[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"intimate-partner-violence-ipv\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:intimate-partner-violence-ipv":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,19,0,[8,46,78,103,130,161,190,219,246,274,298,328,355,379,400,436,463,493,517],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100644226","pre-pilot-wings-mhealth-to-improve-moud-uptake-in-women-experiencing-intimate-partner-violence-and-ptsd-100644226",false,"NCT07665502","Pre-Pilot WINGS+++: mHealth to Improve MOUD Uptake in Women Experiencing Intimate Partner Violence and PTSD","Pre-Pilot WINGS +++ An Effectiveness Trial of Syndemic Mhealth Intervention to Increase MOUD Uptake Among Women Impacted by Intimate Partner Violence and PTSD","Inclusion Criteria:\n\n* Identify as a woman (cis-gender or transgender)\n* Aged 18 or older\n* Report use of non-prescribed opioids in the past 30 days\n* Score positive for risk of opioid use disorder or other substance use disorder on the Drug Abuse Screening Test (DAST) with a cut-off score of 6 or higher\n* Report experiencing any severe psychological abuse or any physical or sexual abuse by a female or male intimate partner in the past year\n\nExclusion Criteria:\n\n* Evidence of significant psychiatric or cognitive impairment that would limit effective participation, as confirmed during informed consent\n* Inability to speak and understand English sufficiently to participate in assessments or intervention sessions","FEMALE","18 Years",{"count":19,"type":20},7,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this pre-pilot for the clinical trial is to develop a mobile health (mHealth) program called WINGS+++ can help women with opioid use disorder or other substance use disorders who have experienced intimate partner violence. The pre-pilot study will take place in Orange County, New York with n=7 women. .\n\nThe main questions it aims to answer are:\n\n1. Does WINGS+++ lower non-prescription opioid and other drug use in women?\n2. Does WINGS+++ help connect women to treatment for substance use, intimate partner violence, and post-traumatic stress disorder (PTSD)?\n\nResearchers will compare WINGS+++ to standard care to see if WINGS+++ works better to lower drug use and link women to helpful services.\n\nWINGS+++ is a 3-session program on a mobile device that:\n\n* Screens for intimate partner violence, PTSD, and substance use\n* Offers brief support and referrals based on each woman's needs and preferences\n* Connects women to a peer navigator who helps link them to services\n\nParticipants will:\n\n* Take part in only the WINGS+++ program for the pre-pilot\n* Answer survey questions about drug use, intimate partner violence, and PTSD symptoms\n* Provide biological samples (such as urine or hair) to check for drug use\n* Share information about the services they have used",[26,27,28,29,30,31,32],"Opioid-Related Disorders","Substance-Related Disorders","Intimate Partner Violence (IPV)","Stress Disorders, Post-Traumatic","Domestic Violence","Medication for Opioid Use Disorder (MOUD)","Post Traumatic Stress Disorder PTSD","NOT_YET_RECRUITING","2026-06-18",{"date":36,"type":37},"2026-06-24","ACTUAL",{"date":39,"type":20},"2026-06-15",{"date":41,"type":20},"2027-08-31",{"name":43,"class":44},"Dawn A. Goddard-Eckrich","OTHER",2,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":54,"minAge":4,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":58,"conditions":59,"keywords":60,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":77},"100639700","familia-imara-a-parenting-program-to-reduce-family-violence-in-tanzania-100639700","NCT07574567","Familia Imara: A Parenting Program to Reduce Family Violence in Tanzania","Cluster Randomized Controlled Trial to Assess the Effectiveness of Familia Imara in Preventing Violence Against Women and Children and Improving Child Nutrition and Development in Tanzania","Inclusion Criteria:\n\n* The household has a child aged 0-24 months at enrollment\n* The child has a primary female caregiver (i.e., mother) and a primary male caregiver (i.e., father) who are in a partnered relationship\n* Primary female caregiver, primary male caregiver, and child reside together in the same household\n* Both caregivers provide written informed consent for themselves and their child to participate in the study\n\nExclusion Criteria:\n\n* Need to satisfy the inclusion criteria\n* Expecting to relocate in the next year",true,"ALL",{"count":56,"type":20},6216,[23],"This cluster-randomized controlled trial will evaluate the effectiveness, implementation, and scalability of Familia Imara, a group-based, couples-focused, community health worker (CHW)-delivered parenting program, on reducing intimate partner violence (IPV), harsh discipline, and improving child development and nutrition outcomes in the Mara and Geita regions of Tanzania. Villages will be randomly assigned to either an intervention or control arm. The study will be implemented in two sequential cohorts. In Cohort 1, a traditional randomized controlled trial will compare intervention villages receiving the program to control villages receiving no intervention (waitlist control), with delivery supported primarily by implementing partners in collaboration with government supervisors. In Cohort 2, the same villages will retain their original assignment. Intervention villages will receive the program under a government-led delivery model to assess scalability and integration into existing systems, while control villages will transition from waitlist to receive the intervention. Evidence generated will inform policy and practice for preventing family violence and promoting early childhood development at scale.",[28],[61,62,63,64,65,66],"Intimate Partner Violence","Couples","Parenting","Harsh Discipline","Early Childhood Development","Nutrition","RECRUITING","2026-06-03",{"date":70,"type":37},"2026-06-04",{"date":72,"type":37},"2026-05-02",{"date":74,"type":20},"2028-04-01",{"name":76,"class":44},"Saini Das",1,{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":21,"phases":87,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":97,"completionDateStruct":98,"leadSponsor":100,"locationsCount":102},"100601787","project-stronger-stepped-care-for-opioid-use-disorder-treatment-engagement-and-recovery-100601787","NCT07115030","Project STRONGER: Stepped Care for Opioid Use Disorder Treatment Engagement and Recovery","STRONGER","Inclusion Criteria:\n\n* Woman;\n* Are ≥ 18 years old;\n* Receive MOUD treatment at one of the participating sites;\n* Have received MOUD for \\>14 days to allow for initial stabilization;\n* Have initiated the current treatment episode within the past 12 months;\n* Experienced physical or psychological IPV in their lifetime;\n* Have at least moderate impairment in psychosocial functioning (on B-IPF) as a result of PTSD symptoms;\n* Available during the date\u002Ftime of the intervention group\n* Able to read\u002Funderstand English; and\n* Provide written informed consent.\n\nExclusion Criteria:\n\n* Fail a capacity-to-consent questionnaire;\n* Have an unstable medical condition (e.g., hospitalization, planned surgery, newly starting chemotherapy, plans for palliative care) and\u002For unstable psychiatric illness (e.g., untreated psychosis) that would interfere with their ability to participate in study activities;\n* Will be unavailable for \\>4 consecutive weeks during the study period (e.g., anticipated move, planned surgery);\n* Are unable to read\u002Funderstand English;\n* Inability to provide at least one form of contact",{"count":86,"type":20},532,[23],"Using a hybrid type 1 effectiveness-implementation approach, this study aims to evaluate the impact of a novel stepped care model (\"PCT+2HOPE\") versus treatment as usual (TAU) on increasing retention in community-based medication for opioid use disorder (MOUD) treatment among women who have experienced intimate partner violence (W-IPV). PCT+2HOPE includes Present-Centered Therapy (PCT+) with stepped care as indicated by moderate, severe, or extreme PTSD-related impairment in psychosocial functioning to Helping to Overcome PTSD through Empowerment (HOPE), two evidence-based behavioral interventions adapted for women with opioid use disorder (OUD). We will examine the effectiveness of PCT+2HOPE vs. TAU on the primary outcome (i.e., retention in MOUD treatment) and secondary outcomes related to trauma (i.e., PTSD-related impairment in psychosocial functioning and depression), substance use (i.e. OUD symptom severity, extra-medical opioid use \\[i.e., use of prescription opioids without a doctor's prescription; in greater amounts, more often, longer than prescribed, or for a reason other than a doctor said they should be used\\], and recovery), and empowerment. We will explore the extent to which the effectiveness of PCT+2HOPE vs. treatment as usual differs based on access to basic needs. We will also conduct an implementation-focused process evaluation.",[90,28,32],"Opioid Use Disorder",[92,93,94],"opioid use disorder","intimate partner violence","domestic violence","2026-06-01",{"date":68,"type":37},{"date":95,"type":37},{"date":99,"type":20},"2029-08-31",{"name":101,"class":44},"Yale University",3,{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":107,"acronym":108,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":54,"minAge":17,"maxAge":110,"enrollmentInfo":111,"targetDuration":4,"studyType":21,"phases":113,"briefSummary":115,"conditions":116,"keywords":117,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":45},"100584181","phase-2-psilocybin-assisted-therapy-for-post-traumatic-stress-disorder-in-survivors-of-intimate-partner-violence-100584181","NCT06885996","Psilocybin-assisted Therapy for Post-Traumatic Stress Disorder in Survivors of Intimate Partner Violence","PsiPTSD","Inclusion Criteria:\n\n* Individuals of all sexes, gender identities, and ethnicities\n* Ages 19 to 65 years at the time of screening\n* At least 6 months since last IPV incident\n* A score of 1 on the Composite Abuse Scale with repetition of abusive events\n* Minimum PCL-5 score of ≥ 33\n* Limited lifetime use of serotonergic hallucinogens\n* Ability to read\u002Fwrite English\n\nExclusion Criteria:\n\n* Severe or moderate substance use disorder other than nicotine in past 6 months\n* Lifetime diagnosis of schizophrenia or bipolar disorders (or first or second-degree relative)\n* Active suicidal ideation or serious attempt within the past 1 year.\n* Current pregnancy or nursing, trying to become pregnant\n* Any notable abnormality on ECG or routine medical blood laboratory test\n* Insulin-dependent diabetes; if taking oral hypoglycemic agent, then no history of hypoglycemia\n* Epilepsy with a history of seizures\n* Current or recent (within 12 weeks) participation in a clinical trial\n* Cognitive impairment (SLUMS score \\\u003C20)\n* Suffered a moderate\u002Fsevere TBI at least once in lifetime\n* Suffered a mild TBI within the last 6 months\n* Any other circumstances that, in the opinion of the investigators, compromises participant safety\n* Not compelled to enter treatment to avoid legal consequences","65 Years",{"count":112,"type":20},76,[114],"PHASE2","The goal of this randomized controlled trial is to evaluate the efficacy of psilocybin administered with Acceptance and Commitment Therapy (ACT) as an intervention to reduce post-traumatic stress disorder (PTSD) symptom burden in adult (aged 18-65) survivors of intimate partner violence (IPV).\n\nThis trail will test the following 2 aims:\n\nAIM 1 : To compare the efficacy of a therapeutic psilocybin dose at improving outcomes on the PCL-5 and CAPS-5 as compared to an active control psilocybin dose in IPV survivors with chronic PTSD.\n\nAIM 2: To evaluate the efficacy of psilocybin on quality of life, cognitive function, motor ability, depression, anxiety, and cognitive flexibility.\n\nParticipants will be asked to:\n\n* Complete a 2 part screening process\n* Attend a baseline assessment\n* Complete a psychoeducation preparation session(s)\n* Attend psilocybin administration session (receive high dose \\[25mg\\] or low dose psilocybin \\[1mg\\])\n* Complete 5-6 weekly sessions of ACT\n* Repeat outcome measures at 1-week, 4 weeks, 3 months (online questionnaires only), and 6 months post-psilocybin administration.",[32,28],[118,119,120],"Psychotherapy","Psilocybin","Acceptance and Commitment Therapy","2026-05-11",{"date":123,"type":37},"2026-05-14",{"date":125,"type":20},"2026-08-01",{"date":127,"type":20},"2029-08-01",{"name":129,"class":44},"University of Calgary",{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":135,"acronym":136,"eligibilityCriteria":137,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":138,"targetDuration":4,"studyType":21,"phases":140,"briefSummary":142,"conditions":143,"keywords":146,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":77},"100634944","phase-1-yoga-for-black-and-brown-women-who-have-experienced-abuse-from-an-intimate-partner-100634944","NCT07546266","Yoga for Black and Brown Women Who Have Experienced Abuse From an Intimate Partner","A Culturally Tailored, Trauma-Informed Yoga Program for Women of Color Who Have Experienced Intimate Partner Violence","SOAR","Inclusion Criteria:\n\n* Self-identify as a Woman of Color (WOC).\n* Lifetime experience of intimate partner violence (IPV)\n* Age 18 years or older.\n* Willingness to complete study procedures",{"count":139,"type":20},40,[141],"PHASE1","The goal of this clinical trial is to determine if a culturally tailored and trauma-informed yoga (CT-TIY) program improves the overall well-being of Black and Brown women who have experienced IPV. The main questions it aims to answer are:\n\n* What is the feasibility, acceptability, and safety of delivering the CT-TIY program?\n* Do participants randomized to the CT-TIY program experience increases in our primary outcome of psychological well-being relative to women randomized to an enhanced care-as-usual control condition?\n* Do participants randomized to the CT-TIY program experience improvements in our secondary outcomes of empowerment, resilience, health-related quality of life, collective self-esteem, and culturally specific coping relative to participants randomized to an enhanced care-as-usual control condition? Researchers will compare CT-TIY to enhanced care-as-usual to see if CT-TIY to determine the feasibility, acceptability, safety, as well as initial efficacy of the yoga program.\n\nParticipants randomized to the CT-TIY program will:\n\n* Have 15 weeks to complete a target of 10 CT-TIY yoga classes\n* Provide feedback on the CT-TIY program after each class they attend\n* Complete assessments at Baseline, after completing the CT-TIY program (week 16), as well as 3-months (week 27) after completing the CT-TIY program\n* Complete an exit interview where they provide feedback on their experiences in the yoga program\n\nParticipants randomized to the enhanced care-as-usual control condition will:\n\n* Receive a referral to a domestic violence provider and the Futures without Violence General Health Safety Card, designed to help women recognize how their relationship impacts their health and the lives of their children, and provides information on safety planning and hotlines for support.\n* Complete assessments at Baseline, week 16, and week 27 of the study.",[28,144,145],"Psychological Well Being","Psychological Trauma, Historical",[147,148,149,150,151,94,93],"women of color","minority health","yoga","trauma informed","sister circles","2026-04-22",{"date":154,"type":37},"2026-04-28",{"date":156,"type":20},"2026-05-15",{"date":158,"type":20},"2027-12-31",{"name":160,"class":44},"The University of Akron",{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":166,"acronym":167,"eligibilityCriteria":168,"healthyVolunteers":11,"sex":54,"minAge":169,"maxAge":170,"enrollmentInfo":171,"targetDuration":4,"studyType":21,"phases":173,"briefSummary":174,"conditions":175,"keywords":178,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":182,"lastUpdatePostDateStruct":183,"startDateStruct":185,"completionDateStruct":187,"leadSponsor":188,"locationsCount":77},"100580251","multi-component-family-intervention-to-lower-depression-and-address-intimate-partner-violence-in-nepal-100580251","NCT06834867","Multi-component Family Intervention to Lower Depression and Address Intimate Partner Violence in Nepal","A Randomized Controlled Trial of a Multi-component Family Intervention to Lower Depression and Address Intimate Partner Violence (MILAP) Among Young Women in Nepal","MILAP","Inclusion Criteria:\n\n* Married women aged 15-24 years, their husbands and MILs sharing a household;\n* Living in the catchment area with no stated intention of leaving during the study period;\n* Participants speaking in Maithili or Nepali;\n* Wife reporting Intimate Partner Violence (physical, sexual or abusive control) in last 12 months as measured by three questions from the International Violence Against Women Survey (IVAWS);\n* Expressing desire to remain in the current relationship\u002Ffamily\n\nExclusion Criteria:\n\n* Pregnant women;\n* History of IPV severe enough to result in hospitalization in the past 12 months;\n* Significant cognitive problems\u002Fdisability precluding participation;\n* Any participant with Severe Alcohol Dependence, defined as Severity of Alcohol Dependence Questionnaire (SADQ) \\> 31 (those with mild to moderate dependance will be referred but not excluded)","15 Years","24 Years",{"count":172,"type":20},900,[23],"Intimate Partner Violence (IPV) is a major public health problem in low- and middle-income countries (LMICs). Globally, an estimated 30% of women report physical or sexual violence by an intimate partner in their lifetime. IPV is a well-established social driver of mental health problems, and doubles the rate of depression and post-traumatic stress disorder (PTSD). Interventions like cognitive behavioral therapy (CBT) can improve depression after women experiencing IPV exit abusive relationships. However, despite ongoing violence, many young women in LMICs are less likely to divorce or separate from their husband. But ongoing IPV severely limits mental health recovery and increases the risks of suicide. Another important factor in many LMICs is that young women often live in extended, multi-generational households, where studies have shown that mother-in-laws (MILs) play a critical role in young married women's autonomy and freedom of movement, substantially affecting her mental health. The pathways via which multiple family members and ongoing IPV affect young women's mental health in LMICs is very poorly understood. There is an urgent need to design and assess interventions that: a) improve mental health and reduce IPV; b) engage husbands and MILs, and not just women experiencing IPV; and c) elucidate pathways via which IPV-related drivers affect mental health.\n\nThis study's research team, with over 16 years of experience in Nepal, conducted a pilot study introducing the Multi-component family Intervention to Lower depression and Address intimate Partner violence (MILAP). MILAP, which translates to \"unity and reconciliation\" in Nepali, showed promise in reducing depression and IPV among families (comprising women, husbands, and mothers-in-law). Based on these favorable results, the investigators now propose a 12-month randomized controlled trial (RCT) to assess the effectiveness of MILAP in addressing depression, IPV, and PTSD among young married women in Nepal. The goal of this RCT is to assess the effectiveness of MILAP, understand mechanisms of change for MILAP's effectiveness, and conduct a cost-effectiveness analysis. The specific aims of this study are:\n\nAIM 1: Conduct a 12-month RCT to assess the effectiveness of MILAP on depression, IPV, and PTSD among young married women in Nepal.\n\nAIM 2: Conduct a mixed-methods assessment of theorized mechanisms of change for MILAP's effectiveness.\n\nAIM 3: Conduct a cost-effectiveness analysis of MILAP for depression and IPV.\n\nParticipants of this study will receive either MILAP or enhanced usual care, and will answer questions about depression, IPV and PTSD at baseline, at 1 month and every 3 months until 1-year.",[28,176,177],"Depression","PTSD - Post Traumatic Stress Disorder",[61,176,179,180,181,167],"Family Intervention","Mental Health","Nepal","2026-04-09",{"date":184,"type":37},"2026-04-14",{"date":186,"type":37},"2025-04-04",{"date":74,"type":20},{"name":189,"class":44},"Possible",{"id":191,"slug":192,"hasResults":11,"nctId":193,"briefTitle":194,"officialTitle":194,"acronym":195,"eligibilityCriteria":196,"healthyVolunteers":53,"sex":54,"minAge":197,"maxAge":198,"enrollmentInfo":199,"targetDuration":4,"studyType":21,"phases":201,"briefSummary":202,"conditions":203,"keywords":207,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":211,"lastUpdatePostDateStruct":212,"startDateStruct":213,"completionDateStruct":215,"leadSponsor":217,"locationsCount":77},"100564329","ser-familia-a-family-based-intervention-addressing-syndemic-conditions-among-latino-immigrant-families-100564329","NCT06627764","SER Familia: A Family-Based Intervention Addressing Syndemic Conditions Among Latino Immigrant Families","SER Familia","Inclusion Criteria:\n\n* Eligible participants must identify as Hispanic\u002FLatino\u002Fa\u002Fx\u002Fe,\n* be a first generation immigrant parent or parental figure (Parent)\n* have a child (Youth) aged 12-17\n* speak English and\u002For Spanish\n\nExclusion Criteria:\n\n* Families planning to move within two years will be excluded","12 Years","100 Years",{"count":200,"type":20},400,[23],"This study aims to prevent syndemic health conditions by decreasing acculturative stress and promoting resilience via SER Familia (Salud, Estrés y Resilencia en Familias\u002F Health, Stress, and Resilience in Families), a family-based intervention. SER Familia is a six-session intervention co-developed and delivered by community health workers (CHWs) that uses strategies to reduce acculturative stress, promote resilience, improve parent-child and family level health, while simultaneously helping families maintain strong social networks and better navigate community resources to address social determinants of health (SDOH). More specifically, investigators aim to: 1) Examine the efficacy of SER Familia to prevent or reduce the syndemic comprised of substance abuse, IPV, HIV risk, depression, and anxiety among Parents and Youth; and 2) Identify how individual, family, and community mechanisms of change related to acculturative stress and resilience mediates the effect of SER Familia.",[204,28,205,176,206],"Substance Abuse","HIV Infections","Anxiety",[208,209,210],"Family","Stress","Resilience","2026-04-07",{"date":182,"type":37},{"date":214,"type":37},"2025-06-30",{"date":216,"type":20},"2029-01-31",{"name":218,"class":44},"Duke University",{"id":220,"slug":221,"hasResults":11,"nctId":222,"briefTitle":223,"officialTitle":224,"acronym":225,"eligibilityCriteria":226,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":227,"enrollmentInfo":228,"targetDuration":4,"studyType":21,"phases":230,"briefSummary":231,"conditions":232,"keywords":235,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":237,"lastUpdatePostDateStruct":238,"startDateStruct":240,"completionDateStruct":242,"leadSponsor":244,"locationsCount":77},"100631553","what-works-to-prevent-violence---malawi-moyo-olemekeza-100631553","NCT07502183","What Works to Prevent Violence - Malawi Moyo Olemekeza","What Works to Prevent Violence Against Women and Girls: Impact at Scale: A Cluster Randomized Controlled Trial to Assess the Effectiveness of a Community-mobilisation Intervention to Prevent Violence Against Women in Malawi","WW-M-MO","Inclusion Criteria:\n\n1. The household has a woman aged 18-49 who are in monogamous relationships\n2. The household is food insecure, where food insecurity is scored on a scale of (0-7) and constructed from responses on 3 questions related to the household's food sufficiency (a) How does the household meet its food needs (b) How often does the household has food surplus and (c) How many times do you eat a full meal on a typical day over a year.\n3. The primary decision maker of the household is male\n4. Household is willing to participate in community meetings","49 Years",{"count":229,"type":20},1700,[23],"Violence against women is complex and must be addressed at multiple levels, with leadership from women themselves on how to bring about positive change to free women and girls from daily experiences of violence and to promote their rights. It is in this context that the Pamodzi Kuthetsa Nkhanza (PKN) consortium will implement a programme to facilitate the prevention of intimate partner violence (IPV) in Malawi as one of the most common forms of VAW experienced in Malawi. The programme takes a whole community approach and uses gender transformative approaches at different levels of society to address the root causes of IPV. It will draw primarily on two existing, evidence-based prevention models, namely SASA! Together (community mobilisation model) and Moyo Olemekeza (MO) (gender norms and behaviour change and economic empowerment approach). The institutional strengthening component of these evaluations is meant to create an enabling environment.\n\nThe cRCT described in this protocol will assess the added value of the women's social and economic empowerment programme (MO) when layered on top of SASA! Together for eligible at-risk households.",[28,233,234],"Earning Outcomes","Norms, Social",[61,236],"Economic Empowerment","2026-03-30",{"date":239,"type":37},"2026-04-03",{"date":241,"type":37},"2025-10-15",{"date":243,"type":20},"2029-01",{"name":245,"class":44},"George Washington University",{"id":247,"slug":248,"hasResults":11,"nctId":249,"briefTitle":250,"officialTitle":251,"acronym":4,"eligibilityCriteria":252,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":253,"targetDuration":4,"studyType":21,"phases":255,"briefSummary":256,"conditions":257,"keywords":260,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":265,"lastUpdatePostDateStruct":266,"startDateStruct":268,"completionDateStruct":270,"leadSponsor":272,"locationsCount":4},"100630799","smartphone-climate-adaptation-and-ipv-intervention-for-women-in-informal-settlements-in-kenya-100630799","NCT07492368","Smartphone Climate Adaptation and IPV Intervention for Women in Informal Settlements in Kenya","Development and Testing of a Smartphone-Delivered Climate Adaptation and IPV-Related Stress Intervention for Residents of Informal Settlements in Kenya Using Ecological Momentary Approaches","Inclusion Criteria:\n\n* Female\n* Age 18 years or older\n* Resident of Kibera or Mathare informal settlement in Nairobi, Kenya\n* Speaks Swahili or English\n* Participated in the parent study (1R21MH127356)\n* Reported at least one form of intimate partner violence (psychological, -physical, or sexual) in the past 12 months\n* Willing to provide informed consent\n* Willing to use a smartphone for daily assessments and intervention activities\n\nExclusion Criteria:\n\n* No past-year intimate partner violence reported in parent study\n* Did not participate in the parent study (1R21MH127356)\n* Under 18 years of age\n* Unable to provide informed consent\n* Does not speak Swahili or English\n* Not a resident of Kibera or Mathare informal settlements",{"count":254,"type":20},272,[23],"This study is testing a smartphone-delivered program to help women living in informal settlements in Kenya manage intimate partner violence (IPV) and stress related to extreme weather events. Women in these communities often face high levels of violence from partners, challenges caused by climate-related events, and limited access to support services.\n\nParticipants will be randomly assigned to either a mobile intervention or a comparison condition. The mobile program provides short, tailored sessions that help women learn safety planning, coping skills, and strategies for adapting to climate-related stress. The program also offers tools to improve communication and strengthen social support.\n\nThe main goal of the study is to see whether this smartphone-based approach can reduce the frequency and severity of IPV over 12 months. The study will also examine changes in stress levels, self-confidence in handling problems, social support, and safety behaviors.\n\nResults from this study may help create accessible, scalable support for women experiencing IPV and climate-related stress in similar settings.",[28,258,259],"Climate Change","Stress (Psychology)",[261,262,209,263,264],"Intimate partner violence","Climate","Ecological momentary assessment","Ecological momentary intervention","2026-03-19",{"date":267,"type":37},"2026-03-25",{"date":269,"type":20},"2026-03",{"date":271,"type":20},"2027-07",{"name":273,"class":44},"Africa Institute of Mental and Brain Health (AFRIMEB)",{"id":275,"slug":276,"hasResults":11,"nctId":277,"briefTitle":278,"officialTitle":279,"acronym":280,"eligibilityCriteria":281,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":282,"targetDuration":4,"studyType":21,"phases":284,"briefSummary":285,"conditions":286,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":265,"lastUpdatePostDateStruct":290,"startDateStruct":292,"completionDateStruct":294,"leadSponsor":296,"locationsCount":77},"100570116","a-multi-level-trauma-informed-approach-to-increase-hiv-pre-exposure-prophylaxis-initiation-among-black-women-100570116","NCT06703060","A Multi-Level Trauma-Informed Approach to Increase HIV Pre-exposure Prophylaxis Initiation Among Black Women","Trauma-Informed HIV Prevention for Black Women in Baltimore","MATCH","Inclusion Criteria:\n\n* self-identified Black cisgender woman;\n* self-reported HIV-negative status, and\n* ≥18 years.\n* reports unprotected vaginal or anal sex in the past 6 months with a male sexual partner,\n* have at least one substantial HIV risk factor in the past 6 months according to the 2021 Centers for Disease Control (CDC) PrEP Eligibility Guidelines (i.e., HIV-positive sexual partner, recent bacterial Sexually Transmitted Disease (STD), 2+ sex partners, history of inconsistent or no condom use, commercial sex work, and residing in high HIV prevalence area or network), and\n* never taken PrEP\n\nExclusion Criteria:\n\n* non-English speaking and\n* currently living with HIV",{"count":283,"type":20},300,[23],"U.S. epidemiological data indicates that Black women are a high-risk HIV disparity group, yet initiation of novel prevention strategies like pre-exposure prophylaxis (PrEP) among this group is stagnant. Socio-structural challenges like intimate partner violence and gendered racism can constrain PrEP access among Black women, but few implementation studies have mitigated these challenges to improve PrEP initiation. The proposed research aims to implement and assess the effectiveness, implementation, and sustainability of a multilevel intervention to increase PrEP initiation among Black women with and without intimate partner violence in Baltimore.",[287,288,289,28],"HIV Prevention","PrEP","Women",{"date":291,"type":37},"2026-03-23",{"date":293,"type":37},"2025-02-28",{"date":295,"type":20},"2028-02",{"name":297,"class":44},"Johns Hopkins Bloomberg School of Public Health",{"id":299,"slug":300,"hasResults":11,"nctId":301,"briefTitle":302,"officialTitle":303,"acronym":4,"eligibilityCriteria":304,"healthyVolunteers":53,"sex":54,"minAge":305,"maxAge":4,"enrollmentInfo":306,"targetDuration":4,"studyType":308,"phases":4,"briefSummary":309,"conditions":310,"keywords":314,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":319,"lastUpdatePostDateStruct":320,"startDateStruct":322,"completionDateStruct":324,"leadSponsor":326,"locationsCount":4},"100626378","evaluation-of-a-sexual-violence-and-intimate-partner-violence-primary-prevention-program-implemented-in-drinking-establishments-100626378","NCT07434856","Evaluation of a Sexual Violence and Intimate Partner Violence Primary Prevention Program Implemented in Drinking Establishments","The Safe Night Out Evaluation Study: Evaluation of a Sexual Violence and Intimate Partner Violence Primary Prevention Program Implemented in Drinking Establishments","Inclusion Criteria:\n\n* Aged 21 years or older (as required per California law for alcohol servers)\n* Employed and working as a bar owner, manager, or staff member of the drinking establishment that has been recruited for the study (for staff participants)\n* A customer or patron in the past month at the drinking establishment that has been recruited for the study (for patron participants)\n* Ability to speak and understand English\n\nExclusion Criteria:\n\n* Aged 20 years and under\n* Inability to speak and understand English\n* No current employment at a drinking establishment recruited for the study (for staff participants)\n* No history of visiting the drinking establishment in the past month (for patron participants)","21 Years",{"count":307,"type":20},650,"OBSERVATIONAL","The goal of this project is to evaluate the effectiveness of Safe Night Out, a community-level primary violence prevention program offered in drinking establishments in the Sacramento region of California. The main questions this project aims to answer are: 1) Does the Safe Night Out program reduce incidents of sexual violence and intimate partner violence among patrons? 2) Does the Safe Night Out program increase incidents of safety checks of patrons by staff participants? To address these questions, we will enroll 150 staff participants and 500 patron participants from 25 drinking establishments that have implemented the Safe Night Out program (\\~3 staff participants and 10 patron participants per drinking establishment) and 25 drinking establishments that have not implemented the Safe Night Out program (\\~3 staff participants and 10 patron participants per drinking establishment). Participants will complete a baseline and three 6-month follow-up assessments, until 18 month-follow-up.",[28,311,312,313],"Sexual Violence","Alcohol","Safety",[315,93,316,317,318],"sexual violence","alcohol","bars","clubs","2026-02-19",{"date":321,"type":37},"2026-02-27",{"date":323,"type":20},"2026-06",{"date":325,"type":20},"2028-12",{"name":327,"class":44},"University of California, San Diego",{"id":329,"slug":330,"hasResults":11,"nctId":331,"briefTitle":332,"officialTitle":333,"acronym":334,"eligibilityCriteria":335,"healthyVolunteers":53,"sex":54,"minAge":17,"maxAge":227,"enrollmentInfo":336,"targetDuration":4,"studyType":21,"phases":338,"briefSummary":339,"conditions":340,"keywords":342,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":347,"lastUpdatePostDateStruct":348,"startDateStruct":350,"completionDateStruct":352,"leadSponsor":354,"locationsCount":77},"100576292","what-works---malawi-sasa-together-100576292","NCT06783400","What Works - Malawi SASA! Together","What Works to Prevent Violence Against Women and Girls: Impact at Scale: A Cluster Randomized Controlled Trial to Assess the Effectiveness of a Community-mobilisation Intervention to Prevent Violence Against Women in Malawi - SASA! Together","WW-M-SASA!","Inclusion Criteria:\n\n* Women and men aged 18-49 who have ever been in an intimate (romantic) relationship.\n* Living in selected Group Village Heads (GVHs) in Lilongwe or Balaka districts for at least a year. The specific Traditional Authorities (TAs) in Lilongwe are: Kalolo, Chimutu, Kabudula; The TAs in Balaka are: Msamala and Nyanyala.\n\nExclusion Criteria:\n\n* Women and men younger than 18 years or older than 49 years old\n* Women who have never had an intimate relationship.\n* Not living in selected TAs and GVHs in Lilongwe or Balaka districts, or living in selected GVHs for less than one year\n* Paid employees of the PKN programme (any element), including SASA! Together community activists who deliver the programme activities.",{"count":337,"type":20},4800,[23],"Violence against women is complex and must be addressed at multiple levels, with leadership from women themselves on how to bring about positive change to free women and girls from daily experiences of violence and to promote their rights. It is in this context that the Pamodzi Kuthetsa Nkhanza (PKN) consortium will implement a programme to facilitate the prevention of intimate partner violence (IPV) in Malawi as one of the most common forms of VAW experienced in Malawi. The programme takes a whole community approach and uses gender transformative approaches at different levels of society to address the root causes of IPV. It will draw primarily on two existing, evidence-based prevention models, namely SASA! Together (community mobilisation model) and Moyo Olemekeza (MO) (gender norms and behaviour change and economic empowerment approach).\n\nA cluster randomised controlled trial (cRCT) will evaluate the effectiveness of the PKN programme, assessing the effectiveness of the SASA! Together programme at shifting individual behaviours and reducing violence in intimate relationships while also tackling community norms that drive these forms of violence against women. The cRCT will also assess the added value of combining SASA! Together and a women's social and economic empowerment programme (MO) for most at-risk households.\n\nThis protocol focuses on the evaluation of the SASA! Together programme.",[28,234,341],"Gender Inequitable Behavior",[93,343,344,345,346],"gender","social norms","community mobilization","behavior change","2026-02-10",{"date":349,"type":37},"2026-02-12",{"date":351,"type":37},"2024-08-27",{"date":353,"type":20},"2029-12",{"name":245,"class":44},{"id":356,"slug":357,"hasResults":11,"nctId":358,"briefTitle":359,"officialTitle":359,"acronym":4,"eligibilityCriteria":360,"healthyVolunteers":11,"sex":54,"minAge":17,"maxAge":4,"enrollmentInfo":361,"targetDuration":363,"studyType":308,"phases":4,"briefSummary":364,"conditions":365,"keywords":367,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":369,"lastUpdatePostDateStruct":370,"startDateStruct":372,"completionDateStruct":374,"leadSponsor":376,"locationsCount":77},"100536832","intimate-partner-violence-among-people-who-inject-drugs---prevalence-risk-factors-and-experiences-100536832","NCT06269952","Intimate Partner Violence Among People Who Inject Drugs - Prevalence, Risk Factors and Experiences","Inclusion Criteria: at least 18 years of age, injecting drugs, participating in the needle syringe program in Sweden\n\n\\-\n\nExclusion Criteria:\n\n* under the age of 18\n* heavily intoxicated\n* psychotic symptoms",{"count":362,"type":20},500,"1 Year","There are around 15,6 million people who inject drugs (PWID) worldwide, of which around 3,5 million are women who inject drugs (WWID) (1). In Sweden, estimates suggest 8000-21000 PWID (2). PWID are exposed to substantial health risks that are directly linked to injection drug use, such as blood borne viruses (hepatitis and HIV), overdoses and skin and tissue infections. Additionally psychiatric disorders are common and PWID's general health is often neglected (3,4,5).\n\nIn Sweden, harm reduction units such as needle and syringe programs (NSP) have scaled-up in recent years. In Stockholm the first NSP opened in 2013 and the second in 2018. In 2022, 4600 individuals were enrolled in the program since it opened, of which approximately 25% were women. Around 2000 were active participants, defined as having visited the program at least once during the last 12 months. In 2021 54% of the participants stated amphetamine as the last drug injected, 31% heroin, 4% buprenorphine and 11% other drugs. Most participants were between 30-49 years of age. In addition to distribution of sterile needles and injection paraphernalia, the NSP staff (nurses, doctors, midwifes, counselors) provides services such as testing for blood borne viruses, vaccinations, wound care, take-home naloxone, reproductive health services, counselling, support in contact with social service and referrals for substance use disorder treatment and hepatitis C\u002FHIV treatment.\n\nGender-based violence (GBV) is a global health issue and WHO estimates that one in three women globally have been exposed to some sort of partner violence during their lifespan (7). Intimate partner violence (IPV) is defined as violent behavior between two people who have a close relationship, such as partners, ex-partners, siblings, relatives, friends and alike. In Sweden around 14% of women and 5% of men are exposed to physical violence in an intimate partner relationship during their lifespan however 20-25% of women and around 17% of men are exposed to psychological violence during their lifespan (8; 9). The prevalence of IPV among PWID is estimated to be significantly higher than in the general population (10). A study from USA found the risk of IPV to be three times higher and the prevalence estimated between 35-57% (7). In international studies, IPV exposure is found to be a significant risk factor for needle sharing among WWID (11, 12). There are other well-known consequences of IPV including impact on sexual and reproductive health rights, physical and psychological wellbeing, increased risk of contracting HIV and hepatitis C (13; 14). IPV exposure disproportionately affects WWID worldwide, however studies in Sweden on IPV exposure in the PWID population is scarce. To date there are studies that address this among women with substance use disorders but none with an exclusive focus on PWID or WWID. In clinical research of women diagnosed with substance use disorders (SUD) with psychiatric comorbidities and social challenges, one study indicates that the majority (91%, n=79) of women had been exposed to some form of IPV (15). Another study of women with SUD (n=52), 50% reported exposure of serious violence and the majority (96%) reported exposure to psychological violence (10). There are different types of IPV; psychological, physical, sexual, financial, latent, digital, neglect, honor related, aftermath of IPV (16). Our research team has previously carried out a qualitative interview study among WWID at the Stockholm NSP in 2019 to investigate reasons and barriers for participation among women (17). The interviews illustrated that IPV is common. In the proposed studies, for this doctoral thesis, we have chosen to focus on physical, sexual, psychological and financial violence among PWID motivated by findings in our previous research.\n\nPWID and specifically WWID are regarded as groups who are especially vulnerable for IPV exposure and should therefore be prioritized in the national efforts to prevent IPV (15). However, there are no studies estimating the prevalence and frequency of IPV among PWID in Sweden. Previous international studies suggest that PWID are exposed to IPV to a greater extent than the general population, and women with substance use disorders are exposed to an alarming degree of violence (15). In Sweden there are no tailored interventions for PWID or WWID who are exposed to IPV, it is reasonable to believe that there is a need for a multi-faceted program for PWID exposed to IPV, however this is still unexplored.\n\nThe overall aim of this project is to increase knowledge about IPV among PWID and WWID as particularly vulnerable groups in regards to IPV. More specifically, the aim is to investigate the prevalence and frequency of different types of IPV among PWID at the Stockholm NSP and to explore the experiences' of IPV, needs and preferences for IPV support among WWID to facilitate tailored support and prevention programs for those exposed.",[28,366],"People Who Inject Drugs",[93,94,368],"people who inject drugs","2026-02-02",{"date":371,"type":37},"2026-02-05",{"date":373,"type":37},"2023-10-05",{"date":375,"type":20},"2026-07",{"name":377,"class":378},"Region Stockholm","OTHER_GOV",{"id":380,"slug":381,"hasResults":11,"nctId":382,"briefTitle":383,"officialTitle":383,"acronym":4,"eligibilityCriteria":384,"healthyVolunteers":53,"sex":54,"minAge":305,"maxAge":110,"enrollmentInfo":385,"targetDuration":4,"studyType":21,"phases":387,"briefSummary":388,"conditions":389,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":392,"lastUpdatePostDateStruct":393,"startDateStruct":395,"completionDateStruct":397,"leadSponsor":398,"locationsCount":77},"100582635","alcohol-and-sexual-communication-among-couples-in-the-laboratory-100582635","NCT06865872","Alcohol and Sexual Communication Among Couples in the Laboratory","Inclusion Criteria:\n\n1. Provision of signed and dated informed consent form.\n2. Stated willingness to comply with all study procedures and lifestyle considerations.\n3. Both partners must identify as cisgender via self-report on the Baseline Questionnaire.\n4. At least one partner within the couple must be a man via self-report on the Baseline Questionnaire.\n5. Both partners must be between 21 and 65 years old, verified by a photo ID.\n6. In an intimate relationship lasting at least one month in which they engaged in sexual activity at least once in the past month with their partner via self-report on the Baseline Questionnaire.\n7. Both partners must report that they consumed a weight-based amount of alcohol that is equal to or greater than the dose to be administered in the lab at least three times during the past year via self-report on question #5 of the NIAAA Alcohol Consumption Measure.\n\nPlease contact clinical site for additional inclusion criteria.\n\nExclusion Criteria:\n\n1. Treatment for Alcohol or Drug Use: currently being treated for alcohol, or drug problems; currently interested in seeking treatment for drinking or drug use via self-report.\n2. Any medical or psychiatric condition, as well as current use of a medication, that would contraindicate alcohol administration via self-report:\n\n   * Cardiac Pacemaker\n   * Asthma: emergency room visit related to asthma in the past year; use of inhaler more frequently when drinking alcohol; use of oral steroid treatments for asthma in the past year\n   * Head Injury: any past serious head injuries\n   * Acute Psychiatric Symptomatology: elevated psychological distress as indicated by a score greater than 65 on the Brief Symptom Inventory\n3. Self-report that a participant is trying to get pregnant, currently pregnant, or currently breastfeeding or a positive pregnancy test.\n4. Combined height and weight that is either less than 6 feet tall and over 230 lbs, or over 250 lbs and over 6 ft tall as measured during the lab visit.\n\nPlease contact clinical site for additional exclusion criteria.",{"count":386,"type":20},480,[23],"Intimate Partner Sexual Violence (IPSV) is a significant and understudied public health problem among couples, yet little is known about factors that contribute to IPSV perpetration. This proposal aims to determine the acute effect of alcohol and sexual communication on IPSV. In this study, 240 couples who drink alcohol will be recruited from the Metro-Denver area. Upon arrival to the laboratory, a trained research assistant will check the participant's ID, verify that they adhered to the pre-session guidelines, administer a breath test to ensure a breath alcohol content (BrAC) of 0.00 and conduct a field sobriety test. They will also obtain informed consent for each member of the couple separately. Female participants will take a pregnancy test to ensure a negative result. All participants will complete measures to reverify eligibility criteria and be weighed to determine their correct alcohol dose. Partners will separately complete a baseline survey measuring demographic factors, alcohol use, sexual communication, and daily experiences. After completing the survey, participants will be assigned a beverage condition (alcohol or no-alcohol control) and couples will be randomly assigned to a communication condition (direct verbal or indirect verbal). Participants will be seated in a room separate from their partner, where they will drink an alcoholic or no-alcohol control beverage. Upon reaching a breath alcohol content (BrAC) of .07, or immediately after drinking in the No-Alcohol control condition, participants will complete a laboratory assessment of sexual violence. The main hypotheses are: (1) one's alcohol use will increase IPSV toward partners who are also drinking, (2) one's alcohol use will increase IPSV among partners who use indirect, relative to direct, communication, and (3) actor alcohol use will increase IPSV toward partners who are also drinking and use indirect, relative to direct, communication.",[390,28,391],"Alcohol Intoxication","Communication","2025-10-24",{"date":394,"type":37},"2025-10-28",{"date":396,"type":37},"2025-04-18",{"date":295,"type":20},{"name":399,"class":44},"University of Colorado, Denver",{"id":401,"slug":402,"hasResults":11,"nctId":403,"briefTitle":404,"officialTitle":405,"acronym":406,"eligibilityCriteria":407,"healthyVolunteers":53,"sex":54,"minAge":17,"maxAge":4,"enrollmentInfo":408,"targetDuration":4,"studyType":21,"phases":410,"briefSummary":411,"conditions":412,"keywords":419,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":241,"lastUpdatePostDateStruct":428,"startDateStruct":430,"completionDateStruct":432,"leadSponsor":434,"locationsCount":77},"100600344","get-better-together-relationship-education-for-military-couples-100600344","NCT07096271","Get Better Together: Relationship Education For Military Couples","Better Together: A Relationship Enrichment Program Targeting Transdiagnostic Interpersonal Emotion Regulation Among Military Couples","GBT RCT","Inclusion Criteria:\n\n* Couple is in a committed romantic relationship of at least six months\n* At least one partner is a military Service member on active duty\n* Both partners are age 18 or older\n* Couple has not previously attended a relationship enrichment retreat or workshop together (e.g., CREDO, Strong Bonds, BSRT). This does not include couples therapy or pre-marital counseling.\n\nExclusion Criteria:\n\n* One or both partners decline to provide informed consent\n* Required command endorsement for retreat attendance is not received (for Service members E-6 and below)\n* Couple is unable or unwilling to attend any of the scheduled retreats during the study period",{"count":409,"type":20},1000,[23],"This study is testing a program called Get Better Together, a relationship education program designed to help military couples effectively navigate life stressors as a team. The goal is to find out if attending Get Better Together improves mental health and relationship skills, and reduces problems like alcohol misuse, aggression, and suicide risk. Couples who join the study will be randomly placed into one of two groups. One group will attend Get Better Together at a weekend retreat. The other group will continue their usual activities and later receive access to an online relationship education program. All participants will complete surveys before the retreat and again 2, 4, and 6 months later.",[413,414,415,416,28,417,418],"Emotion Regulation","Relationship Conflict","Suicide Risk","Alcohol Use","Relationship Distress","Interpersonal Emotion Regulation",[420,421,422,423,424,425,426,427],"Behavioral: Get Better Together (GBT)","military","intimate relationships","suicide prevention","primary prevention","emotion regulation","relationship education","interpersonal emotion regulation",{"date":429,"type":37},"2025-10-20",{"date":431,"type":37},"2025-09-22",{"date":433,"type":20},"2028-07",{"name":435,"class":44},"Henry M. Jackson Foundation for the Advancement of Military Medicine",{"id":437,"slug":438,"hasResults":11,"nctId":439,"briefTitle":440,"officialTitle":441,"acronym":442,"eligibilityCriteria":443,"healthyVolunteers":11,"sex":54,"minAge":17,"maxAge":4,"enrollmentInfo":444,"targetDuration":4,"studyType":21,"phases":446,"briefSummary":447,"conditions":448,"keywords":449,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":454,"lastUpdatePostDateStruct":455,"startDateStruct":457,"completionDateStruct":459,"leadSponsor":461,"locationsCount":102},"100585740","rise-versus-advocacy-based-enhanced-care-as-usual-for-patients-experiencing-ipv-100585740","NCT06906302","RISE Versus Advocacy-based Enhanced Care as Usual for Patients Experiencing IPV","Recovering From IPV Through Strengths and Empowerment (RISE) Versus Advocacy-based Enhanced Care as Usual for Patients Experiencing IPV","RISE","Inclusion Criteria:\n\n* patients receiving care at an enrolled site\u002Faffiliated Community-Based Outpatient Clinic (CBOC)\n* report experience of past-year physical, psychological, and\u002For sexual IPV on an established screening tool used to detect IPV in VHA, and\n* be able to provide informed consent including permission to have intervention sessions recorded\n\nExclusion Criteria:\n\n* severe cognitive impairment,\n* suicide or homicide intent with a specific plan\n* untreated or unstable symptoms of mania or psychosis",{"count":445,"type":20},172,[23],"This study aims to improve treatment for Veterans Health Administration (VHA) patients who experience intimate partner violence (IPV). This study will evaluate two brief counseling interventions for VHA patients who have experienced IPV in the past 12 months: Recovering from IPV through Strength and Empowerment (RISE) and advocacy-based Enhanced Care as Usual (ECAU). The RISE intervention includes up to 8 sessions and includes specific topic areas (e.g., social support, health effects, resources). The other intervention, ECAU, includes a single session that includes supportive education about IPV and health effects, discussion of ways to increase safety, and information about resources. This study will test which approach is better for improving self-efficacy and other aspects of health.\n\nParticipants will answer surveys about their self-efficacy and other health and safety indicators (e.g., mental health symptoms) right before receiving treatment, approximately 12 weeks later, and then every three months after that for one year. Participation in this research will last about 15 months.",[28],[442,450,451,452,176,453],"Enhanced Care as Usual (ECAU)","Healthcare patients","Self-efficacy","Post-Traumatic Stress Disorders (PTSD)","2025-10-09",{"date":456,"type":37},"2025-10-14",{"date":458,"type":37},"2025-09-15",{"date":460,"type":20},"2030-01",{"name":462,"class":44},"Boston University",{"id":464,"slug":465,"hasResults":11,"nctId":466,"briefTitle":467,"officialTitle":467,"acronym":468,"eligibilityCriteria":469,"healthyVolunteers":53,"sex":54,"minAge":17,"maxAge":470,"enrollmentInfo":471,"targetDuration":4,"studyType":21,"phases":473,"briefSummary":474,"conditions":475,"keywords":480,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":485,"lastUpdatePostDateStruct":486,"startDateStruct":488,"completionDateStruct":490,"leadSponsor":491,"locationsCount":77},"100587883","phase-2-cultural-adaptation-of-a-web-based-app-myplan-thailand-to-empower-and-support-friends-and-family-of-intimate-partner-violence-survivors-100587883","NCT06934174","Cultural Adaptation of a Web-Based App (myPlan Thailand) to Empower and Support Friends and Family of Intimate Partner Violence Survivors","IPV","Inclusion Criteria:\n\n* being female or males who have a female friend currently (past 6 months) experiencing IPV\n* Thai speaking\u002Freading\n* At least 18 years old\n* Have access to a safe smart-phone or computer with internet\n* Have safe email address\n* Living in Thailand\n\nExclusion Criteria:\n\n* Cannot speak\u002Freading Thai\n* Less than age 18 years old\n* Cannot access to a safe smartphone or computer with internet\n* Not living in Thailand","60 Years",{"count":472,"type":20},100,[114],"This research will support and empower friends\u002Ffamily (F\u002FF) of intimate partner violence (IPV) survivors in Thailand, where IPV is critical and common, and survivors first and foremost seek help for abuse from their F\u002FF. myPlan app (www.myPlanapp.org) is a free mobile evidence-based intervention app to prevent IPV. The app was first developed in the United States (US) and has been disseminated to high-income countries (e.g., New Zealand, Canada, Australia) and lowincome (Kenya). One new hope for improving survivors' psychological and well-being is adapting and introducing the myPlan app for the concerned friends\u002Ffamily who support survivors in Thailand.\n\nTherefore, the propose of this longitudinal research study, Cultural Adaptation of a Web-Based App (myPlan Thailand) to Empower and Support Friends\u002FFamily of Intimate Partner Violence Survivors in Thailand, will have two consecutive phases with three aims: 1) To tailor the myPlan app content for concerned F\u002FF members of Thai IPV survivors, 2) To integrate the adapted myPlan app content for concerned F\u002FF members of Thai IPV survivors, 3) To test the feasibility and acceptability of the adapted myPlan app with concerned F\u002FF members of Thai IPV survivors. Phase 1 (Year 1-2) will achieve aim 1-2 to tailor the myPlan app with Thai survivors and friends\u002Ffamily. The investigators will review current content and conduct in-depth interviews with survivors and concerned F\u002FF members on social norms associated with IPV, informal support systems and the role\u002Fresponsibility in helping survivors, safety strategies used by concerned F\u002FF members and negative consequences for both survivor and F\u002FF member providing support. Moreover, in phase 1, the adapted content will be pilot tested with concerned F\u002FF members of survivors by using cognitive techniques and theater-testing methodology.\n\nPhase 2 (Year 3-4) will achieve aim 3 to test the feasibility and acceptability of the adapted myPlan app with F\u002FF. The investigators will conduct a two-group RCT design with concerned F\u002FF member randomized to receive a) the myPlan app for F\u002FF member, or b) standard usual-care safety planning information. Primary outcomes for F\u002FF members include change in knowledge and attitudes towards IPV and F\u002FF empowerment to plan and take safety support survivor. Secondary outcomes will examine change in F\u002FF' distress, frustration and consequences for supporting the survivor. This phase will also collect feasibility and acceptability data to informed a planned R01 submission in Year 3 of the study. The K43 application outlines a four-year plan to support a candidate who is a nursing instructor with 15 years of work in diverse projects, settings, and disciplines; which positions her for a successful career as an independent researcher in research field of intimate partner violence. The career development plan provides a sequence of carefully selected training and mentoring experiences, including coursework to increase research capacity, leadership skills, mentored research leading to a R01 proposal, peer reviewed publications, and professional networking, that will catapult this research to the next level of research achievement. The team will be a collaboration between the Boromarajonani College of Nursing Khon Kaen (BCNKK), Khon Kaen One Stop Crisis Center (OSCC), Johns Hopkins University (JHU), Notre Dame of Maryland University (NDM), and Auckland University of Technology (AUT), New Zealand.",[28,476,477,478,479],"Social Support","Empowerment","mHealth","Effectiveness",[261,481,313,482,483,484],"Friends\u002FFamily memeber","Social support","mHealth intervention","Thailand","2025-05-08",{"date":487,"type":37},"2025-05-13",{"date":489,"type":37},"2025-04-17",{"date":323,"type":20},{"name":492,"class":44},"Boromarajonani College of Nursing, Khon Kaen",{"id":494,"slug":495,"hasResults":11,"nctId":496,"briefTitle":497,"officialTitle":498,"acronym":4,"eligibilityCriteria":499,"healthyVolunteers":53,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":500,"targetDuration":4,"studyType":21,"phases":501,"briefSummary":502,"conditions":503,"keywords":506,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":508,"lastUpdatePostDateStruct":509,"startDateStruct":511,"completionDateStruct":513,"leadSponsor":515,"locationsCount":77},"100568903","effectiveness-of-interpersonal-relationship-psychotherapy-intervention-for-female-victims-of-intimate-partner-violence-100568903","NCT06687278","Effectiveness of Interpersonal Relationship Psychotherapy Intervention for Female Victims of Intimate Partner Violence","The Effect of Interpersonal Relationship Psychotherapy-Based Intervention Program on Psychosocial Well-Being of Female Victims of Intimate Partner Violence","Inclusion Criteria:\n\n* Proficiency in the Turkish language, including the ability to speak and understand it.\n* Exposure to any form of violence perpetrated by an intimate partner.\n\nExclusion Criteria:\n\n* Exposure to violence by an individual other than an intimate partner for the purpose of maintaining group homogeneity.\n* Presence of sensory loss, including but not limited to hearing and vision.\n* Physical injury and\u002For disability resulting from violence that precludes participation in the intervention program.\n* Diagnosis of schizophrenia spectrum disorders and other psychotic disorders.\n* Presence of active self-destructive thoughts and\u002For plans.",{"count":139,"type":20},[23],"This interventional study aims to examine the impact of the Interpersonal Relationship Psychotherapy-Based Intervention Program on the psychosocial well-being of female victims of intimate partner violence.\n\nThe main questions to be answered are the following:\n\n1. Is the Interpersonal Relationship Psychotherapy-Based Intervention Program effective on the interpersonal problems of female victims of intimate partner violence?\n2. Is the Interpersonal Relationship Psychotherapy-Based Intervention Program effective on the mental well-being of female victims of intimate partner violence?\n\nThe study will include eight individual interviews using a variety of data collection forms.",[28,504,505],"Interpersonal Psychotherapy","Interpersonal Relations",[61,507,505,504,180],"Psychological Well-Being","2025-04-25",{"date":510,"type":37},"2025-04-29",{"date":512,"type":37},"2025-02-03",{"date":514,"type":20},"2025-06",{"name":516,"class":44},"Istanbul University - Cerrahpasa",{"id":518,"slug":519,"hasResults":11,"nctId":520,"briefTitle":521,"officialTitle":521,"acronym":522,"eligibilityCriteria":523,"healthyVolunteers":53,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":524,"targetDuration":4,"studyType":21,"phases":525,"briefSummary":526,"conditions":527,"keywords":530,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":532,"lastUpdatePostDateStruct":533,"startDateStruct":535,"completionDateStruct":537,"leadSponsor":539,"locationsCount":4},"100580496","the-effect-of-laughter-yoga-supported-strong-woman-safe-life-training-program-on-attitudes-towards-violence-styles-of-coping-with-stress-and-psychological-flexibility-100580496","NCT06838052","The Effect of Laughter Yoga-Supported Strong Woman, Safe Life Training Program on Attitudes Towards Violence, Styles of Coping with Stress and Psychological Flexibility","Laughter Yoga","Inclusion Criteria Being a woman Being 18 years of age or older Having a partner, speaking, understanding Reading and writing in Turkish Being registered in a women's education and culture center\n\nExclusion Criteria Having any communication barrier Having a diagnosed psychiatric illness Having attended a planned training on violence",{"count":77,"type":20},[23],"The aim of this project is to examine the effects of the Laughter Yoga Supported Strong Woman, Safe Life Education Program applied to women on attitudes towards violence, stress coping styles and psychological flexibility.\n\nThe problem of violence against women is a public health problem that affects and concerns not only women at the individual level, but also children, all family members and therefore society. According to the data of the Turkish Statistical Institute in our country, 38% of women have been subjected to spousal or partner violence at some point in their lives. Violence or the threat of violence that causes fear, pain and anxiety in women from an individual perspective; constitutes an obstacle to women's more active and productive participation in economic and social life, especially in the private sphere. From a social perspective, the economic cost of violence against women is extremely high in terms of loss of working hours and wages, social services, legal and medical expenses.\n\nOur country has a culturally patriarchal social structure. Living in a patriarchal order affects beliefs and attitudes towards the acceptance of violence, making women more vulnerable to violence. Living in a patriarchal order affects beliefs and attitudes towards acceptance of violence, making women more vulnerable to violence. When the reasons for submissive behaviors towards violence are examined, it is stated that factors such as having children, low self-esteem, religious beliefs, social pressure, emotional attachment to a long-term relationship, running away from home, arranged marriage, being economically dependent on the spouse and low level of education are effective. Accepting violence encourages aggression and causes violent people to legitimize their actions. It is stated that submissive and accepting attitudes towards violence can be changed. Interventions aimed at empowering women play an important role in reducing attitudes accepting violence. It is anticipated that this project will create an opportunity for women to raise awareness about violence and change their accepting attitudes towards violence.\n\nThe proposed project consists of THREE stages. The first stage, PREPARATION stage; includes preparation of data collection tools, determination and informing of scholarship recipients, development of training content and tools, preliminary application and determination of the working group. The second stage is the IMPLEMENTATION stage, which includes collecting pre-test data, loading public transportation fees onto participants' cards for transportation, providing training to the intervention group, and collecting post-test data. The third stage is the MONITORING-EVALUATION stage, which is the stage of collecting follow-up test data and conducting analyses.\n\nThe research will be conducted as a randomized controlled parallel group intervention study. The universe of the research will consist of 7988 women registered in 24 Women's Education and Culture Centers (KEKM) affiliated with Altındağ Municipality. 1 center will be randomly selected from 24 Women's Education and Culture Centers for the sample of the research. In this study, the smallest sample size was determined as 43 for each group, totaling 86, at 80% statistical power and α=.05 significance level. Considering the 10% data loss in the determined sample size, it was planned to include a total of 94 participants, 47 for each group. The assignment of the women included in the research to the intervention (47 participants) and control (47 participants) groups will be done by randomization method. The aim is to implement the Laughter Yoga Supported Strong Woman, Safe Life Training Program face-to-face for an 8-week period for the participants in the intervention group. The 47 participants in the intervention group will be divided into 3 separate groups (16 participants, 16 participants and 15 participants) to increase interaction and experience sharing. The project team will implement the Laughter Yoga Supported Strong Woman, Safe Life Training Program consisting of 8 modules to 3 separate groups. The intervention group will be given a pre-test before the training, a post-test after the training and a follow-up test 1 month after the training is completed. It is planned to collect data by conducting a pre-test, post-test and follow-up test simultaneously with the experimental group without any intervention for the control group. Data will be collected using the Attitude Towards Violence in Close Relationships Scale, the Psychological Flexibility Scale and the Styles of Coping with Stress Scale. Institutional permission will be obtained from the Ankara University Ethics Committee and the Altındağ Municipality.\n\nIn this project, with the \"Strong Woman, Safe Life Training Program Supported by Laughter Yoga\", women will be provided with training on the Importance of Self-Knowledge and Communication, Stress and Coping Techniques, Gender, Empowerment",[528,522,28,529,210],"Violence Against Women (VAW)","Coping Skills",[531],"Woman, Married Persons, Laughter Yoga, Intimate partner violence, Stress,Coping Skills, Elasticity, Psychological, Resilience","2025-02-18",{"date":534,"type":37},"2025-02-20",{"date":536,"type":20},"2025-09-20",{"date":538,"type":20},"2026-12-20",{"name":540,"class":44},"Ankara University"]