[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"youth\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:youth":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,52,84,116,141,164],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100625180","supporting-social--economic-equity-disrupting-cycles-of-homelessness-and-nurturing-growth--empowerment-100625180",false,"NCT07419282","Supporting Social & Economic Equity, Disrupting Cycles of Homelessness, And Nurturing Growth & Empowerment","Supporting Social & Economic Equity, Disrupting Cycles of Homelessness, And Nurturing Growth & Empowerment (SEED CHANGE): A Mixed Methods Quasi-experimental Trial of Economic, Social, and Identity Capital Supports for Youth Transitioning Out of Homelessness in Ontario, Canada","SEED CHANGE","Inclusion Criteria:\n\n* Aged 18 - 24 years\n* Experienced homelessness (defined as unstable\u002Ftime-limited housing arrangements like shelter stays, foster care, or couch surfing) for at least seven consecutive days in the past year\n* Living in market rent housing (defined as non-subsidized housing, inclusive of both formal and informal rental agreements) in the Greater Toronto Area or Niagara Region for at least one month preceding study start\n* Willing to actively participate in all components of the intervention\n* Able to legally work in Canada (includes having a valid Social Insurance Number)\n* Able to provide free and informed consent\n* Able to understand English well enough to give consent and participate in the intervention and data collection\n\nExclusion Criteria:\n\n* In imminent danger of losing their housing (e.g., facing eviction)\n* Planning to move out of the Greater Toronto Area or Niagara Region in the next 18 months\n* Employed full-time or enrolled in an education or training program that requires a long-term (\\>4 weeks) full-time work placement (coinciding with the duration of the study intervention)\n* Receiving rent subsidies (does not include shelter allowance through social welfare programs such as Ontario Works or the Ontario Disability Support Program)\n* Enrolled in a program or study with features similar to the SEED CHANGE intervention (e.g., 1:1 coaching, supported employment, group program targeting identity\u002Fsocial capital)","ALL","18 Years","24 Years",{"count":21,"type":22},42,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of the SEED CHANGE pilot study is to co-design and test a wraparound intervention for young people transitioning away from homelessness. This study will provide information about the types of supports these young people need to live meaningful and thriving lives, and the best ways to deliver these supports. The main questions it aims to answer are:\n\n* Is the wraparound intervention feasible? (i.e., Will young people engage in the study and supports?)\n* Is the wraparound intervention acceptable? (i.e., Do young people find the supports satisfactory and\u002For beneficial?)\n\nParticipants will engage in an 18-month wraparound intervention including the following supports:\n\n* Job Placement\n* Housing Stabilization Funds\n* Grocery Supplements\n* Community Connections Worker\n* Coaching\n* Tools for Intentional Living Program",[28,29],"Homelessness","Youth",[31,32,33,34,35,36,37,38],"youth","coach","employment","homelessness","transition","socioeconomic inclusion","identity capital","social capital","RECRUITING","2026-06-11",{"date":42,"type":43},"2026-06-15","ACTUAL",{"date":45,"type":43},"2026-02-25",{"date":47,"type":22},"2029-08",{"name":49,"class":50},"Unity Health Toronto","OTHER",1,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":60,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":23,"phases":66,"briefSummary":67,"conditions":68,"keywords":70,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":83},"100620539","the-effects-of-corrective-exercise-and-kt-applications-in-young-basketball-players-100620539","NCT07358936","THE EFFECTS OF CORRECTIVE EXERCISE AND KT APPLICATIONS IN YOUNG BASKETBALL PLAYERS","THE EFFECTS OF CORRECTIVE EXERCISE AND KİNESİOTAPE APPLICATIONS ON PERFORMANCE AND FUNCTIONAL MOBILITY IN YOUNG BASKETBALL PLAYERS","KT:KINESIOTAPE","Inclusion Criteria:\n\n* The male athlete's sport must be basketball.\n* The male athlete must be between 9 and 16 years old.\n\nExclusion Criteria:\n\n* Having undergone any surgical operation within the last 6 months.\n* Having suffered a lower\u002Fupper extremity injury within the last 3 months.\n* The volunteer does not wish to continue the study.\n* Athletes for whom the necessary assessments or procedures could not be performed were excluded.",true,"MALE","9 Years","16 Years",{"count":65,"type":22},45,[25],"The main objective of this research is to comparatively examine the effects of corrective exercise programs and kinesio taping (KT) applications on performance parameters and functional mobility in adolescent male basketball players. Kinesio taping is used with the aims of regulating muscle tone, increasing proprioception, improving circulation, and supporting pain management. In this context, corrective exercises are applied to correct movement disorders, eliminate musculoskeletal imbalances, and improve the functional movement quality in athletes. Although the effects of both methods on the performance parameters and functional mobility of athletes have been examined separately in the literature, a direct comparative study in adolescent basketball players is noticeable.",[29,69],"Sport Performance",[71,72,73,69],"YOUNG BASKETBALL PLAYERS","Corrective Exercise","Kinesiotape","2026-03-11",{"date":76,"type":43},"2026-03-13",{"date":78,"type":43},"2026-02-15",{"date":80,"type":22},"2026-07-16",{"name":82,"class":50},"Vedat Göken",2,{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":88,"acronym":4,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":17,"minAge":90,"maxAge":91,"enrollmentInfo":92,"targetDuration":4,"studyType":23,"phases":94,"briefSummary":95,"conditions":96,"keywords":99,"overallStatus":106,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":4},"100623871","piloting-a-brief-online-intervention-for-suicidality-in-sexual-and-gender-minority-youth-100623871","NCT07402265","Piloting a Brief, Online Intervention for Suicidality in Sexual and Gender Minority Youth","Inclusion Criteria:\n\n* Resident of Canada\n* Fluent in English\n* Youth (i.e., 13-25 years)\n* Identifies as a sexual and\u002For gender minority (i.e., any sexual identity excluding heterosexual and\u002For any gender identity excluding cisgender)\n* Endorses experiencing any suicidal ideation within the past 6 months\n* Access to a computer and able to participate virtually\n\nExclusion Criteria:\n\n* Does not meet the inclusion criteria","13 Years","25 Years",{"count":93,"type":22},250,[25],"Sexual and gender minority youth (i.e., LGBTQ+ individuals) are at elevated risk for suicidal thoughts compared to cisgender\u002Fheterosexual youth and there is increased demand for programs and treatments tailored to this population. The current study seeks to pilot a brief, online, self-guided intervention for suicidal thoughts designed for sexual and gender minority youth to test if this intervention is acceptable to this population and if completing this intervention significantly decreases suicidal thoughts.",[97,98,29],"Suicidal Thoughts","Sexual and Gender Minorities",[100,98,29,101,102,103,104,105],"Suicidal thoughts","Brief","Online","Self-Guided","Self-Compassion","Self-Neutrality","NOT_YET_RECRUITING","2026-02-06",{"date":109,"type":43},"2026-02-11",{"date":111,"type":22},"2026-02-01",{"date":113,"type":22},"2026-09-30",{"name":115,"class":50},"Western University",{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":4,"eligibilityCriteria":122,"healthyVolunteers":11,"sex":17,"minAge":123,"maxAge":19,"enrollmentInfo":124,"targetDuration":4,"studyType":23,"phases":126,"briefSummary":127,"conditions":128,"keywords":131,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":133,"startDateStruct":135,"completionDateStruct":137,"leadSponsor":139,"locationsCount":51},"100528095","cbt-i-versus-cbt-iact-for-youths-with-insomnia-and-anxiety-100528095","NCT06156306","CBT-I Versus CBT-I+ACT for Youths With Insomnia and Anxiety","Effectiveness of CBT-I and CBT-I Combined ACT for Insomnia and Anxiety Symptoms in Youth: A Randomised Control Trial","Inclusion Criteria:\n\nYouth who meet the following criteria would be eligible for taking part in this trial:\n\ni. Chinese youth aged 15-24 years old, ii. Presence of insomnia problems as defined by insomnia severity index (ISI) using cut-off of 9, which has been locally validated cut off for detecting clinical insomnia), iii. Presence of anxiety features as defined by General Anxiety Disorder-7 (GAD-7) using cut-off of 10 for detecting clinical anxiety, iv. Ability to listen, speak, and read Chinese and Cantonese, and v. Written informed consent of participation into the study is given by youth and his\u002Fher parent's if under 18 years old; In addition, individual assent will also be obtained for subjects under age 18 years old vi. Possession of smartphone\n\nExclusion Criteria:\n\nA youth would be excluded from the study if meeting one or more of the following criteria:\n\ni. A clinical diagnosis of psychosis, schizophrenia, bipolar disorders, or intellectual disability ii. Having a diagnosed sleep disorder (e.g. delayed sleep phase and narcolepsy) that may potentially contribute to the disruption of sleep quantity and quality as determined by validated Diagnostic Interview for Sleep Patterns and Disorders (DISP) iii. Having a clinically significant suicidality (presence of suicidal ideation with a plan or an attempt) as assessed by The Structured Clinical Interview (SCID) iv. Currently receiving psychological treatment and\u002For pharmacological treatment for insomnia or anxiety disorder.","15 Years",{"count":125,"type":22},50,[25],"Insomnia in adolescents and youth is a long-standing public health concern due to its high prevalence and association with various physical and mental health problems. Insomnia and psychiatric disorders are highly comorbid and intercorrelated in adolescents. Among all mental disorders, anxiety has been shown to be have high comorbidity with insomnia, affecting approximately 30% of individuals. CBT for insomnia (CBT-I) has been shown to be effective in improving sleep complaints and short-term improvement in mood while previous systematic reviews of interventional studies have demonstrated the effectiveness of acceptance and commitment therapy (ACT) interventions in treating insomnia, both as a primary condition and with other physical and\u002For mental health comorbidities. This study aims to compare the effect of CBT-I and CBT-I combined ACT in improving anxiety symptoms in youth.",[129,130,29],"Insomnia","Anxiety",[129,130,29],"2025-07-08",{"date":134,"type":43},"2025-07-10",{"date":136,"type":43},"2023-12-15",{"date":138,"type":22},"2025-12-31",{"name":140,"class":50},"Chinese University of Hong Kong",{"id":142,"slug":143,"hasResults":11,"nctId":144,"briefTitle":145,"officialTitle":146,"acronym":147,"eligibilityCriteria":148,"healthyVolunteers":11,"sex":17,"minAge":123,"maxAge":19,"enrollmentInfo":149,"targetDuration":4,"studyType":23,"phases":151,"briefSummary":152,"conditions":153,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":51},"100430809","pilot-rct-of-self-stigma-treatment-for-first-episode-psychosis-100430809","NCT04889911","Pilot RCT of Self-stigma Treatment for First Episode Psychosis","Development of a Stage-specific Adaptation of a Self-stigma Intervention for People Recovering from a First Episode of Psychosis","NECT-YA","Inclusion Criteria:\n\n1. Meets criteria for FEP youth based on the following definition: age 15-24, onset of psychotic symptoms within the last 5 years, and an absence of a primary substance use or mood disorder that could be causing the psychotic symptoms (confirmed by program eligibility);\n2. Meets criteria for moderate (defined as a mean score of 1-1.5 on the 0-3 scale of the Internalized Stigma of Mental lllness Scale \\[ISMI\\]) or elevated (defined as a mean score of 1.5-3 on the 0-3 scale of the ISMI) self-stigma;\n3. Speaks English well enough to complete assessments and participate in groups;\n4. Is able to provide informed consent to participate.\n\nExclusion Criteria:\n\nDoes not meet any of the above inclusion criteria.",{"count":150,"type":22},40,[25],"The overall purpose of the proposed exploratory intervention development application, is to conduct research that will inform the adaptation and preliminary testing of NECT modified for youth (aged 15-24) with first episode psychosis (FEP), targeting self-concept and illness conceptions to increase treatment engagement. The specific aims of the project are to: 1) adapt NECT to be responsive to the needs and preferences of youth with FEP, and 2) Assess the feasibility, acceptability and preliminary effectiveness of the modified intervention (NECT-YA) combined with coordinated specialty care (CSC) services, compared to CSC services alone, in a small (n = 40) RCT.",[154,29],"First Episode Psychosis","2025-03-19",{"date":157,"type":43},"2025-03-24",{"date":159,"type":43},"2023-08-01",{"date":161,"type":22},"2025-08",{"name":163,"class":50},"John Jay College of Criminal Justice, City University of New York",{"id":165,"slug":166,"hasResults":11,"nctId":167,"briefTitle":168,"officialTitle":169,"acronym":170,"eligibilityCriteria":171,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":172,"targetDuration":4,"studyType":23,"phases":174,"briefSummary":175,"conditions":176,"keywords":180,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":184,"lastUpdatePostDateStruct":185,"startDateStruct":187,"completionDateStruct":189,"leadSponsor":191,"locationsCount":51},"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":173,"type":22},200,[25],"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.",[177,178,29,179],"Primary Health Care","Interpersonal Violence","Pregnancy",[29,179,181,182,183],"Primary care","Virtual patient","Interpersonal violence","2024-04-26",{"date":186,"type":43},"2024-04-29",{"date":188,"type":43},"2024-04-01",{"date":190,"type":22},"2028-06-30",{"name":192,"class":193},"Region Stockholm","OTHER_GOV"]