[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"domestic-violence\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:domestic-violence":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,45,74,102,138,163,184],{"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":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"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":5,"type":19},"ESTIMATED","INTERVENTIONAL",[22],"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",[25,26,27,28,29,30,31],"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":35,"type":36},"2026-06-24","ACTUAL",{"date":38,"type":19},"2026-06-15",{"date":40,"type":19},"2027-08-31",{"name":42,"class":43},"Dawn A. Goddard-Eckrich","OTHER",2,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":20,"phases":55,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":73},"100605695","clinical-trial-to-reduce-perinatal-intimate-partner-violence-100605695","NCT07165860","Clinical Trial to Reduce Perinatal Intimate Partner Violence","Novel Doula Intervention to Leverage Clinic-community Connections to Support Perinatal Intimate Partner Violence Survivors","Inclusion Criteria: Perinatal IPV survivors are eligible if they:\n\n* 1\\) feel comfortable completing the study in Spanish or English\n* 2\\) are age 18 or older\n* 3\\) are no more than 24 weeks 6 days gestation (note: participants enrolled earliest at 18 weeks, baseline at 22 weeks with a 3 week window)\n* 4\\) identify as an IPV survivor by answering affirmatively to a definition of experiencing IPV\n* 5\\) live within a 50 mile radius of Pittsburgh, Pennsylvania\n* 6\\) able to provide safe and complete contact information or take a study cell phone\n\nExclusion Criteria:\n\n* Unable to consent\n* Do not meet inclusion criteria\n* Cannot provide safe contact information or take a study cell phone\n* Incarcerated",true,{"count":54,"type":19},250,[22],"This is a two-armed, fully powered hybrid type 1 trial to test the effectiveness of a doula intervention compared with an active control in reducing intimate partner violence (IPV) among perinatal IPV survivors",[29,58],"Perinatal Problems",[60,61,62],"intimate partner violence","perinatal health","doula","RECRUITING","2026-04-13",{"date":66,"type":36},"2026-04-16",{"date":68,"type":36},"2025-11-01",{"date":70,"type":19},"2029-05-01",{"name":72,"class":43},"University of Pittsburgh",3,{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":52,"sex":16,"minAge":17,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":20,"phases":85,"briefSummary":86,"conditions":87,"keywords":89,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":101},"100624122","camouflaged-wechat-based-intervention-for-abused-women-100624122","NCT07405528","Camouflaged WeChat-based Intervention for Abused Women","Camouflaged WeChat Mini-program-based Intervention for Women Victims of Intimate Partner Violence: Protocol for a Pilot Mixed Methods Study","IPV","Inclusion Criteria:\n\n1. Chinese-speaking (Mandarin or Cantonese)\n2. women aged 18 to 45 years\n3. originally from mainland China and have moved to Hong Kong for at least one year\n4. screened positive for IPV during heterosexual relationships in the past year\n5. have a smartphone with WeChat installed\n6. with no plans to move outside Hong Kong in the next one year\n\nExclusion Criteria:\n\n1. unwilling to provide informed consent\n2. severe chronic diseases (e.g., cancer, heart failure, kidney failure, chronic obstructive pulmonary disease, and HIV\u002FAIDS)\n3. currently experience severe IPV (identified using the revised 11-item Danger Assessment)","45 Years",{"count":84,"type":19},86,[22],"Intimate partner violence (IPV) is a major public health issue and human rights threat worldwide, especially for Chinese immigrant women victims in Hong Kong. Interventions that address negative physical and emotional outcomes from IPV could therefore play a crucial role in enhancing empowerment, social support, and healthy lifestyle among these women. The overall objective of this pilot mixed methods study is to determine the feasibility and acceptability of a camouflaged WeChat mini-program-based WOMEN Health intervention for women victims of IPV. This study will evaluate the feasibility and acceptability of a camouflaged WeChat mini-program-based WOMEN Health intervention for women victims of IPV.",[29,88],"Mental Health Wellness 1",[29,90,91],"Intimate partner violence","mHealth intervention","2026-02-04",{"date":94,"type":36},"2026-02-12",{"date":96,"type":19},"2026-02",{"date":98,"type":19},"2027-02",{"name":100,"class":43},"The University of Hong Kong",1,{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":109,"minAge":110,"maxAge":4,"enrollmentInfo":111,"targetDuration":4,"studyType":20,"phases":113,"briefSummary":114,"conditions":115,"keywords":124,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":101},"100616284","improving-outcomes-in-social-services-through-routine-outcome-monitoring-and-systematic-client-feedback-100616284","NCT07303608","Improving Outcomes in Social Services Through Routine Outcome Monitoring and Systematic Client Feedback","Empowering Clients, Preventing Dropout and Improving Outcomes Through Routine Outcome Monitoring and Systematic Client Feedback in Social Services","Inclusion Criteria:\n\nPeople who have been granted assistance under the Social Services Act at includes centers.\n\nExclusion Criteria:\n\n* People who do not have sufficient knowledge of Swedish or have impaired cognitive functions that prevent them from using FIT in Swedish, as they cannot benefit from the intervention that the study intends to evaluate the effects of. This is assessed by the respective social service.\n* People who receive support and treatment interventions that are not voluntary, i.e. interventions according to the Act on the Compulsory Care of Young People (LVU) or the Act on the Compulsory Care of Drug Abusers (LVM)","ALL","15 Years",{"count":112,"type":19},400,[22],"In this project the investigators want to test whether a new method FIT (Feedback informed treatment) can improve the interventions people receive through social services. The FIT method involves regularly providing information about how the client think things are going and what the client thinks about the help and care they receive.",[116,117,29,118,119,120,121,122,123],"Substance Use Disorders","Criminal Behavior","Social Care","Family Communication","Family Conflict","Child Behavior Problem","Housing","Everyday Activities",[125,126,127,128],"Social services","Feedback informed treatment","Systematic client feedback","Routine outcome management","2025-12-18",{"date":131,"type":36},"2025-12-26",{"date":133,"type":36},"2025-12-05",{"date":135,"type":19},"2028-12-15",{"name":137,"class":43},"Karolinska Institutet",{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":143,"acronym":80,"eligibilityCriteria":144,"healthyVolunteers":11,"sex":109,"minAge":17,"maxAge":145,"enrollmentInfo":146,"targetDuration":4,"studyType":20,"phases":148,"briefSummary":149,"conditions":150,"keywords":151,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":101},"100578248","occupational-therapy-for-adults-who-have-experienced-intimate-partner-violence-ipv-100578248","NCT06808828","Occupational Therapy for Adults Who Have Experienced Intimate Partner Violence (IPV)","Occupational Therapy for Adults Who Have Experienced Intimate Partner Violence","Inclusion Criteria:\n\n* Male or Female 18 years of age or older receiving services from a domestic violence organization\n\nExclusion Criteria:\n\n* None","70 Years",{"count":147,"type":19},25,[22],"The purpose of this graduate student research study is to understand the effectiveness of an occupational therapy program in a domestic violence shelter. It is expected that participation will last about 6 weeks. Subjects will complete pretests involving lifestyle assessments and a coping scale and then participate in 8 occupational therapy sessions during the 4 weeks of program implementation. The occupational therapy sessions will last approximately 90 minutes. After the program is completed, subjects will complete the posttests.\n\nProcedures and Activities. You will be asked to:\n\nComplete a series of questionnaires about your health, well-being, and daily activities.\n\nParticipate in 8 OT sessions that may include activities such as journaling, positive self-talk, coping skills methods, and grounding exercises.\n\nComplete the posttests.",[29],[152,60,153],"domestic violence","occupational therapy","2025-07-23",{"date":156,"type":36},"2025-07-25",{"date":158,"type":36},"2025-02-03",{"date":160,"type":19},"2026-09",{"name":162,"class":43},"Loma Linda University",{"id":164,"slug":165,"hasResults":11,"nctId":166,"briefTitle":167,"officialTitle":167,"acronym":168,"eligibilityCriteria":169,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":170,"targetDuration":4,"studyType":172,"phases":4,"briefSummary":173,"conditions":174,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":175,"lastUpdatePostDateStruct":176,"startDateStruct":178,"completionDateStruct":180,"leadSponsor":182,"locationsCount":44},"100594135","self-dehumanization-and-hesitation-to-report-domestic-violence-100594135","NCT07015502","Self-Dehumanization and Hesitation to Report Domestic Violence","DESHUMA","Inclusion Criteria:\n\n* Woman over 18\n* Victim of physical and\u002For psychological domestic violence taken into care for this reason, following an initial complaint\n* Understanding and speaking French\n* Subject affiliated to a social security scheme\n\nExclusion Criteria:\n\n* Patient under legal protection measure (guardianship or legal protection)\n* Presence of a disabling mental or cognitive disorder\n* Patient employed by the investigator",{"count":171,"type":19},84,"OBSERVATIONAL","The patients included in the study will be adult women who are victims of domestic violence, consulting for this reason. The duration of participation of each patient will be one hour.\n\nAfter obtaining the patient's non-opposition to her participation in the study, socio-demographic and history of violence suffered will be collected during an interview with the doctor\u002Fnurse. After that, the hetero-questionnaire MADRS (Montgomery-Asberg Depression Rating Scale) will be administered to the patient. This first part will last 30 minutes.\n\nThe second part of the study, carried out immediately after the interview, will be carried out on computer in the form of 4 self-questionnaires (Childhood Trauma Questionnaire, Deshumanization Measure within Romantic Relationships scale, self-esteem scale, violentometer) and an implicit association test (IAT). This second part will last 30 minutes.\n\nThen, the participation of the patient in the study is over.",[29],"2025-06-03",{"date":177,"type":36},"2025-06-11",{"date":179,"type":36},"2024-12-20",{"date":181,"type":19},"2025-12-19",{"name":183,"class":43},"Centre Hospitalier Henri Laborit",{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":190,"eligibilityCriteria":191,"healthyVolunteers":52,"sex":109,"minAge":4,"maxAge":4,"enrollmentInfo":192,"targetDuration":4,"studyType":20,"phases":194,"briefSummary":195,"conditions":196,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":200,"lastUpdatePostDateStruct":201,"startDateStruct":203,"completionDateStruct":205,"leadSponsor":207,"locationsCount":101},"100428341","adaptation-and-pilot-testing-of-web-and-mobile-interface-for-the-attach-intervention-100428341","NCT04857775","Adaptation and Pilot Testing of Web and Mobile Interface for the ATTACH™ Intervention","Attachment and Child Health (ATTACH™)","ATTACH™","Inclusion Criteria:\n\n* parents with children between birth and 32 months of age (based on selection of age-appropriate tools for assessing children's health and development)\n* parents agree to participate in the ATTACH™ program consisting of 10-12 weeks of one-hour per week parent training sessions\n* parents agreed to bring a co-parent for 2-3 of the 10 sessions (when possible)\n* parents agree to the dried blood sample collection from themselves and their children (in Calgary agencies)\n\nExclusion Criteria:\n\n\\-",{"count":193,"type":19},100,[22],"COVID-19 has placed unprecedented strains on parents impacted by toxic stressors (depression, addiction, family violence, and poverty) and reluctant to see mental health-service providers in home\u002Fclinic due to fears of infection. Due to the pandemic, PI Letourneau ceased\u002Fdelayed recruitment in ATTACH™, a CIHR-funded randomized controlled trials (RCT) of in-person (home or clinic) program designed to improve children's mental, emotional and behavioral (MEB) health and development via parent-child relationship intervention. Recognizing the heightened need for already vulnerable families to obtain safe parenting support to manage depressive symptoms\u002Fother stressors. The team's primary knowledge user (D. McNeil, Scientific Director, Maternal Newborn Child and Youth Strategic Clinical Network, Alberta Health Services) advocated for online delivery of the ATTACH™ parent training program. In response, an interdisciplinary team from nursing and software engineering rapidly pivoted to an online delivery format. Critical barriers to using existing commercial technologies emerged, making it essential to develop and implement tailored, user-informed virtual care delivery platforms and tools safe, secure, user-friendly for families already stressed. Innovative user interface design and integrated knowledge transfer approaches will be used to: (a) adapt ATTACH™ for virtual delivery; (b) develop virtual platforms (web-based applications) and tools (mobile apps) for flexible delivery of mental health supports for parents and training for professional facilitators; (c) integrate virtual mental health services into the primary care system promoting program uptake; and (d) design\u002Ftest streamlined and intuitive virtual systems for nimble spread\u002Fscaleup. The project catalyzes and enriches the PIs' research program by crossing disciplines (nursing \\& engineering) in cutting edge research that is responsive to trends in both mental health intervention and web-interface design. The aim is to adapt, develop, design and pilot test virtual (web-based) intervention program to improve children's mental, emotional and behavioral (MEB) health and development. This will be done by building on successful CIHR funded in-person (home or clinic) programs and pivoting to user-engaged program development, adaptation and pilot testing for virtual delivery in the face of COVID19.",[197,198,29,199],"Depression","Addiction","Poverty","2024-05-08",{"date":202,"type":36},"2024-05-10",{"date":204,"type":36},"2021-03-15",{"date":206,"type":19},"2027-12-31",{"name":208,"class":43},"University of Calgary"]