[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"psychiatry\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:psychiatry":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,44,75],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":4},"100644554","effects-of-a-qi-gong-program-on-dissociative-symptoms-in-patients-who-have-experienced-childhood-trauma-a-randomized-controlled-trial-qi-t-100644554",false,"NCT07670663","Effects of a Qi Gong Program on Dissociative Symptoms in Patients Who Have Experienced Childhood Trauma: a Randomized Controlled Trial (Qi-T)","Effects of a Qi Gong Program on Dissociative Symptoms in Patients Who Have Experienced Childhood Trauma: a Randomized Controlled Trial","Qi-T","Inclusion Criteria:\n\n* 18 years of age or older\n* A score above the 10th percentile on the Dissociative Experience Scale-II (DES-II)\n* A score above 2 on the ACE scale (Adverse Childhood Experiences by Felitti et al., 1998)\n* A medical certificate attesting to the participant's fitness to practice Qigong\n* A person enrolled in or receiving benefits from a social security program\n* Free, informed, and written consent signed by the participant and the investigator (no later than the day of enrollment and prior to any examination required by the study).\n\nExclusion Criteria:\n\n* In a suicidal crisis\n* In a hallucinatory crisis\n* Experiencing a major depressive episode\n* Unstabilized\n* Pregnant women\n* Those who do not understand French\n* Under guardianship or conservatorship\n* Under judicial protection","ALL","18 Years",{"count":20,"type":21},90,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to evaluate whether participation in 12 Qi Gong sessions (intervention group), compared with usual care without Qi Gong (control group), reduces dissociative symptoms, as measured by the Dissociative Experience Scale-II (DES-II), between T0 and T1, in outpatients hospitalized for psychiatric disorders related to aversive experiences during childhood.\n\nThe main questions it aims to answer are:\n\n\\- a) To assess whether participation in the Qi Gong program leads to a reduction in symptoms related to complex trauma, b) To assess whether participation in the Qi Gong program leads to an increase in the level of mindfulness c) To explore whether the effect of the Qi Gong program on reducing dissociative symptoms varies according to participants' baseline level of dissociation (Dissociative Experiences Scale-II ) d) To explore whether the effect of the Qi Gong program on reducing dissociative symptoms is sustained over time e) To explore the experiences of patients who participated in the Qi Gong sessions following the intervention.\n\nThis is a randomized controlled trial with parallel groups:\n\n* Intervention group: participation in 12 Qi Gong sessions led by a trained professional, in addition to standard care\n* Control group: standard care, without access to Qi Gong sessions during the study period.\n\nParticipants will be required to:\n\n* complete 3 questionnaires (DES-II, ITQ, MAAS)\n* attend one Qi Gong session per week for 12 weeks (including a group debriefing) or receive standard care at a medical-psychological center (without Qi Gong)\n* complete the same questionnaires (DES-II, ITQ, MAAS) after the 12 weeks\n* complete the DES-II questionnaire 2 months later",[27],"Psychiatry",[29,30,31],"dissociative symptoms","childhood trauma","Qi- Qong","NOT_YET_RECRUITING","2026-06-22",{"date":35,"type":36},"2026-06-26","ACTUAL",{"date":38,"type":21},"2026-09",{"date":40,"type":21},"2029-03",{"name":42,"class":43},"Centre Hospitalier Universitaire de la Réunion","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":17,"minAge":18,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":54,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":74},"100641401","use-of-football-in-programs-to-reduce-stigma-toward-mental-illness-a-comparison-of-the-effectiveness-of-contact-interaction-and-video-based-approaches-100641401","NCT07658066","Use of Football in Programs to Reduce Stigma Toward Mental Illness: A Comparison of the Effectiveness of Contact Interaction and Video-Based Approaches","Inclusion Criteria:\n\n* University students currently enrolled, aged between 18 and 30 years.\n* In good physical condition with no contraindications to exercise (i.e., not diagnosed by a physician or advised to avoid physical activity, and with no items selected on the PAR-Q+ \\[Physical Activity Readiness Questionnaire for Everyone\\]).\n* Able to follow the study procedures and provide signed informed consent.\n\nExclusion Criteria:\n\n* Individuals who are unable to safely participate in football activities due to intellectual disability, pregnancy, head injury, cardiovascular disease, or other neuromuscular or musculoskeletal disorders.\n* Individuals who are unable to effectively participate in the intervention program or complete assessments due to significant emotional disturbances, personality disorders, substance (alcohol) abuse, or severe mental illness.",true,"30 Years",{"count":53,"type":21},210,[24],"The goal of this clinical trial is to evaluate the effectiveness of football-based interventions in reducing stigma toward mental illness among university students. The main questions it aims to answer are:\n\n* Does participating in a contact-based education program involving football help reduce stigma toward mental illness among university students?\n* What are the effects of three different intervention methods on reducing stigma toward mental illness?\n\nResearchers will compare the traditional contact-based education program with the other two interventions to evaluate their differences in effectiveness.\n\nParticipants will:\n\n* Be randomly assigned to one of the three intervention groups.\n* Complete online assessments to measure attitudes toward mental illness before and after the intervention.\n* Participate in qualitative interviews to provide in-depth feedback on their experiences and perceptions.",[27,57],"Rehabilitation",[59,60,61,62,63],"mental illness","Psychiatric disorders","physical activity","stigma","exercise","RECRUITING","2026-06-16",{"date":67,"type":36},"2026-06-18",{"date":69,"type":36},"2026-03-02",{"date":71,"type":21},"2027-10-31",{"name":73,"class":43},"Kaohsiung Medical University Chung-Ho Memorial Hospital",1,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":86,"conditions":87,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":74},"100505006","nationwide-uniform-scientific-evaluation-of-flexible-and-integrated-treatment-projects-from-2022-onwards-100505006","NCT05855720","Nationwide Uniform Scientific Evaluation of Flexible and Integrated Treatment Projects From 2022 Onwards","Bundesweit Einheitliche Wissenschaftliche Evaluation Von Modellvorhaben Nach § 64b SGB V ab 2022","EVA64_2","Inclusion Criteria:\n\n* treatment in any of the participating hospitals or control hospitals within recruitment phase (number of hospitals will be fix until June 2026)\n* being insured with any of the participating SHI funds\n\nExclusion Criteria:\n\n* less than one year follow-up data available",{"count":84,"type":21},30000,"OBSERVATIONAL","This study is an evaluation of flexible and integrated psychiatric care models (according to § 64b of the German Social Code Book V (SGB V)) (FIT) including new FIT projects starting after 2022 and the prolongation of any of 19 already established FIT projects (mainly at German psychiatric hospitals). The central concern of this evaluation is to answer the question whether FIT care offers advantages over standard care. The orientation of model care is a more cross-sectoral provision of services through more flexible psychiatric treatment intensities. However, FIT program structures depend on the individual situation and organization of the FIT hospital together with the participating statutory health insurance (SHI) funds.",[88,89,90,91,27,92,93],"Mental Health","Cross-sectoral Treatment","Flexible and Integrated Treatment","FIT","Evaluation Study","Cohort Studies","2024-08-06",{"date":96,"type":36},"2024-08-07",{"date":98,"type":36},"2019-01-01",{"date":100,"type":21},"2041-07",{"name":102,"class":43},"Technische Universität Dresden"]