[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sexual-trauma\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sexual-trauma":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,71,110],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100573048","recovery-oriented-group-therapy-for-veteran-men-with-military-sexual-trauma-100573048",false,"NCT06741202","Recovery-oriented Group Therapy for Veteran Men With Military Sexual Trauma","Recovery-oriented Group Therapy for Veteran Men With Military Sexual Trauma (CDA 23-054)","Inclusion Criteria:\n\n* Eligible participants include any individual who identifies as a Veteran cisgender man with a history of MST, English-speaking, 18 years of age or older, and enrolled in the VAGLA. Participants must:\n\n  * comprehend and sign the informed consent form\n  * report a history of MST\n  * agree to complete research instruments\n* Because we are looking for a range of impact among men MST survivors, participants will not be excluded based on psychiatric diagnosis\n\nExclusion Criteria:\n\n* Per chart review conducted by the PI prior to screening and patient contact, Veterans will be excluded if they demonstrate:\n\n  * severe suicidal or homicidal ideation, defined using the Columbia Suicide Severity Rating Scale (C-SSRS) and behavioral flags per chart review\n  * severe and uncontrolled substance abuse (identified through current treatment of a substance use disorder in chart)\n  * illness that inhibits engagement in study procedures (e.g., inability to attend in-person visits)\n  * inability to self-consent to participate\n  * completion of CPT, PE, or the MMG 5 or fewer years ago\n  * concurrent enrollment in a trauma-focused intervention\n* Through chart review, Veterans who dropped out of these treatments after 3 sessions will still be eligible as this is considered \"early dropout.\"\n* If immediate clinical attention is warranted, Veterans will receive immediate care via procedures outlined in the human subjects protection plan","MALE",{"count":18,"type":19},32,"ESTIMATED","INTERVENTIONAL",[22],"NA","VA has identified military sexual trauma (MST) as one of its highest priorities. MST is associated with increased prevalence of PTSD and depression, substance use disorders, suicide, difficulties maintaining relationships and employment, and homelessness. Yet important gender differences have been identified among MST survivors and many man may experience stigma and shame related to masculinity and sexuality. While gender-based shame appears central to MST-related distress and treatment underutilization, gender has often been overlooked in establishing evidence-based approaches, and no VA MST-related treatment has been developed specifically for men. To address this critical service gap, this study will collect data on improving treatment strategies and patient engagement for men with histories of MST. It will seek to develop strategies for enhancing a 12-session, gender-tailored group therapy for men MST survivors previously developed and implemented by the principal investigator. It will interview Veteran participants and mental health clinicians, conduct a pilot randomized trial, and evaluate feasibility within the VA, with the long-term goal of national implementation",[25],"Sexual Trauma",[27,28,29],"military sexual trauma","veteran men","group therapy","NOT_YET_RECRUITING","2026-05-05",{"date":33,"type":34},"2026-05-06","ACTUAL",{"date":36,"type":19},"2026-10-05",{"date":38,"type":19},"2029-12-31",{"name":40,"class":41},"VA Office of Research and Development","FED",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":50,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":20,"phases":55,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":42},"100605693","voices-of-transformation-a-deep-dive-into-the-struggles-and-successes-of-reclaiming-sexuality-after-sexual-trauma-100605693","NCT07165834","Voices of Transformation: A Deep Dive Into the Struggles and Successes of Reclaiming Sexuality After Sexual Trauma","Take Your Sexuality Back - a Feasibility Study of a New Intervention for Sexually Traumatized Women","Inclusion Criteria:\n\n1. A history of sexual trauma\n2. Experience trauma-related sexual problems\n3. Age between 18 and 65 years\n4. Enough competence in Norwegian to participate in a psychoeducational group.\n\nExclusion Criteria:\n\n1. Acute suicidality\n2. Serious substance abuse interfering with treatment\n3. Severe dissociative or psychotic disorders\n4. Current life crisis interfering with treatment\n5. Living in an abusive relationship. -","FEMALE","18 Years","65 Years",{"count":54,"type":19},20,[22],"This study aims to gain insight into the experiences of participants in the \"Take Your Sexuality Back\" intervention groups, evaluate the intervention's acceptability, and identify necessary modifications. This study is part of a larger project that seeks to establish a scientific basis for this innovative, group-based treatment to help women who have experienced sexual trauma heal their sexuality. Before implementing the intervention in the healthcare system and initiating a larger randomized controlled trial, the investigators will evaluate the intervention's feasibility and potential efficacy, as well as gain a more comprehensive understanding of treatment outcomes. In addition to collecting quantitative data, it is crucial to gather qualitative data on participants' experiences. In this study, data will be obtained through in-depth interviews with group participants after they complete the intervention.",[58,59,25],"Sexual Abuse","Posttraumatic Stress Symptom","RECRUITING","2026-04-28",{"date":63,"type":34},"2026-05-04",{"date":65,"type":34},"2025-09-15",{"date":67,"type":19},"2028-12",{"name":69,"class":70},"Sykehuset Telemark","OTHER_GOV",{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":77,"eligibilityCriteria":78,"healthyVolunteers":11,"sex":79,"minAge":80,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":20,"phases":84,"briefSummary":85,"conditions":86,"keywords":90,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":5},"100608373","effect-study-of-smart-treatment-for-youth-100608373","NCT07200713","Effect Study of SMART Treatment for Youth","A Randomized Controlled Evaluation of Sensory Motor Arousal Regulation Treatment (SMART) for Youth With Developmental Trauma and Self-regulation Difficulties","UTVID","Inclusion criteria:\n\nThese are based on the Developmental Trauma Disorder Semistructured Interview (DTD-SI), which has four domains (A-D). Based on the DTD-SI, which is detailed below, inclusion requires:\n\n* The presence of developmental trauma history (domain A)\n* One symptom in each of the domains B-D\n* At least four symptoms (of a maximum 15) in domains B-D considered together\n\nDomains A to D above refers to the following:\n\n* Domain A. Lifetime contemporaneous exposure to developmental trauma, defined as either (i) Interpersonal victimization: physical or sexual abuse or assault, domestic\u002Fintimate partner violence, bullying, harassment, exploitation, trafficking, hate crimes, or racial\u002Fethnic\u002Fidentity trauma, or (ii) Primary caregiving system attachment disruption: caregiver change or prolonged separation, gross neglect (physical, medical, emotional), psychological maltreatment (emotional abuse, emotional neglect, parental hostility or over-controlling), caregiver impairment due to mental illness or substance abuse, or chronic medical condition (by child or caregiver)\n* Domain B. Affective and somatic dysregulation: (i) Emotion dysregulation, (ii) Somatic dysregulation, (iii) Impaired awareness or dissociation of emotions and body, (iv) Impaired capacity to describe emotions or bodily states\n* Domain C. Attentional and behavioral dysregulation: (i) Threat-related rumination, (ii) Impaired capacity for self protection, (iii) Maladaptive self-soothing, (iv) Habitual or reactive self-harm, (v) Inability to initiate or sustain goal-directed behavior\n* Domain D. Self and relational dysregulation: (i) Persistent extreme negative self-perception, (ii) attachment insecurity and disorganization, (iii) Extreme persistent distrust, defiance or lack of reciprocity in close relationships, (iv) Reactive physical or verbal aggression, (v) Psychological boundary deficits, (vi) Impaired capacity to regulate empathic arousal\n\nExclusion Criteria:\n\n* Active psychosis\n* Not fluent in Norwegian language\n* Developmental challenges - IQ \\\u003C 70\n* Has previously used SMART room","ALL","7 Years","17 Years",{"count":83,"type":19},120,[22],"The goal of this clinical trial is to learn if Sensory motor arousal regulation treatment (SMART) works better than treatment as usual (TAU) to treat youth 7-17 years with complex trauma histories and self-regulation difficulties. The study also will investigate which patients will benefit more from SMART (treatment effect heterogeneity) and whether therapeutic alliance mediates effect. The main hypotheses the trial aims to answer are:\n\n1. Main effects: The SMART model approach will be more effective than ordinary treatment (control condition), in terms of improvement from therapy starts to 6 and 12 months follow up, for:\n\n   1. Regulatory capacities of emotions and bodily states, attention and behavior, and self and social relations\n   2. Trauma symptoms of re-experiencing, avoidance\u002F numbness and hyperarousal and sense of threat (core PTSD symptoms) and disturbances in self-organization (affect, self-concept; relations - core complex PTSD symptoms)\n   3. Internalizing symptoms (somatic complaints, anxiety symptoms and depression symptom severity) and Externalizing symptoms (conduct problems, aggression, inattention, and social problem severity)\n   4. Psychosocial strengths - prosocial behavior, subjective well-being and impairment in peer relationships, family relationships, and academic\u002Fschool functioning\n2. Exploration of mediation: When comparing SMART and ordinary treatment (TAU), (i) therapeutic alliance is higher in SMART, and (ii) a better treatment effect in SMART is partially mediated by therapeutic alliance\n\n3\\. Exploration of treatment effect heterogeneity (moderators): Effects of SMART treatment compared to TAU vary between: patients with low versus high level of self-regulation difficulties (full vs partial Developmental trauma disorder), patients with extensive vs less extensive developmental trauma exposure, adolescents (13-17 years) vs younger children (7-12 years), and patients exposed to trauma early in life vs in their teens\n\nAt each site, eligible participants are randomized to SMART or ordinary treatment\u002F TAU. Investigators acquire study data at baseline and outcome data at follow up after 6 and 12 months, and measure therapeutic alliance twice during the treatment process.",[87,88,25,89],"Stress Disorders, Traumatic","Psychological Trauma","Stress Disorders, Post-Traumatic; Mental Disorders",[91,92,93,94,95,96,97,98,99],"Randomized controlled trial","Developmental trauma disorder","self-regulation difficulties","trauma treatment","Sensory motor arousal regulation treatment (SMART)","Children","Youth","Outpatient treatment","Treatment as usual","2025-09-22",{"date":102,"type":34},"2025-10-01",{"date":104,"type":19},"2025-09-25",{"date":106,"type":19},"2027-12-31",{"name":108,"class":109},"Vestre Viken Hospital Trust","OTHER",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":50,"minAge":51,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":20,"phases":118,"briefSummary":119,"conditions":120,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":42},"100604310","a-feasibility-mixed-methods-study-of-the-intervention-take-your-sexuality-back-for-sexually-traumatized-women-100604310","NCT07147855","A Feasibility Mixed Methods Study of the Intervention Take Your Sexuality Back for Sexually Traumatized Women.","Take Your Sexuality Back - a Feasibility Study of a New Intervention for Sexually Traumatized Women: Preliminary Evaluations of Efficacy and Outcome Measurements","Inclusion Criteria:\n\n1. A history of sexual trauma.\n2. Experience trauma-related sexual problems.\n3. Age between 18 and 65 years.\n4. Enough competence in Norwegian to participate in a psychoeducational group.\n\nExclusion Criteria:\n\n1. Acute suicidality.\n2. Serious substance abuse interfering with treatment\n3. Severe dissociative or psychotic disorders.\n4. Current life crisis interfering with treatment.\n5. Living in an abusive relationship. -",{"count":54,"type":19},[22],"This study looks at the potential effects of a new group treatment called \"Take Your Sexuality Back\", designed for women who have experienced sexual trauma. Investigators will collect information in two ways-through forms that participants fill out themselves and through ECG measurements during a stress tests. Data will be collected before the treatment, right after it, and again three months later. When all data are collected and analyzed investigators will carry out in-depth interviews with participants and explore how they felt about being tested and how they understand the results -especially if some numbers look unusual or surprising. The goal with this study is to create a strong foundation for a future larger-scale study of the treatment by testing the methods, estimating the size of possible effects and identify outcome measurements that are experienced as meaningful to the participants.",[121,58,25],"Posttraumatic Stress Symptoms","2025-09-01",{"date":124,"type":34},"2025-09-08",{"date":126,"type":19},"2025-09",{"date":128,"type":19},"2027-09",{"name":69,"class":70}]