[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"perceived-stress\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:perceived-stress":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,50,76,106,135,165,201,222,246,273,310],{"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":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":4},"100650725","gardening-activities-stress-and-social-interaction-in-college-students-100650725",false,"NCT07753109","Gardening Activities, Stress, and Social Interaction Among University Students","The Effect of Gardening Activities on Peer Interaction, Stress Levels, and Nature Engagement Behaviors in University Students","Garden-Stress","Inclusion Criteria:\n\n* Being an active undergraduate student at Bingol University Vocational School of Health Services (VSHS)\n* Being between 18 and 25 years of age\n* Providing written informed consent to participate in the study\n* Having no physical disability or chronic illness preventing outdoor physical activity\n* Having no known pollen or soil allergies\n\nExclusion Criteria:\n\n* Absence from more than 25% of the sessions (missing more than 2 sessions) during the intervention\n* Initiating a new professional psychiatric or psychological treatment process during the study period","ALL","18 Months","25 Months",{"count":21,"type":22},100,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study is a quasi-experimental research project with a pretest-posttest control group design, structured to determine the effect of organized gardening activities on peer interaction, stress levels, and nature engagement behaviors among university students.The population of the research consists of students from the Vocational School of Health Services (VSHS) at Bingol University. The sample size, determined via G\\*Power analysis (including a 20% anticipated drop-out rate), comprises a total of 100 volunteer students, divided into an intervention group (n = 50) and a control group (n = 50).The intervention group will participate in a structured program held twice weekly for 1 month (totaling 8 sessions, 60-90 minutes each) in the VSHS garden, encompassing soil preparation, paired seedling planting, group-oriented maintenance, and landscaping activities. The control group will maintain their routine campus life.Data will be collected using a Personal Information Form, the Perceived Self-Efficacy Scale (Coping with Stress), the University Life Scale (Peer Relations Subscale), and the Connectedness to Nature Scale. The data will be evaluated through homogeneity tests and parametric\u002Fnon-parametric comparative analyses (t-tests, Wilcoxon, Mann-Whitney U).Contingency plans (Plan B)-such as indoor potted plant\u002Fterrarium workshops and buffer sample recruitment-are established to address adverse weather conditions, sample attrition, and seasonal risks.",[28,29,30],"Psychosocial Wellbeing","Perceived Stress","Peer Interaction in University Students",[32,33,29,34,35,36,37],"Gardening Activities","Horticultural Therapy","Peer Interaction","Nature Engagement","University Students","Quasi-Experimental Study","NOT_YET_RECRUITING","2026-08-12",{"date":41,"type":42},"2026-08-14","ACTUAL",{"date":44,"type":22},"2026-09-01",{"date":46,"type":22},"2027-01-01",{"name":48,"class":49},"Ataturk University","OTHER",{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":58,"minAge":59,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100648665","mandala-coloring-stress-and-anxiety-100648665","NCT07726186","Mandala Coloring, Stress, and Anxiety","Effects of Mandala Coloring Activity on Perceived Stress and Anxiety in Women With High-Risk Pregnancies","Inclusion Criteria:\n\n* Aged 18 years or older\n* Able to read, write, and communicate in Turkish\n* Singleton pregnancy\n* Hospitalized with a diagnosis of a high-risk pregnancy (e.g., threatened preterm labor, gestational hypertension, mild preeclampsia, gestational diabetes mellitus, intrauterine growth restriction (IUGR), oligohydramnios, stable premature rupture of membranes risk \\[excluding PPROM\\], maternal obesity, etc.)\n* Planned hospitalization of at least 3 days to ensure completion of the intervention\n* Between 20 and 36 weeks of gestation\n\nExclusion Criteria:\n\n* Presence of a fetal anomaly or fetal distress\n* Gestational age below 20 weeks or above 36 weeks\n* Imminent delivery or active labor\n* Communication difficulties (e.g., hearing or visual impairment, or inability to communicate effectively in Turkish)\n* Diagnosis of a psychiatric disorder\n* Previous participation in similar psychosocial or mind-body interventions",true,"FEMALE","18 Years",{"count":61,"type":22},60,[25],"\\*\\*Abstract\\*\\*\n\nAlthough pregnancy is a physiological process, it also involves various risks that may threaten the health of both the mother and fetus. Complications arising in high-risk pregnancies and prolonged bed rest increase stress and anxiety levels in women, negatively affecting both physical and psychological well-being. Failure to recognize or appropriately manage these adverse conditions may lead to serious perinatal outcomes such as preterm birth, low birth weight, depression, and difficulties in mother-infant bonding, thereby creating an additional burden on both maternal-infant health and the healthcare system.\n\nThis proposed project aims to examine the effect of mandala coloring activity on perceived stress and anxiety in women with high-risk pregnancies. The study will be conducted as a randomized controlled experimental study with a pretest-posttest design. The population of the study will consist of pregnant women hospitalized in the Obstetrics and Gynecology service of Kahramanmaraş Sütçü İmam University Health Practice and Research Hospital. Based on power analysis, with a significance level of α = 0.05 and statistical power of (1-β) = 0.80, at least 26 participants per group were required assuming a large effect size (Cohen's d ≈ 0.80). Considering potential sample loss, 30 participants were planned for each group, resulting in a total sample size of 60.\n\nBefore data collection, ethics committee approval and institutional permission will be obtained. Data will be collected using the Personal Information Form, the Perceived Stress Scale in Risky Pregnancies Based on the Neuman Systems Model, and the State Anxiety Inventory. Pregnant women in the experimental group will participate in mandala coloring once daily for three consecutive days. Stress and anxiety levels will be assessed before and after the intervention using the relevant scales. In addition to descriptive statistical methods, appropriate statistical tests will be used according to normality assumptions. The methods specified in the project will be carried out by the principal investigator under the supervision of the advisor.\n\nThe project is expected to demonstrate that mandala coloring is effective in reducing stress and anxiety in women with high-risk pregnancies. In line with the goals emphasized in Türkiye's 12th Development Plan regarding innovative healthcare practices and strengthening public health, the findings are expected to contribute to the protection of maternal and infant health and the promotion of psychological well-being. Furthermore, by supporting reductions in medication use, length of hospital stay, and healthcare costs, the project may contribute to the dissemination of cost-effective, accessible, and holistic care approaches within the healthcare system.\n\nMandala coloring is an easily applicable, side-effect-free, and low-cost method that does not require special equipment, technical expertise, or a professional art therapist. In this respect, it represents a sustainable non-pharmacological intervention that can be easily implemented by nurses in both hospital settings and community-based healthcare services, with almost no training or material costs. Therefore, the findings of this project are expected to support not only individual-level psychological relaxation but also the development of cost-effective, innovative, and accessible care models in healthcare services. The project outcomes are also expected to strengthen the holistic care approach in nursing and promote the integration of non-pharmacological interventions into clinical protocols.\n\nThe findings of the study will be published in scientific journals and presented at national and international congresses. In addition, this research will contribute to the literature and provide a basis for the development of more comprehensive future projects. One of the most important outcomes of this research is that it will enable an undergraduate student to gain experience in conducting research, interpreting results, and preparing for publication, thereby contributing to the training of qualified researchers in priority areas of our country.",[65,29,66],"High-risk Pregnancy","Anxiety","2026-07-20",{"date":69,"type":42},"2026-07-24",{"date":71,"type":22},"2026-08-01",{"date":73,"type":22},"2026-12-30",{"name":75,"class":49},"Kahramanmaras Sutcu Imam University",{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":57,"sex":58,"minAge":84,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":23,"phases":87,"briefSummary":88,"conditions":89,"keywords":97,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":4},"100623836","fascial-yoga-in-menopausal-women-100623836","NCT07401810","Fascial Yoga in Menopausal Women","The Effect of Fascial Yoga on Perceived Stress, Cognitive Control, and Cognitive Flexibility in Menopausal Women","FascialYogaM","Inclusion Criteria:\n\n* Female participants aged 45-65 years\n* In the menopausal period, defined as at least 12 months since the last menstrual period\n* Able to read and understand Turkish and to complete self-report questionnaires\n\nExclusion Criteria:\n\n* Current or past diagnosis of a psychiatric disorder or ongoing psychiatric treatment\n* Regular use of antidepressant, anxiolytic, or corticosteroid medications\n* History of cancer or currently receiving active oncological treatment\n* Participation in fascial yoga, yoga, or similar yoga-based programs within the past 6 months\n* Any medical condition that may prevent safe participation in mild physical activity","45 Years","65 Years",{"count":61,"type":22},[25],"Aim:\n\nThe aim of this study is to evaluate the effects of a structured fascial yoga-based behavioral intervention on perceived stress, cognitive control, and cognitive flexibility in menopausal women. The study aims to determine whether a non-pharmacological and non-invasive behavioral intervention can support psychological and cognitive functioning and reduce perceived stress in menopausal women.\n\nDesign:\n\nThis study is designed as a randomized controlled, pretest-posttest experimental study with a post-intervention follow-up assessment. Eligible participants will be randomly assigned to either the intervention group or the control group receiving usual care. Outcomes will be assessed at baseline, immediately after the intervention, and at follow-up to evaluate both the immediate and sustained effects of the intervention.\n\nMethod:\n\nA total of 60 menopausal women aged 45-65 years will be recruited from the menopause outpatient clinic and randomly assigned to either the intervention group or the control group. The intervention group will participate in a 12-week online fascial yoga program consisting of two 60-minute sessions per week.\n\nIn this study, fascial yoga is defined as a fascia-focused, non-pharmacological, and non-invasive behavioral intervention that includes myofascial release techniques, breath regulation, body awareness, and basic yoga practices to support stress regulation and cognitive functioning. The program will include myofascial release techniques, basic yoga postures suitable for all physical fitness levels, and structured breathing exercises. All sessions will be conducted online in a group format, and no audio or video recordings will be taken.\n\nThe control group will continue to receive routine outpatient care during the study period. After completion of the follow-up assessments, the fascial yoga program will be offered to participants in the control group upon request.\n\nData will be collected at three time points: at baseline before the intervention, immediately after completion of the 12-week intervention, and at the follow-up assessment 8 weeks after the intervention. Perceived stress, cognitive control, and cognitive flexibility will be assessed using validated self-report questionnaires.\n\nHypotheses:\n\nH1: Menopausal women participating in the fascial yoga intervention will show a significant reduction in perceived stress levels compared with the control group at post-intervention and follow-up assessments.\n\nH2: Menopausal women participating in the fascial yoga intervention will show a significant improvement in cognitive control and cognitive flexibility compared with the control group at post-intervention and follow-up assessments.",[90,91,92,93,94,95,29,96],"Menopause","Stress, Psychological","Cognitive Flexibility","Nonpharmacological Interventions","Randomized Controlled Trial","Cognitive Control","Yoga",[90,29,92,95,96],{"date":99,"type":42},"2026-07-22",{"date":101,"type":22},"2026-07-01",{"date":103,"type":22},"2027-06-01",{"name":105,"class":49},"Marmara University",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":110,"acronym":111,"eligibilityCriteria":112,"healthyVolunteers":57,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":113,"targetDuration":115,"studyType":116,"phases":4,"briefSummary":117,"conditions":118,"keywords":4,"overallStatus":124,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":134},"100647364","the-comet-study-a-prospective-cohort-of-medical-residents-to-assess-professional-personal-and-psychological-trajectories-of-residents-in-general-internal-medicine-100647364","NCT07707453","The COMET Study: a Prospective COhort of MEdical residenTs to Assess Professional, Personal and Psychological Trajectories of Residents in General Internal Medicine","COMET","Inclusion Criteria:\n\nResident physician in general internal medicine employed at a participating study site or annex centre during the recruitment period Written informed consent\n\nExclusion Criteria:\n\nNot providing direct patient care Severe mental or physical condition precluding informed consent or compliance with the protocol",{"count":114,"type":22},800,"5 Years","OBSERVATIONAL","Introduction.\n\nSwitzerland, like most Western countries, faces a paradox: an ageing, multimorbid population needs general internal medicine (GIM) physicians more than ever, yet fewer young doctors choose - and stay in - the specialty. Career decisions during residency are intertwined with well-being, mental and physical health, and work-life balance, and distress in training has been associated with depression, burnout, attrition and poorer patient care. Longitudinal data following GIM residents across these domains, and linking them to actual career trajectories, are lacking. The COMET study establishes a multicentre prospective cohort of GIM residents to fill this gap.\n\nMethods and analysis.\n\nCOMET is a prospective, open, multicentre cohort conducted in the departments of (general) internal medicine of Fribourg Hospital (HFR, four sites), Bern University Hospital (Inselspital) and Lausanne University Hospital (CHUV). All GIM residents providing direct patient care are eligible (≈334 residents; expected enrolment ≥267, assuming 80% participation). Participants complete an annual online survey (REDCap; French or German) at baseline and for at least four years, covering sociodemographics; job characteristics; career intentions and 24 factors for or against a GIM career; well-being (Physician Well-Being Index, Professional Fulfillment Index, quality of life, work-life balance); mental health (CES-D, Perceived Stress Scale, Maslach Burnout Inventory, Questionnaire of Cognitive and Affective Empathy); and physical health (step counts, physical activity, fatigue, sleep, healthcare utilisation). Primary endpoints are the longitudinal course of well-being and distress (PWBI, PFI, CES-D) and residents' career trajectory. Analyses combine descriptive statistics, mixed-effects and regression models, and comparisons with the population-based CoLaus\\|PsyCoLaus cohort.",[119,120,121,29,122,123],"Burnout Syndrome","Depression Disorder","Insomnia","Fatigue Symptom","Empathy","RECRUITING","2026-07-15",{"date":127,"type":42},"2026-07-16",{"date":129,"type":42},"2025-08-01",{"date":131,"type":22},"2031-12-31",{"name":133,"class":49},"University of Fribourg",3,{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":4,"eligibilityCriteria":141,"healthyVolunteers":11,"sex":17,"minAge":142,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":116,"phases":4,"briefSummary":146,"conditions":147,"keywords":150,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":164},"100638717","psychological-resilience-perceived-stress-and-periodontal-status-among-bruxers-100638717","NCT07615140","Psychological Resilience, Perceived Stress and Periodontal Status Among Bruxers","Psychological Resilience as a Modifier of the Relationship Between Perceived Stress and Periodontal Status Among Bruxers: a Cross-sectional Study","Inclusion Criteria:\n\n* Patients with age group 30-50 years diagnosed with generalized periodontitis.\n* Probable bruxers (as per BruxScreen questionnaire)\n* Presence of minimum 20 teeth excluding third molars\n* Able to read\u002Funderstand Hindi or English (for questionnaires)\n\nExclusion Criteria:\n\n* Systemic diseases that may affect periodontal disease progression or outcome of treatment (diabetes, autoimmune diseases)\n* History of Periodontal treatment within last 6 months\n* History of Antibiotic use within the previous 3 months\n* History of Steroid, immunosuppressive and psychiatric drug use\n* Pregnant and lactating women\n* Smoking or substance abuse","30 Years","50 Years",{"count":145,"type":22},75,"The present study aims to evaluate psychological resilience as a modifier of the relationship between perceived stress and periodontal status among bruxers. Given that both stress and inflammation share common neuroendocrine and immunological pathways, resilience may play a crucial role in buffering stress-induced periodontal breakdown. Understanding this relationship could shift periodontal management toward a biopsychosocial model, integrating psychological assessment and resilience enhancement with conventional non-surgical therapy. Such insights could help design personalized periodontal care strategies addressing both biological and psychological determinants of disease progression.",[148,149,29],"Periodontitis","Bruxism",[151,152,153,154],"periodontitis","bruxism","stress","resilience","2026-05-30",{"date":157,"type":42},"2026-06-02",{"date":159,"type":22},"2026-06-21",{"date":161,"type":22},"2026-12",{"name":163,"class":49},"Postgraduate Institute of Dental Sciences Rohtak",1,{"id":166,"slug":167,"hasResults":11,"nctId":168,"briefTitle":169,"officialTitle":170,"acronym":171,"eligibilityCriteria":172,"healthyVolunteers":11,"sex":17,"minAge":173,"maxAge":4,"enrollmentInfo":174,"targetDuration":4,"studyType":23,"phases":176,"briefSummary":177,"conditions":178,"keywords":187,"overallStatus":124,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":197,"leadSponsor":199,"locationsCount":164},"100595769","enjoying-affordable-and-tasty-food-together-100595769","NCT07036757","Enjoying Affordable and Tasty Food Together","PROJECT EATT: Enjoying Affordable and Tasty Food Together","PROJECT EATT","Inclusion Criteria:\n\n* Adults aged 40 years and older.\n* Household income at or less than the 200% the federal poverty level (household size 1: $30,120, household size 2: $40,880, household size 3: $51,640, household size 4: $62,400, and household size 5: $73,160)\n* Willing to provide informed consent and complete the study requirements, including attending study visits and completing questionnaires.\n* Access to a refrigerator or other means to safely store perishable food, as the meal kits require refrigeration.\n* BMI \\> 30 kg\u002Fm2 and self-report having at least one of the following: elevated blood pressure or hypertension, elevated glucose, prediabetes or diabetes.\n* Reside in the Greater Lowell area or surrounding regions to ensure feasibility of meal kit delivery and data collection.\n\nExclusion Criteria:\n\n* Less than 40 years old\n* Does not have BMI \\>30 kg\u002Fm2, elevated blood pressure or hypertension, or elevated glucose, prediabetes or diabetes\n* Not able to provide consent (adults lacking capacity)\n* Follow a medically restricted diet or have allergies to wheat, soy, or dairy\n* Plans to move from the Greater Lowell area within the next 12 months\n* Live outside the Greater Lowell area because this will impact meal kit delivery\n* Individuals without a working refrigerator in your household\n* Have a serious medical condition requiring a doctor's care including cancer, chronic kidney disease and\u002For celiac disease\n* Currently part of a study on diabetes, cardiovascular disease, nutrition or weight-loss\n* Currently taking any weight loss medication like Ozempic, or medication for diabetes, dyslipidemia or hypertension\n* Currently using a continuous glucose monitor","40 Years",{"count":175,"type":22},120,[25],"The goal of this pilot study is to examine the feasibility of a novel meal kit and nutrition education intervention among adults aged 40 years and older, who are lower income, and to evaluate the preliminary impact of the meal kit and nutrition education intervention on food insecurity, dietary quality, mental health, quality of life and cardiovascular risk factors compared with general nutrition education materials in this population.\n\nThe main questions are:\n\nWhat is the acceptability and satisfaction with the meal kits and nutrition education intervention?\n\nWhat are the participation rates in the nutrition education program and the evaluation of the intervention?\n\nWhat is the impact of the intervention on food insecurity, dietary quality and cooking and food preparation self-efficacy compared with general nutrition education materials?\n\nWhat is the impact of the intervention of psychosocial health, quality of life and cardiometabolic outcomes compared with general nutrition education materials?",[179,180,181,182,29,66,183,184,185,186],"Food Insecurity","Dietary Quality","Quality of Life","Cooking Self-efficacy","Depressive Symptomatology","Anthropometrics: Height and Weight","Glucose Variability","Blood Pressure",[188,189,190,191,181],"Nutrition Education","Cardiometabolic outcomes","Meal Kits","Stress and Mental Health","2026-04-28",{"date":194,"type":42},"2026-05-05",{"date":196,"type":42},"2026-02-01",{"date":198,"type":22},"2026-10-30",{"name":200,"class":49},"University of Massachusetts, Lowell",{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":205,"acronym":4,"eligibilityCriteria":206,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":4,"enrollmentInfo":207,"targetDuration":4,"studyType":23,"phases":209,"briefSummary":210,"conditions":211,"keywords":4,"overallStatus":124,"whyStopped":4,"lastUpdateSubmitDate":214,"lastUpdatePostDateStruct":215,"startDateStruct":217,"completionDateStruct":218,"leadSponsor":220,"locationsCount":164},"100615854","a-pilot-study-of-rise-for-nurse-managers-retreat-100615854","NCT07298018","A Pilot Study of RISE for Nurse Managers Retreat","Inclusion Criteria:\n\n* an employed AdventHealth Nurse Manager\n* a \"moderate\" or \"high\" score in burnout equal to ≥17 in the Emotional Exhaustion Domain and\u002For ≥7 in the Depersonalization Domain on the MBI\n\nExclusion Criteria:\n\n* a direct care RN, Nurse Director, Educator, and Executive\n* a \"low\" score in burnout equal to \\\u003C17 in the Emotional Exhaustion domain and\u002For \\\u003C7 in the Depersonalization domain on the MBI",{"count":208,"type":22},16,[25],"The purpose of this study is to determine the feasibility and acceptability of the RISE for Nurse Managers retreat and its impact on occupational and psychological well-being indicators",[212,213,29],"Burnout","Secondary Traumatic Stress","2026-02-17",{"date":216,"type":42},"2026-02-19",{"date":196,"type":22},{"date":219,"type":22},"2026-12-16",{"name":221,"class":49},"AdventHealth",{"id":223,"slug":224,"hasResults":11,"nctId":225,"briefTitle":226,"officialTitle":226,"acronym":4,"eligibilityCriteria":227,"healthyVolunteers":57,"sex":17,"minAge":59,"maxAge":142,"enrollmentInfo":228,"targetDuration":4,"studyType":23,"phases":230,"briefSummary":231,"conditions":232,"keywords":4,"overallStatus":124,"whyStopped":4,"lastUpdateSubmitDate":237,"lastUpdatePostDateStruct":238,"startDateStruct":240,"completionDateStruct":242,"leadSponsor":244,"locationsCount":164},"100618572","efficacy-of-interactive-audio-based-mindfulness-chatgpt-powered-intervention-on-well-being-100618572","NCT07333365","Efficacy of Interactive Audio-based Mindfulness ChatGPT-Powered Intervention on Well-being","Inclusion Criteria:\n\n* Participants who are aged 18 to 30 (inclusive)\n\nExclusion Criteria:\n\n* Not applicable",{"count":229,"type":22},210,[25],"Brief mindfulness intervention is a short form is a form of short-duration practice, typically delivered for around 30 minutes or less (Howarth et al., 2019). It can be conducted in various formats, including a short breathing exercise or body scan (Palascha et al., 2021), and are increasingly offered through digital platforms, including app-based formats.\n\nEmpirical evidence has examined the efficacy of brief mindfulness intervention and yielded mixed results. For some studies, positive effects were found, while some studies found no supporting evidence. Such inconsistencies may be due to the several current limitations of brief mindfulness intervention. Firstly, the duration of the intervention is too short. Given this brevity, these short practices may not offer the same immersion and depth that traditional mindfulness may offer. Secondly, most brief mindfulness utilised audio-based formats, which tend to be passive in nature and may not fully engage participants. Lastly, for brief mindfulness delivered through app-based platforms, these applications adopt a self-help approach, which may lower engagement and user commitment. Moreover, these applications also relied on audio guides which lacks the student-facilitator engagement found in traditional classes.\n\nTo address the current limitations within the literature, a between-within-subjects experiment will be conducted where participants will be randomly assigned to one of the three conditions: (1) an interactive brief mindfulness breathing ChatGPT-powered intervention, (2) an interactive mind-wandering ChatGPT-powered control, or (3) a mindfulness breathing audio control. We hypothesise that the brief mindfulness breathing ChatGPT-powered intervention group will have significant improvements in well-being outcomes as compared to the other two control groups. By exploring the potential of an interactive ChatGPT-powered intervention, this study aims to understand its efficacy in improving well-being.",[29,233,234,235,236],"Positive and Negative Affect","State Anxiety","Self Control","State Mindfulness Attention","2025-12-30",{"date":239,"type":42},"2026-01-12",{"date":241,"type":42},"2025-10-30",{"date":243,"type":22},"2026-05",{"name":245,"class":49},"Singapore Management University",{"id":247,"slug":248,"hasResults":11,"nctId":249,"briefTitle":250,"officialTitle":250,"acronym":4,"eligibilityCriteria":251,"healthyVolunteers":57,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":252,"targetDuration":4,"studyType":23,"phases":254,"briefSummary":255,"conditions":256,"keywords":257,"overallStatus":124,"whyStopped":4,"lastUpdateSubmitDate":263,"lastUpdatePostDateStruct":264,"startDateStruct":266,"completionDateStruct":268,"leadSponsor":270,"locationsCount":272},"100606903","resilience-enhancement-training-program-to-confront-nursing-students-perceived-stress-100606903","NCT07181603","Resilience Enhancement Training Program to Confront Nursing Students' Perceived Stress","Inclusion Criteria:\n\n* Nursing students enrolled in the Psychiatric and Mental Health Nursing (PMHN) course at the Faculty of Nursing, Ain Shams University during the first semester of the academic year 2025-2026.\n* Willing to participate and able to provide informed consent\n\nExclusion Criteria:\n\n* Students who decline participation or withdraw consent at any time.\n* Students absent for the majority of the program sessions.",{"count":253,"type":22},90,[25],"The goal of this clinical trial is to assess if a resilience enhancement training program can help nursing students manage stress more effectively. The main question it aims to answer is:\n\nDoes the program improve nursing students' resilience levels?\n\nDoes the program lower nursing students' perceived stress levels?\n\nResearchers will compare students who receive the training during the semester with students who do not receive it until after the study is completed to see if the training has an effect.\n\nParticipants will:\n\n1. Complete questionnaires on resilience and stress before and after the training.\n2. Attend a structured resilience enhancement training program for 10 weeks alongside their usual studies.\n3. Be part of either the study group (receiving the training first) or the comparison group (receiving the training after study completion).",[29],[258,259,260,261,262],"Resilience","Perceived stress","Stress management","Nursing students","Resilience training program","2025-11-13",{"date":265,"type":42},"2025-11-17",{"date":267,"type":42},"2025-11-02",{"date":269,"type":22},"2026-01",{"name":271,"class":49},"Ain Shams University",2,{"id":274,"slug":275,"hasResults":11,"nctId":276,"briefTitle":277,"officialTitle":278,"acronym":279,"eligibilityCriteria":280,"healthyVolunteers":57,"sex":17,"minAge":281,"maxAge":4,"enrollmentInfo":282,"targetDuration":4,"studyType":23,"phases":284,"briefSummary":285,"conditions":286,"keywords":290,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":302,"startDateStruct":304,"completionDateStruct":306,"leadSponsor":308,"locationsCount":4},"100601529","evaluation-of-the-school-based-sim-program-in-upper-secondary-school-students-100601529","NCT07111676","Evaluation of the School-based SIM Program in Upper Secondary School Students","Evaluating the Efficacy and Cost-effectiveness of the School-based Solution-focused Intervention for Mental Health (SIM) in First Year of Upper Secondary School Students","SIMRCT1","Inclusion Criteria:\n\n* first and second-year upper secondary school students\n* students enrolled in regular school programs\n\nExclusion Criteria:\n\n* students with insufficient knowledge of the Swedish language\n* students who are absent during the information meeting or could not be reached for a separate meeting to receive the accurate information\n* students who are absent at the start session or cannot be reached to complete the baseline prior to the first themed SIM session\n* students who for various reasons (e.g. functional impairments) are unable to participate in an ordinary teaching situation.","15 Years",{"count":283,"type":22},560,[25],"Söderqvist et al. recently reported on a new school-based program designed to promote mental well-being in adolescents: the Solution-Focused Intervention for Mental Health (SIM, https:\u002F\u002Fdoi.org\u002F10.1016\u002Fj.ssmmh.2025.100493). While previous studies on SIM were designed mainly to test, develop, refine and improve the program and its feasibility in a school setting, the current project aims to test the efficacy of SIM on adolescent mental health, primarily mental well-being.\n\nA two-arm, cluster, randomized, controlled trial will be conducted. The intervention group will receive the SIM program, and the control group will receive a lecture on mental well-being along with the usual school provisions. Randomization is done by class because the intervention takes place in mentor groups. Based on the results of our largest feasibility study, 559 students are required for paired measurements to detect a small effect on mental well-being with 80% power and a significance level of 0.05. The evaluation is based on validated instruments, with measurements taken before and after the intervention, as well as six and nine months later. The project is being implemented in collaboration with six upper secondary schools in Sweden. Recruitment and anchoring at the participating schools, as well as class randomization strafied on educational program, took place in 2025. Enrollment of participating students will begin in January 2026.\n\nThis project will contribute new knowledge to the field by evaluating a universal program for schools to use in their health promotion work. The latter is important since high levels of mental well-being independently predict a lower incidence of subsequent mental illness and have a range of positive effects on individuals and society.",[287,288,289,29],"Solution-focused Capability","Mental Well-being","Mental Problems",[291,292,293,294,295,296,297,298,299,300,301],"Mental well-being","Solution-focused Intervention for mental health","SIM","School-based intervention","Strength-based","Mental health promotion","Solution-focused coaching","Cluster randomized controlled trial","Adolescents","Solution-focused brief therapy","Universal mental health intervention",{"date":303,"type":42},"2025-08-08",{"date":305,"type":22},"2026-12-01",{"date":307,"type":22},"2027-10",{"name":309,"class":49},"Region Örebro County",{"id":311,"slug":312,"hasResults":11,"nctId":313,"briefTitle":314,"officialTitle":315,"acronym":316,"eligibilityCriteria":317,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":4,"enrollmentInfo":318,"targetDuration":4,"studyType":23,"phases":320,"briefSummary":321,"conditions":322,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":327,"lastUpdatePostDateStruct":328,"startDateStruct":330,"completionDateStruct":332,"leadSponsor":334,"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":319,"type":22},80,[25],"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.",[323,324,29,325,326],"Alzheimer Disease","Caregivers of Alzheimer's Disease or Memory Problem Patients","Well-Being (Psychological Flourishing)","Care Burden","2024-12-24",{"date":329,"type":42},"2025-01-01",{"date":331,"type":22},"2025-02-15",{"date":333,"type":22},"2025-08-15",{"name":335,"class":49},"Aydan Akkurt Yalçıntürk"]