n1. Identify as a woman\n2. Were or currently are an intimate partner involved in an incident of IPV with a court-referred participant\n\nExclusion Criteria:\n\n1. demonstrates active psychosis that may interfere with their ability to participate in group\n2. expresses prominent suicidal or homicidal ideation that requires hospitalization\n3. does not possess proficiency in spoken English\n4. periods of incarceration after study enrollment","ALL","18 Years",{"count":18,"type":19},800,"ESTIMATED","INTERVENTIONAL",[22],"NA","Intimate partner violence (IPV), specifically physical and psychological aggression toward an intimate partner, represents a public health crisis that affects millions of Americans each year. There currently exists very little evidence from randomized controlled trials for the effectiveness of abuser intervention programs designed to prevent and end perpetration of IPV in the general population. This is troubling considering that approximately half a million men and women are court-mandated to these programs each year.\n\nThe investigators will conduct a randomized controlled non-inferiority trial evaluating the effectiveness of the Strength at Home (SAH) intervention in reducing intimate partner violence (IPV). The overarching aim of this study is to determine whether outcomes achieved through SAH are non-inferior to those achieved through standard IPV interventions offered in the state of Washington (treatment as usual; TAU) among court-involved men who have used IPV.\n\nThe specific aims are:\n\n1.1: Compare the frequency of physical and psychological IPV, the primary outcomes of interest, across conditions as reported by the male participants and their intimate partners across Time 1 (baseline) and four 3-month follow ups (Times 2-5). It is expected that reductions in physical and psychological IPV perpetration observed in SAH will be non-inferior to those observed in TAU over the course of the year.\n\n1.2: Compare symptoms of PTSD, alexithymia, and alcohol use problems across conditions and assessment time points as reported by the male participants. It is expected that reductions in PTSD symptoms, alexithymia, and alcohol use problems observed in SAH will be non-inferior to those observed in TAU over the course of the year.\n\n1.3: Compare treatment satisfaction across conditions as reported by the male participants across the four 3-month follow ups (Times 2-5). It is expected that treatment satisfaction in SAH will be comparable to or greater than treatment satisfaction in TAU.",[25],"Intimate Partner Violence",[27,28,29,30,31,32],"Strength at Home (SAH)","Trauma-informed","Treatment as Usual (TAU)","Posttraumatic stress disorder (PTSD)","Alcohol use","Washington state","RECRUITING","2026-06-18",{"date":36,"type":37},"2026-06-23","ACTUAL",{"date":39,"type":37},"2024-11-18",{"date":41,"type":19},"2027-07",{"name":43,"class":44},"Boston University","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":54,"minAge":16,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":20,"phases":57,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":45},"100469112","domestic-violence-enhanced-perinatal-care-program-in-china-100469112","NCT05388565","Domestic Violence Enhanced Perinatal Care Program in China","Testing the Domestic Violence Enhanced Perinatal Care in China","Inclusion Criteria:\n\n* Being in early pregnancy (less than 13 weeks gestation) and screened positive for IPV in the year before pregnancy or during the current pregnancy.\n\nExclusion Criteria:\n\n* Women who are not able to read and understand Chinese.",true,"FEMALE",{"count":56,"type":19},100,[22],"The proposed project addresses intimate partner violence (IPV) against pregnant women, which is a serious social and health issue. Pregnant women represent a particularly vulnerable population of IPV survivors in China, who have been largely underserved. There have been no interventions developed in China to prevent maternal IPV and its effects on maternal and infant health. The proposed project is the first structured IPV intervention integrated into prenatal care in China, which may have the potential to be translated into more prenatal clinics in China to prevent violence against pregnant women and improve maternal and infant health.",[25],"2026-06-06",{"date":62,"type":37},"2026-06-09",{"date":64,"type":37},"2023-02-25",{"date":66,"type":19},"2026-10-30",{"name":68,"class":44},"University of Texas at Austin",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":73,"acronym":74,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":54,"minAge":16,"maxAge":4,"enrollmentInfo":76,"targetDuration":4,"studyType":20,"phases":78,"briefSummary":79,"conditions":80,"keywords":82,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":45},"100639220","shame-resilience-and-well-being-after-intimate-partner-violence-an-intervention-study-with-replicated-single-subject-design-100639220","NCT07618754","Shame, Resilience and Well-being After Intimate Partner Violence: an Intervention Study With Replicated Single-Subject Design.","EMBER-4","Inclusion Criteria:\n\n* subjected to IPV within 2 years prior to enrollment\n* capable of completing questionnaires using a mobile phone\n* intention to complete intervention\n* identifies as female\n\nExclusion Criteria:\n\n* ongoing severe IPV\n* ongoing severe substance use\n* psychosis\n* moderate to severe suicidality\n* ongoing psychological intervention in other facility",{"count":77,"type":19},8,[22],"The EMBER protocol is a health care method that is designed to increase resilience, in order to improve well-being and overall health in women who have experienced violence by a partner. This study explores whether the EMBER intervention works in this way. Eight participants will take part in the EMBER program and complete questionnaires every week during the intervention. The researchers will compare the timeline for the intervention to how resilience levels change. They will also check whether changes in resilience are linked to changes in health and well-being.",[25,81],"Resilience, Psychological",[83,25,84,85,86,87,88],"Single Case Design","Domestic Violence","Domestic Violence and Abuse","Resilience, psychological","Trauma","Well-Being","NOT_YET_RECRUITING","2026-05-25",{"date":92,"type":37},"2026-06-01",{"date":94,"type":19},"2026-06",{"date":96,"type":19},"2030-06",{"name":98,"class":44},"Uppsala University",{"id":100,"slug":101,"hasResults":11,"nctId":102,"briefTitle":103,"officialTitle":103,"acronym":104,"eligibilityCriteria":105,"healthyVolunteers":11,"sex":54,"minAge":16,"maxAge":4,"enrollmentInfo":106,"targetDuration":4,"studyType":108,"phases":4,"briefSummary":109,"conditions":110,"keywords":114,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":125,"locationsCount":45},"100640395","resilience-and-recovery-after-intimate-partner-violence---evaluation-of-the-ember-ipv-protocol-100640395","NCT07606586","Resilience and Recovery After Intimate Partner Violence - Evaluation of the EMBER-IPV Protocol","EMBER-3","Inclusion Criteria:\n\n* Women taking part of the EMBER intervention (phase A or C)\n* Subjected to IPV within the past 2 years prior to enrollment\n\nExclusion Criteria:\n\n* Ongoing severe intimate partner violence\n* Ongoing severe substance abuse\n* Severe mental health problems such as psychosis, suicidality",{"count":107,"type":19},150,"OBSERVATIONAL","The EMBER-protocol is an intervention used at the NCK clinic at Uppsala University Hospital with the purpose of helping women utilize their resilience and strengths in order to recover after intimate partner violence. This study is conducted in order to explore how health and resilience changes during the course of the EMBER-intervention. The participants are asked to complete questionnaires before, during and after the intervention.",[25,111,112,113,81],"Intimate Partner Violence Against Women","Shame","Domestic Abuse",[25,84,115,116,112,86,117],"domestic violence exposure","gender-based violence","resilience intervention","2026-05-18",{"date":120,"type":37},"2026-05-26",{"date":122,"type":19},"2026-05",{"date":124,"type":19},"2029-04",{"name":98,"class":44},{"id":127,"slug":128,"hasResults":11,"nctId":129,"briefTitle":130,"officialTitle":131,"acronym":4,"eligibilityCriteria":132,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":133,"targetDuration":4,"studyType":20,"phases":135,"briefSummary":136,"conditions":137,"keywords":4,"overallStatus":89,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":147},"100578486","the-primary-prevention-of-intimate-partner-violence-100578486","NCT06811922","The Primary Prevention of Intimate Partner Violence","Primary Prevention of Intimate Partner Violence","Inclusion Criteria:\n\n* couples wherein both members are age ≥18 years,\n* married ≤ 1 year, in their first marriage, married to only one individual, cohabiting in a slum in Mumbai or Pune India, and\n* fluent in Marathi and\u002For Hindi\n* Both members of the couple must meet eligibility criteria and be present at the session for the couple to participate.\n\nExclusion Criteria:\n\n* As GBE was designed for primary IPV prevention, couples in which the female member screens positive for physical and\u002For sexual IPV (using the modified Conflict Tactics Scale (CTS-2)) at baseline will be excluded (and referred to support services)\n* those in the 3rd trimester of pregnancy (as women traditionally return to their natal home during this perinatal period).",{"count":134,"type":19},1700,[22],"This is a cluster randomized trial for newly married dyads, that seeks to quantify the impact of GBE's (Ghya Bharaari Ekatra's) intervention on intimate partner violence (IPV) and downstream outcomes, mental health and reproductive autonomy, examine its mechanism of action, contexts in which it may need modification, and factors associated with its future successful adoption and implementation.",[25],"2026-04-28",{"date":140,"type":37},"2026-05-04",{"date":142,"type":19},"2026-10",{"date":144,"type":19},"2027-10",{"name":146,"class":44},"Emory University",2,{"id":149,"slug":150,"hasResults":11,"nctId":151,"briefTitle":152,"officialTitle":153,"acronym":154,"eligibilityCriteria":155,"healthyVolunteers":53,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":156,"targetDuration":4,"studyType":20,"phases":158,"briefSummary":159,"conditions":160,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":167,"leadSponsor":169,"locationsCount":147},"100521782","father-focused-intervention-for-reducing-family-violence-and-symptoms-in-children-100521782","NCT06074068","Father-Focused Intervention for Reducing Family Violence and Symptoms in Children","Examining Therapeutic Change Mechanisms in an Affect Regulation, Father-Focused Intervention for Reducing Family Violence and Associated Symptoms in Children","F4C","Inclusion Criteria:\n\n* have at least one 6 month to 12-year-old biological child with whom they have contact;\n* had an incident of IPV within the last 12 months prior to screening with their child's mother (based on court\u002Fpolice records, coparent or self-report);\n* have a currently open or recently investigated (in the last 6 months) case with CT DCF\n* are able to complete assessments in English or Spanish;\n* agree to have their female coparents (mother of target child) contacted as collateral informants and for consent for participation of their child. If a participant has more than one child in the age range, the youngest will be selected;\n* female coparents (i.e., biological mother who need not be in a relationship with the father) consents to (at minimum) provide parent-report on child; however, may opt out of child participation. If the coparent agrees to participate by providing caregiver-report on child symptoms, but declines participation of their shared child, the father may still participate in the study if he meets eligibility criteria outlined below; thus, preventing any possible retaliation against co-parents for not consenting to child participation.\n\nExclusion Criteria:\n\nFathers will be excluded based on the following exclusion criteria:\n\n* an active full\u002Fno contact protective order pertaining to their child because this will preclude participation in the father-child play assessment (many men will have protective orders pertaining to their partners, but it is more common for men to still be allowed contact with their children);\n* physiological addiction to a substance that requires detoxification. Fathers will be evaluated using the Drug Abuse Screening Test and AUDIT. If fathers report significant difficulties with physiological withdrawal (e.g., alcohol tremors or dope sickness) they will be referred for detox services. They can be re-evaluated following a detox program with documentation from the detox center of successful completion and clean urine screen;\n* cognitive impairment that will not allow for understanding of the study interventions (a mini mental state score \\\u003C25);\n* current untreated psychotic disorder;\n* currently suicidal or homicidal ideation based on screening using the BSI; or\n* previously participated in F4C or a BIP.",{"count":157,"type":19},1080,[22],"The goal of this clinical trial is to test the efficacy of Fathers for Change (F4C) compared to standard Batterer Intervention for fathers with a history of Intimate Partner Violence. The main question\\[s\\] it aims to answer are:\n\n1. Is F4C more efficacious than standard BIP in reducing family violence and child mental health impairment?\n2. What are the trajectories of therapeutic change targets across interventions?\n3. Does father's emotion regulation and reflective functioning mediate the relationship between the two interventions and child-related outcomes? Participants will be randomized to either Fathers for Change on Batterer Intervention.",[25,161],"Child Maltreatment","2026-04-10",{"date":164,"type":37},"2026-04-15",{"date":166,"type":37},"2024-01-11",{"date":168,"type":19},"2028-12-31",{"name":170,"class":44},"Yale University",{"id":172,"slug":173,"hasResults":11,"nctId":174,"briefTitle":175,"officialTitle":176,"acronym":177,"eligibilityCriteria":178,"healthyVolunteers":11,"sex":54,"minAge":16,"maxAge":4,"enrollmentInfo":179,"targetDuration":4,"studyType":108,"phases":4,"briefSummary":181,"conditions":182,"keywords":184,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":187,"lastUpdatePostDateStruct":188,"startDateStruct":190,"completionDateStruct":192,"leadSponsor":194,"locationsCount":45},"100611064","how-a-resilience-focused-intervention-is-perceived-by-women-subjected-to-domestic-violence-100611064","NCT07235722","How a Resilience-Focused Intervention is Perceived by Women Subjected to Domestic Violence","Exploring Resilience. A Qualitative Study of an Intervention After Intimate Partner Violence.","EMBER-2","Inclusion Criteria:\n\n* Enrolled in the EMBER intervention at the NCK outpatient clinic.\n\nExclusion Criteria:\n\n* Any situation that, in the opinion of the Investigator, would compromise the safety of the patient or the quality of the data.",{"count":180,"type":19},30,"At Uppsala University Hospital, there is an outpatient clinic for women subjected to intimate partner violence. In order to explore how patients experience the biopsychosocial resilience-based intervention in use at the clinic and how well the intervention fits the needs of the patients, 30 patients from different stages of their contact at the clinic and with diverse life situations and background are enrolled. The researchers will carry out individual in-person interviews, each lasting approximately 60 minutes, based on a semi-structured set of questions. The questions concern the participant´s life situation, resilience and self-perceived needs, how well the intervention has met those needs and how it was perceived by the participant. The interviews are audio-recorded and transcribed verbatim for thematic analysis.",[112,25,183,81],"Domestic Violence Exposure",[185,186,25,84,115,116,112,81],"Qualitative","interview","2026-04-08",{"date":189,"type":37},"2026-04-13",{"date":191,"type":37},"2026-04-07",{"date":193,"type":19},"2027-03",{"name":98,"class":44},{"id":196,"slug":197,"hasResults":11,"nctId":198,"briefTitle":199,"officialTitle":200,"acronym":4,"eligibilityCriteria":201,"healthyVolunteers":53,"sex":15,"minAge":202,"maxAge":203,"enrollmentInfo":204,"targetDuration":4,"studyType":20,"phases":206,"briefSummary":207,"conditions":208,"keywords":210,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":213,"lastUpdatePostDateStruct":214,"startDateStruct":216,"completionDateStruct":218,"leadSponsor":220,"locationsCount":45},"100610347","virtual-village-for-young-parents-100610347","NCT07226401","Virtual Village for Young Parents","Preventing Intimate Partner Violence Among Teens Who Are Pregnant or Parenting","Inclusion Criteria:\n\nPregnant or parenting youth (Pilot RCT participants)\n\n* Aged 16-21 years.\n* Currently pregnant, partner of a pregnant person, or parenting a child (i.e., have contact with child at least once per week).\n* Able to speak and read English.\n* Willing and able to provide written informed consent.\n* Willing and able to provide adequate contact\u002Flocator information.\n\nFacilitators (IDI participants)\n\n* Aged 18 years or older.\n* Trained and served as a facilitator of the virtual SDYP intervention.\n* Able to speak and read English.\n* Able and willing to provide verbal informed consent.\n\nExclusion Criteria (Pilot RCT participants):\n\n* Has any other condition that, in the opinion of the PI or their designee, would preclude informed consent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.\n* Currently participating or will be participating in a violence prevention education program in the next 3 months.\n* Previously participated in the Empowering Young Parents study.","16 Years","21 Years",{"count":205,"type":19},80,[22],"This project will study virtual delivery of Safe Dates for Young Parents (SDYP), a 10-session, group-based intimate partner violence (IPV) prevention program tailored for adolescents and young adults who are pregnant or parenting. This program has the potential to improve the health and well-being of young parents and their children, and virtual delivery may improve participants' ability to attend. The main questions it aims to answer are: (1) Is it feasible and acceptable to implement SDYP in a virtual setting? (2) Are SDYP participants less likely to experience IPV than participants in an alternate health education program? Participants will be invited to a series of virtual program sessions for either SDYP or a health education program focused on physical activity and nutrition and will be asked to complete surveys before the programs begin and up to 6 months later.",[209,25],"Gender-based Violence",[211,212],"Young Adult Parents","Adolescent Pregnancy","2025-12-09",{"date":215,"type":37},"2025-12-15",{"date":217,"type":37},"2025-11-11",{"date":219,"type":19},"2026-07-31",{"name":221,"class":44},"RTI International",{"id":223,"slug":224,"hasResults":11,"nctId":225,"briefTitle":226,"officialTitle":226,"acronym":227,"eligibilityCriteria":228,"healthyVolunteers":11,"sex":54,"minAge":16,"maxAge":4,"enrollmentInfo":229,"targetDuration":4,"studyType":20,"phases":231,"briefSummary":232,"conditions":233,"keywords":237,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":241,"lastUpdatePostDateStruct":242,"startDateStruct":244,"completionDateStruct":246,"leadSponsor":248,"locationsCount":45},"100592081","multifaceted-intervention-to-restore-resilience-and-overcome-risk-100592081","NCT06988787","Multifaceted Intervention to Restore Resilience and Overcome Risk","MIRROR","Inclusion Criteria:\n\n* Able to consent as determined by UBACC, are English-speaking FVets who are 18+ years old\n* Screen positive for exposure to IPV and\u002For MST using the VA Intimate Partner Violence Assistance Program (VA IPVAP) and MST Screening Protocol,\n* Have a history of at least one BI assessed using the BISQ+IPV,\n* Sub-threshold PTSD (operationalized as a total score of \\>33 on the PTSD Checklist Diagnostic and Statistical Manual of Mental Disorders-5 (PCL-5),\n* Report deficits in Emotion Regulation (operationalized as a score of 0.5 SD above published means on the DERS).\n\nExclusion Criteria:\n\n* FVets at high risk for suicide (respond yes to items 3, 4, 5, or 8 on the Columbia Suicide Severity Rating Scale \\[C-SSRS\\]),\n* Observable active psychosis (e.g., auditory hallucinations, grandiose delusions),\n* Those determined to have problematic substance use (score \\> 27 on the Alcohol, Smoking and Substance Involvement Screening Test (ASSIST) will be referred to substance use dependence programs for concurrent treatment. The PI and Co-Is will collaborate with the substance use dependence program to determine continued participation.",{"count":230,"type":19},136,[22],"The MIRROR study will compare the effectiveness of two interventions in improving emotion regulation and reducing PTSD symptoms in female Veterans with military sexual trauma (MST) and\u002For intimate partner violence (IPV) and co-occurring brain injury.",[234,25,235,236],"Military Sexual Trauma","Brain Injury","Post Traumatic Stress Disorder",[234,25,238,239,235,240],"Female Veterans","Emotion Regulation","Exposure Therapy","2025-12-03",{"date":243,"type":37},"2025-12-10",{"date":245,"type":37},"2025-09-12",{"date":247,"type":19},"2028-08-01",{"name":249,"class":44},"Icahn School of Medicine at Mount Sinai",{"id":251,"slug":252,"hasResults":11,"nctId":253,"briefTitle":254,"officialTitle":255,"acronym":256,"eligibilityCriteria":257,"healthyVolunteers":53,"sex":54,"minAge":258,"maxAge":203,"enrollmentInfo":259,"targetDuration":4,"studyType":20,"phases":261,"briefSummary":262,"conditions":263,"keywords":264,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":267,"lastUpdatePostDateStruct":268,"startDateStruct":270,"completionDateStruct":272,"leadSponsor":274,"locationsCount":5},"100560365","empowering-young-parents-building-healthy-relationships-study-100560365","NCT06576193","Empowering Young Parents: Building Healthy Relationships Study","Empowering Young Parents: Building Health Relationships Study Evaluation of the Safe Dates for Young Parents Intervention","EYP","Inclusion Criteria:\n\nAdolescent and Young Adult (AYA) \\[EYP study participants\\]\n\n* Aged 14-21 years (inclusive) at Screening.\n* Assigned female sex at birth.\n* Currently pregnant or parenting their child who lives with them at least part-time.\n* Able to speak and read English or Spanish.\n* Able and willing to provide verbal informed consent for enrollment in the EYP study.\n* Able and willing to provide adequate contact\u002Flocator information.\n* Able and willing to complete protocol requirements, including completion of three study interviews over one year.\n\nStudy Facilitators (process evaluation participants)\n\n* Aged 18 years or older.\n* Trained and served as a facilitator of the SDYP intervention.\n* Able to speak and read English.\n* Able and willing to provide verbal informed consent.\n\nExclusion Criteria:\n\n* Per participant report at Screening or Enrollment, intends to travel away from their geographic area of residence for a time period that would interfere with study participation, including with intervention participation should the participant be randomized to the SDYP intervention.\n* Has any other condition that, in the opinion of the Principal Investigator (PI) or their designee, would preclude informed consent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.","14 Years",{"count":260,"type":19},600,[22],"The goal of this trial is to learn how the Safe Dates for Young Parents (SDYP) intervention affects the sexual and reproductive health behaviors, and quality of, and attitudes surrounding intimate partner relationships in adolescents and young adults (AYA) assigned female sex at birth who are pregnant or parenting.\n\nThe main questions it aims to answer are:\n\n* Will the SDYP intervention have any effect on the sexual and reproductive health behaviors during the study period?\n* Will the SDYP intervention have any effect on the prevention or reduction of intimate partner violence (IPV)?\n* Will the SDYP intervention have any effect on the attitudes and beliefs about healthy relationships?\n\nResearchers will compare the behaviors, attitudes, and beliefs about sexual and reproductive health and relationships of participants assigned to the SDYP intervention group to participants assigned to the control (non-SDYP intervention) group to see if there is any difference or changes in those behaviors, attitudes, and beliefs before-and-after or without the SDYP intervention.\n\nParticipants in the SDYP intervention will attend ten (10) 50-minute group sessions that will involve interactive discussions, thinking through life-like scenarios, games, role-plays, brainstorming, and a poster contest and theatrical play.",[209,25],[211,212,265,266],"Adolescent Parents","Healthy Relationships","2025-10-28",{"date":269,"type":37},"2025-10-30",{"date":271,"type":37},"2024-10-16",{"date":273,"type":19},"2028-08",{"name":221,"class":44},{"id":276,"slug":277,"hasResults":11,"nctId":278,"briefTitle":279,"officialTitle":280,"acronym":281,"eligibilityCriteria":282,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":283,"targetDuration":4,"studyType":20,"phases":284,"briefSummary":285,"conditions":286,"keywords":288,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":294,"lastUpdatePostDateStruct":295,"startDateStruct":297,"completionDateStruct":299,"leadSponsor":301,"locationsCount":45},"100507891","harmony-a-combined-mi-and-bct-intervention-to-reduce-intimate-partner-violence-and-alcohol-use-in-south-india-100507891","NCT05893277","Harmony: A Combined MI and BCT Intervention to Reduce Intimate Partner Violence and Alcohol Use in South India","A Combined Motivational Interviewing and Behavioral Couples Therapy Intervention to Reduce Intimate Partner Violence and Alcohol Use in South India","Harmony","Inclusion Criteria:\n\n1. married couple with both spouses age ≥18;\n2. living within the catchment area of the PHC (primary health center);\n3. speaking Kannada or Hindi;\n4. wife reporting any physical or sexual intimate partner violence (IPV) in the past 12 months (note exclusion for severe IPV below);\n5. the husband having Alcohol Use Disorder (AUD) measured by AUDIT-C (AUDIT-C ≥4).\n\nExclusion Criteria:\n\n1. husband has severe alcohol dependency (per Severity of Alcohol Dependence Questionnaire, SADQ ≥ 31) or is at risk of severe withdrawal symptoms (Clinical Institute Withdrawal Assessment for Alcohol Scale-Revised - CIWA-AR);\n2. significant medical problems that will make the couple unable to participate in the intervention sessions;\n3. cognitive problems (adapted Short-Blessed Cognitive Test score ≤7);\n4. past year history of IPV severe enough to result in hospitalization (per an adapted version of the International Violence Against Women Survey - IVAWS), or 5) wife screens positive for any AUD (AUDIT-C \\>4).",{"count":18,"type":19},[22],"The goal of this randomized clinical trial is to test an intervention consisting of a combination of behavioral couples therapy and motivational interviewing to improve communication and reduce conflicts between couples and decrease harmful drinking among spouses in urban primary health centers, South India. The intervention will be delivered by nurses in primary health centers who will be supervised by a clinical psychologist.\n\nThe main question\\[s\\] it aims to answer are:\n\n* Do the wives of the couples in the intervention report less intimate partner violence (IPV) after 12 months, compared to wives in couples in a control group?\n* Do the husbands of the couples in the intervention show less alcohol consumption after 12 months, compared to husbands in couples in a control group? Husbands will participate in Motivational Interview (MI) sessions targeted at reducing their alcohol use. Husband and wife will participate in Behavioral Couples Therapy (BCT) targeted at improving their marital relationship.\n\nThese intervention participants will be compared to a control group who will receive only referral information for intimate partner violence and an educational session and referral for alcohol use disorder.\n\nAll participants will participate in quantitative interviews at baseline, and every three months thereafter, for a period of one year. In-depth qualitative interviews will be done with a subgroup of couples to try to understand how the intervention led to the observed outcomes.",[25,287],"Alcohol Use Disorder",[289,290,291,292,293],"Randomized Controlled Trial","Motivational Interviewing","Behavioral Couples Therapy","India","Nurse-delivered intervention","2025-07-02",{"date":296,"type":37},"2025-07-04",{"date":298,"type":37},"2023-10-12",{"date":300,"type":19},"2027-05-31",{"name":302,"class":44},"University of California, San Francisco",{"id":304,"slug":305,"hasResults":11,"nctId":306,"briefTitle":307,"officialTitle":308,"acronym":4,"eligibilityCriteria":309,"healthyVolunteers":53,"sex":54,"minAge":16,"maxAge":310,"enrollmentInfo":311,"targetDuration":4,"studyType":20,"phases":313,"briefSummary":314,"conditions":315,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":316,"lastUpdatePostDateStruct":317,"startDateStruct":319,"completionDateStruct":321,"leadSponsor":323,"locationsCount":45},"100504110","perceptions-of-trauma-and-violence-informed-care-100504110","NCT05844020","Perceptions of Trauma and Violence Informed Care","Assessment of Survivor and Provider Perceptions of Trauma and Violence Informed Care Among Black Women","Inclusion Criteria:\n\n* Meharry or Matthew Walker Comprehensive Health Center female patients\n* Self-identify as Black\n* Self-identify as intimate partner violence survivors\n* English or Spanish language fluency\n\nExclusion Criteria:\n\n* Not Black female intimate partner violence survivor of Meharry or Matthew Walker Comprehensive Health Center\n* Those without English or Spanish language fluency","79 Years",{"count":312,"type":19},250,[22],"The purpose of this study is to adapt, implement and evaluate a trauma and violence informed care intervention designed for Black women in middle Tennessee.",[25],"2025-05-07",{"date":318,"type":37},"2025-05-13",{"date":320,"type":37},"2023-04-17",{"date":322,"type":19},"2027-08-31",{"name":324,"class":44},"Meharry Medical College"]