[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"interpersonal-violence\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:interpersonal-violence":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,45,76],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100650345","program-for-alleviating-relationship-trauma-and-stress-for-intimate-partner-violence---randomized-control-trial-100650345",false,"NCT07747766","Program for Alleviating Relationship Trauma and Stress for Intimate Partner Violence - Randomized Control Trial","PARTS-IPV RCT","Inclusion Criteria:\n\n* Must be male-identifying or prefer to be in a male-identifying group;\n* Must be a resident of Washington state;\n* Must be court-referred to a treatment program for using violence with an intimate partner;\n* Have sufficient English fluency and literacy skills to understand the consent process, procedures and questionnaires and have the ability to provide written informed consent;\n* Have access to the internet and an electronic device with adequate data capacity; to complete questionnaires online and attend online video conference groups;\n* Must be available and willing to attend at least 17 out of 20 scheduled online group sessions; and\n* Must be available and willing to complete the online computerized assessments, and phone interviews.\n\nExclusion Criteria:\n\n* Insufficiently stable housing or internet connection to be able to join at least 17 group sessions;\n* Current participation in another experimental research study;\n* Expected medical hospitalization in the next six months from study enrollment period;\n* Current or expected physical incarceration (excluding house arrest or other forms of electronic monitoring) in the next six months from study enrollment period;\n* Inpatient hospitalization for mental health, substance use, suicide attempt or self-harm within past three months;\n* Inability to participate safely in the study intervention and without disrupting the group (in the opinion of principal investigator OR meeting any of the following criteria)\n* Past year history of a psychotic disorder or clinician confirmed active psychosis assessed by the Structured Clinical Interview for DSM-5 (SCID-5);\n* Bipolar I disorder history or current severe level of mania assessed by the Structured Clinical Interview for DSM-5 (SCID-5);\n* Acute suicidality with intent will be excluded from the study (Structured Clinical Interview for DSM-5 \\[SCID-5\\]);\n* High levels of Psychopathy as defined by self-report psychopathy checklist (SRP-4);\n* Self-injurious behavior in past three months will require clinical assessment prior to participation in the program;\n* Acute homicidality with plan and\u002For intent;\n* Inability to join a group without intoxication.\n* Prior experience or exposure with Internal Family Systems (e.g. IFS therapy, IFS groups or retreats, current IFS practice, etc.)","MALE","18 Years",{"count":19,"type":20},48,"ESTIMATED","INTERVENTIONAL",[23],"NA","This research study investigates the feasibility of a randomized control trial of a group-based treatment program for reducing stress, trauma, substance use, and use of violence among individuals who were court-mandated to attend a program after committing an act(s) of domestic violence. The study is in a 2-arm design with an intervention group and a control group.",[26,27],"Individuals Who Use Violence","Interpersonal Violence",[27,29,30,31],"Domestic Violence","Internal Family Systems (IFS)","Program For Alleviating Relationship Trauma and Stress (PARTS)","NOT_YET_RECRUITING","2026-07-31",{"date":35,"type":36},"2026-08-05","ACTUAL",{"date":38,"type":20},"2026-08-01",{"date":40,"type":20},"2027-07-31",{"name":42,"class":43},"Cambridge Health Alliance","OTHER",2,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":54,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":21,"phases":59,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100550052","strengthening-the-connections-to-opportunities-for-prevention-engagement-100550052","NCT06442046","Strengthening the Connections to Opportunities for Prevention Engagement","Strengthening the Connections to Opportunities for Prevention Engagement (SCOPE)","SCOPE","Inclusion Criteria:\n\n* At least 8 years of age and not older than 17 years of age (until 18th birthday)\n* Hartford resident based on zip code of primary residence or parent report?\n* Accompanied by a parent or guardian who can provide consent\n* Capable of providing assent\u002Fconsent\n* Able to provide consent in English or Spanish\n* Presenting at CT Children's during recruitment hours\n\nExclusion Criteria:\n\n* Patients whose primary complaint is for behavioral health\n* Patients in Connecticut Department of Children and Families (DCF) or police custody",true,"ALL","8 Years","17 Years",{"count":58,"type":20},225,[23],"The Strengthening the Connections to Opportunities for Prevention Engagement (SCOPE) project will create a pathway for children and families from the City of Hartford to connect with a Connecticut Children's Care Coordinator (CC) in an effort to reduce levels of violence exposure.",[27,62],"Structural Violence",[64],"youth violence prevention","RECRUITING","2025-09-24",{"date":68,"type":36},"2025-09-25",{"date":70,"type":36},"2024-08-19",{"date":72,"type":20},"2026-06-30",{"name":74,"class":43},"Kevin Borrup",1,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":54,"minAge":17,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":21,"phases":86,"briefSummary":87,"conditions":88,"keywords":92,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":75},"100540854","identification-of-interpesonal-violence-100540854","NCT06322251","Identification of Interpesonal Violence","Identifying Intimate Partner Violence: an Intervention Study in Health Care Using a Standardised Questionnaire and Virtual Patients","ViP","Inclusion criteria:\n\n* All health care staff who meet patients at the included study sites are elegible for the study\n* Midwives, MDs, psychologists, social workers, nurses etc.\n\nExclusion criteria:\n\n\\- Health care staff who does not want to participate",{"count":85,"type":20},200,[23],"The goal of this study is to increase primary care professional's ability to identify individuals exposed to intimate partner violence (IPV) in primary health care settings.\n\nThe main questions it aims to answer are\n\n1. To what extent do the following three interventions contribute to identify potential victims of IPV: (1) the use of a standardized questionnaire that screens exposure to IPV, (2) staff using tailored virtual patients for clinical training on IPV and (3) a combination of interventions 1 and 2?\n2. Which intervention do primary care professionals experience as most effective in increasing the ability to identify and respond to victims of IPV?\n\nParticipants will be divided to apply one of the three interventions in their health care setting: 1) a standardized questionnaire to patients, 2) virtual patients tailored to health professionals, and 3) a combination of 1 and 2.\n\nPre-and post-measurement of the health professionals identification of patients exposed to IPV will will be used to explore the effect of the interventions.\n\nFocus group interviews with the participating health professionals will be a qualitative complement. The participants will be asked about what intervention they experience as the most effective in increasing the ability to identify victims of IPV.",[89,27,90,91],"Primary Health Care","Youth","Pregnancy",[90,91,93,94,95],"Primary care","Virtual patient","Interpersonal violence","2024-04-26",{"date":98,"type":36},"2024-04-29",{"date":100,"type":36},"2024-04-01",{"date":102,"type":20},"2028-06-30",{"name":104,"class":105},"Region Stockholm","OTHER_GOV"]