[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"well-being-psychological-flourishing\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:well-being-psychological-flourishing":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,49,74,102],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100636483","early-phase-1-micropractices-for-unhoused-lgbtq-youth-100636483",false,"NCT07566273","Micropractices for Unhoused LGBTQ Youth","Developing and Evaluating Collaboratively Designed Mindfulness and Identity-Affirming Practices for Unhoused LGBTQ Youth","Inclusion Criteria:\n\n* Aged 16 to 26 years\n* Self-identify as LGBTQ\n* Currently or recently experiencing housing instability (within the past six months)\n* Have access to a mobile device with internet capability to complete study activities\n\nExclusion Criteria:\n\n* Unable to complete study procedures (e.g., lack of device access)",true,"ALL","16 Years","26 Years",{"count":21,"type":22},200,"ESTIMATED","INTERVENTIONAL",[25],"EARLY_PHASE1","In the present study, the investigators will conduct a pilot randomized controlled trial to evaluate the feasibility, acceptability, and preliminary efficacy of brief, co-designed mindfulness and identity-affirming micropractices for LGBTQ youth and young adults experiencing housing instability. Participants (n = 200, accounting for anticipated attrition) will be randomly assigned to one of two conditions: (1) a mindfulness and identity-based micropractice condition or (2) a structurally equivalent neutral control condition. The intervention content will be developed using a participatory co-design process with members of the target population and standardized prior to trial implementation. The mindfulness and identity condition integrates brief practices targeting present-moment awareness and identity affirmation, whereas the control condition accounts for time and attention without including these components. Assessments will be conducted at baseline, post-intervention, and three-month follow-up. Primary outcomes include feasibility and acceptability, assessed using standardized implementation outcome measures and indicators of intervention adherence. Secondary outcomes include changes in mental health symptoms, psychological and emotional well-being, and substance use. The investigators will evaluate whether the mindfulness and identity-based condition demonstrates greater improvements in outcomes compared to the control condition and will estimate effect sizes to inform the design of future fully powered trials. The intervention will be delivered via a mobile-accessible platform.",[28,29,30],"Well-Being (Psychological Flourishing)","Internalizing Mental Health Symptoms","Substance Abuse",[32,33,34,30,35,29],"Micropractice","Unhoused","Well-Being","LGBTQ","NOT_YET_RECRUITING","2026-04-29",{"date":39,"type":40},"2026-05-05","ACTUAL",{"date":42,"type":22},"2026-10",{"date":44,"type":22},"2027-01",{"name":46,"class":47},"Cornell University","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":16,"sex":17,"minAge":56,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":23,"phases":59,"briefSummary":61,"conditions":62,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":48},"100634541","a-mindfulness-based-intervention-for-hotel-staff-100634541","NCT07541027","A Mindfulness-based Intervention for Hotel Staff","Mindfulness Training for Hotel Staff: A Mixed-Methods Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 18 years or above\n* Currently working in a hotel\n* Cantonese speaker\n* Willing to commit time for the 6-week mindfulness course\n\nExclusion Criteria:\n\n* Individuals who had previously joined a related group mindfulness-based intervention, such as mindfulness-based cognitive therapy (MBCT), mindfulness-based stress reduction (MBSR), or Mindfulness - Finding Peace in a Frantic World (FPFW)\n* Staff members who are mentally unstable or having active suicidal risk","18 Years",{"count":58,"type":22},60,[60],"NA","This research aims to investigate the potential impact of a structured mindfulness-based professional development program on hotel employees and to explore why and how these changes occur during and after the mindfulness intervention through a mixed-methods approach. A 6-week mindfulness intervention with 60 hotel staff from a hotel will be implemented in Hong Kong. Both quantitative and qualitative data will be collected to examine changes in job-related outcomes, wellbeing, and state mindfulness and teachers' lived experiences and perspectives associated with this intervention. Data will be analyzed based on convergent parallel mixed-method approach, such as mixed-effects modeling, mediation analysis, and thematic analysis. This study may provide practical implications for developing evidence-based programs to promote wellbeing and service quality among hotel employees.",[28,63,64],"Work Related Stress","Work Performance","2026-04-27",{"date":67,"type":40},"2026-04-30",{"date":69,"type":22},"2026-06-01",{"date":71,"type":22},"2027-05-31",{"name":73,"class":47},"Chinese University of Hong Kong",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":16,"sex":17,"minAge":80,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":23,"phases":83,"briefSummary":84,"conditions":85,"keywords":88,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":48},"100615855","how-can-we-help-wellbeing-interventions-for-choral-music-ensembles-100615855","NCT07298031","How Can We Help? Wellbeing Interventions for Choral Music Ensembles","Inclusion Criteria:\n\n* Enrolled in 6th through 12th grade at selected schools\n* Enrolled in choir at the selected schools\n\nExclusion Criteria:\n\n* None","10 Years","20 Years",{"count":21,"type":22},[60],"The goal of this clinical trial is to learn if psychology and music based interventions can impact anxiety and overall wellbeing in adolescents enrolled in choral music classes. The main questions it aims to answer are:\n\nDo specific psychology and music based breathing interventions impact anxiety and overall wellbeing in adolescents? Do specific psychology and music based performance anxiety reduction interventions impact anxiety and overall wellbeing in adolescents? Do specific psychology and music based emotion regulation interventions impact anxiety and overall wellbeing in adolescents? Researchers will compare results of pre-test data, post-test data, qualitative interviews, and surveys of adult choral directors to see if there is a measurable impact on adolescent anxiety and overall wellbeing.\n\nParticipants will:\n\n* Use box breathing during choral music warm-ups to connect choral breathing to breathing for anxiety reduction\n* Use \"magnify\" technique to compare cognitive distortions regarding an upcoming performance that may cause anxiety to the most likely realistic outcome\n* Use emotion regulation through song lyrics technique to connect lyrics of choral music repertoire to participants experienced emotions",[86,28,87],"Anxiety","Performance Anxiety",[89,90,91,86,92],"Choral music","Wellbeing","Music","Performance anxiety","2025-12-21",{"date":95,"type":40},"2025-12-29",{"date":97,"type":22},"2026-01",{"date":99,"type":22},"2026-04",{"name":101,"class":47},"Jess Walls",{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":108,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":110,"targetDuration":4,"studyType":23,"phases":112,"briefSummary":113,"conditions":114,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":4},"100574145","psychological-counseling-program-for-alzheimers-patients-caregivers-100574145","NCT06755476","Psychological Counseling Program for Alzheimer's Patients' Caregivers","The Effect of Psychological Counseling Program (PsychoCP) for Alzheimer's Patients' Caregivers on Perceived Stress, Psychological Well-Being and Caregiver Burden","PsychoCP","Inclusion Criteria:\n\n* Providing informal care to an individual with mild or moderate Alzheimer's disease\n* Being a primary caregiver\n* Providing care to the patient for at least six months\n* Providing care to the patient for at least six hours per day\n* Being literate\n* Being able to speak and understand Turkish\n* Being 18 years of age or older\n* Being willing and able to participate in the study\n\nExclusion Criteria:\n\n* Not being able to understand questions and express ideas\n* Having a psychiatric disorder\n* Not receiving any therapy services during the study",{"count":111,"type":22},80,[60],"Purpose: To investigate the effects of a psychological counseling program (PsychoCP) applied to caregivers of Alzheimer's patients on perceived stress, psychological well-being and care burden.\n\nDesign: The study will be conducted in a pre-test post-test control group, randomized controlled experimental research design.\n\nMethod: The study is planned to be carried out in Bağcılar Municipality Vefahâne Life Center, Antalya Alzheimer Patients and Patient Relatives Meeting Center and Osmaniye Family and Social Policies Directorate. The sample of the study will consist of 80 caregivers. They will be assigned to intervention (n=40) and control groups (n=40) by randomization.\n\nHypotheses Hypothesis1: The perceived stress level of caregivers who received PsychoDP is lower than those who did not receive PsychoCP.\n\nHypothesis2: The psychological well-being levels of caregivers who received PsychoDP are higher than those who did not receive PsychoCP.\n\nHypothesis3: The care burden of caregivers who received PsychoDP is lower than those who did not receive PsychoCP.",[115,116,117,28,118],"Alzheimer Disease","Caregivers of Alzheimer's Disease or Memory Problem Patients","Perceived Stress","Care Burden","2024-12-24",{"date":121,"type":40},"2025-01-01",{"date":123,"type":22},"2025-02-15",{"date":125,"type":22},"2025-08-15",{"name":127,"class":47},"Aydan Akkurt Yalçıntürk"]