[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"mental-health-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:mental-health-care":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,49,80,111,154,182,216,241],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100637411","cansolve-20-theme-31-mind-the-gap---dialectical-behavioural-therapy-dbt-skills-training-program-pilot-100637411",false,"NCT07628309","CanSOLVE 2.0 Theme 3.1 Mind the Gap - Dialectical Behavioural Therapy (DBT) Skills Training Program Pilot","CanSOLVE 2.0 Theme 3.1 Mind the Gap: Addressing Mental Health Care Gaps for Canadians Receiving Facility-Based Hemodialysis - Dialectical Behavioural Therapy (DBT) Skills Training Program Pilot Intervention","Inclusion Criteria:\n\n* Age \\> 18 years old\n* Individuals followed in the Manitoba Kidney Health Program at Seven Oaks General Hospital or Health Sciences Centre sites with advanced chronic kidney disease not yet on facility-based hemodialysis but with plans to start within 1 month; OR\n* Individuals followed in the Manitoba Kidney Health Program at the SOGH or HSC sites who have initiated facility-based hemodialysis within the last 90 days\n* Able and willing to attend weekly DBT sessions (either virtually or in-person)\n* Experiencing self-reported psychological distress related to advanced kidney disease or initiation of hemodialysis\n* Deemed eligible to participate by study clinical psychologist\n\nExclusion Criteria:\n\n* Unable to complete intervention due to planned relocation\u002Ftransplant\u002Fmodality change\n* Unable to communicate in English\n* Deemed by hemodialysis unit staff\u002Fphysician\u002Fstudy psychologist to be unable to participate fully in study activities due to:\n\n  * Actively participating in psychiatric care with psychiatric (DSM-5) diagnosis\n  * Requiring referral for psychiatric care as per facility-based HD care provider assessment\n  * Current psychotic symptoms\n  * Cognitive impairment that would limit ability to participate in group or complete homework\n  * Safety risk to staff (e.g. physical aggression)\n  * Antisocial personality disorder or other issues that may limit ability to constructively participate in peer group\n  * Severe comorbid substance use disorder (if present will offer referral to addictions resources or Addictions Psychiatry)","ALL","18 Years",{"count":19,"type":20},35,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this pilot implementation study is to implement and evaluate a 13-week dialectical behavioural therapy (DBT) skills training program to address challenges to mental health and mental wellbeing in people who have recently started facility-based hemodialysis or those who may start within the next 6-12 months.",[26,27,28,29,30],"Mental Health","Mental Health Care","Hemodialysis","DIALYSIS SYMPTOMS AND ANXIETY","Health Related Quality of Life",[32,33,34,35],"hemodialysis","mental health","dialysis anxiety","mental well-being","RECRUITING","2026-05-29",{"date":39,"type":40},"2026-06-05","ACTUAL",{"date":42,"type":40},"2026-03-05",{"date":44,"type":20},"2026-07-15",{"name":46,"class":47},"University of Manitoba","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":16,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":21,"phases":62,"briefSummary":63,"conditions":64,"keywords":66,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":48},"100609798","mental-health-cpr-for-cancer-survivors-100609798","NCT07219264","Mental Health CPR for Cancer Survivors","Mental Health CPR: Transforming Cancer Survivors' Mental Health With Community Participatory Reach","MH-CPR CaS","The study will include adults of all ages representing individuals across all the adulthood stage. The minimum age requirement is 21, which is the legal age of majority in Puerto Rico.\n\nInclusion Criteria:\n\n* Eligibility Criteria for Sub-Aim 1a. The eligibility criteria for the qualitative interviews will be 1: Participants over 21 years old, 2: through their role or status, represent any of the following community sectors: cancer care community organization representatives, clinical care providers of cancer patients and survivors, and cancer health educators; 3: self-identified as a Latino\u002FHispanic; 4: be able to complete an interview.\n* Eligibility Criteria for Aim 2. Community Forums stakeholders eligibility criteria. The community stakeholders inclusion criteria for the community forum are 1: Participants over 21 years old, 2: through their role or status, represent any of the following community sectors: cancer patients\u002Fsurvivors, cancer patients\u002Fsurvivors identified family caregiver, healthcare providers, cancer supportive care organizations, and advocacy groups, 3: self-identified as a Latino\u002FHispanic, 4: be able to attend the community forums.\n* Community Leaders Eligibility Criteria for CMHW training. The inclusion criteria for the community leaders to be trained as CMHW are 1: Participants over 21 years of age, 2: living in a limited resource community in southern Puerto Rico, 3: self-identified as a Latino\u002FHispanic, and 4: be able to provide support to H-CAPS through their role as CMHW.\n* Communities Eligibility Criteria. Community municipalities included from the southern health region of Puerto Rico are: Ponce, Arroyo, Coamo, Yauco, Salinas, Guanica, Guayanilla, Juana Diaz, Adjuntas, Guayama, Patillas, Santa Isabel, Penuelas and Villalba. These municipalities were chosen because they represent the catchment area of Ponce Health Sciences University.\n\nAlso, they are comprised of mostly rural areas (south-central region of Puerto Rico) and present a higher incidence of cancer (south region) and cancer mortality (south-central region) compared to other Puerto Rican Health regions.\n\n* Intervention eligibility criteria. The eligibility criteria for the community intervention are 1: Participants over 21 years old, 2: living in any of the municipalities of the southern health region of Puerto Rico and within a limited resource community according to the CDC SVI, 3: self-identified as a Latino\u002FHispanic, and 4: have had a cancer diagnosis during their adulthood.\n\nExclusion Criteria:\n\n* Participants residing outside the catchment area.",true,"21 Years","99 Years",{"count":61,"type":20},1260,[23],"This is a parallel, two-arm interventional study comparing the Mental Health CPR behavioral intervention to standard community health education. The goal of this clinical trial is to learn if Mental Health CPR program, a culturally and linguistically adapted behavioral intervention, helps improve emotional well-being and access to mental health services among Hispanic\u002FLatino cancer survivors in Puerto Rico.\n\nThe main questions it aims to answer are:\n\n* Does Mental Health CPR help more people complete psychological distress screening?\n* Does it help more participants connect with psycho-oncology services? Researchers will compare the Mental Health CPR program to standard community health education to determine whether it improves emotional well-being, enhances communication between patients and caregivers, reduces negative attitudes toward mental health care, and lowers emotional distress levels.\n\nParticipants will:\n\n* Attend community sessions led by trained Community Mental Health Workers (CMHWs)\n* Receive printed materials and educational resources\n* Take part in brief follow-ups over about 36 weeks",[27,26,65],"Depression Anxiety Disorder",[26,67,68,69],"Distress","Depression","Anxiety","2025-10-17",{"date":72,"type":40},"2025-10-21",{"date":74,"type":40},"2025-09-26",{"date":76,"type":20},"2028-08-31",{"name":78,"class":79},"Ponce Medical School Foundation, Inc.","INDUSTRY",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":90,"phases":4,"briefSummary":91,"conditions":92,"keywords":93,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":48},"100453241","evaluation-of-a-flexible-and-integrative-psychiatric-care-model-at-the-pfalzklinikum-evapfalz-100453241","NCT05181982","Evaluation of a Flexible and Integrative Psychiatric Care Model at the Pfalzklinikum (EVA_Pfalz)","Wissenschaftliche Evaluation Des Modellvorhabens (§ 64b SGB V) am Pfalzklinikum (EVA_Pfalz)","EVA_Pfalz","Inclusion Criteria:\n\n* treatment at the Pfalzklinikum or control hospital after 01.01.2020 (date included) and before 31.12.2023 (date included) with one of the following diagnoses as main diagnosis (ICD-10: F00, F01, F02, F03, F07, F10, F20-29, F30-39, F43, F45, F40-48, F50, F60.31, F70-79, F84, F90-F98, B22 \\& F02.8, G20.0 \\& F02.3, G30.0 \\& F00.0, G30.1 \\& F00.1) at the department of psychiatry (FA 29xx), department of child and adolescent psychiatry (F30xx) or department of psychosomatic\u002Fpsychotherapy (FA31xx)\n* being insured with any of the participating SHI funds\n\nExclusion Criteria:\n\n* less than one year follow-up data available\n* non-permanent residence in Germany during observation period",{"count":89,"type":20},10000,"OBSERVATIONAL","This study is an evaluation of the flexible and integrative psychiatric care model (according to § 64b of the German Social Code Book V (SGB V)) (FIT) at the Pfalzklinikum. The central concern of this evaluation is to answer the question whether the FIT model offer advantages over standard care. The orientation of model care is a more cross-sectoral provision of services through more flexible treatment intensities.",[27],[94,95,96,97,98,99,100,101],"Cross-sectoral Treatment","Flexible and Integrated Treatment","Global Treatment Budget","FIT","Psychiatry","Evaluation","Claims data","Cohort study","2025-08-19",{"date":104,"type":40},"2025-08-24",{"date":106,"type":40},"2022-09-30",{"date":108,"type":20},"2026-07",{"name":110,"class":47},"Technische Universität Dresden",{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":115,"acronym":116,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":16,"minAge":118,"maxAge":119,"enrollmentInfo":120,"targetDuration":4,"studyType":21,"phases":122,"briefSummary":123,"conditions":124,"keywords":133,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":145,"lastUpdatePostDateStruct":146,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":152,"locationsCount":48},"100584194","my-avenue-to-help---adaptive-mentalization-based-integrative-treatment-compared-to-management-as-usual-for-youths-with-multiple-problems-a-non-randomized-controlled-feasibility-trial-100584194","NCT06886165","My Avenue to helP - Adaptive Mentalization-based Integrative Treatment Compared to Management as Usual for Youths With Multiple Problems: a Non-Randomized Controlled Feasibility Trial","MAP","Inclusion Criteria:\n\n* Criterium A) Documented record of multiple problems defined as at least 2 of the following: (i) Absence from school \u002F non-adherence to education (ii) Risk behaviors like alcohol or cannabis abuse, or repeated suicide attempts or self-harm requiring somatic treatment.(iii) Repeated visits at emergency-, trauma-, or acute wards. And\u002For one of the following: (iv) Contact with police or legal justice system. (v) Homelessness within the last year.\n* Criterium B) Age 12-17 years at time of inclusion.\n* Criterium C) Strong indication of mental disorders defined as a diagnosis of a mental disorder. The type of mental disorders will be further substantiated using the DAWBA after recruitment (Goodman et al., 2000).\n* Criterium D) Written\u002Fsigned informed consent from all legal guardians (in most cases both parents) and oral consent from youths aged 15 years and older. Written\u002Fsigned informed consent from the youths themselves will be collected when they turn 18 if they do so during the study period.\n\nExclusion Criteria:\n\n* Indications of substantial intellectual disability corresponding to IQ below 50, or a level of daily and social functions that do not enable participation in research (e.g., if the young person is not deemed to have the capacity to understand the implications of the study and provide oral consent).\n* Not living in Region Zealand.","12 Years","17 Years",{"count":121,"type":20},60,[23],"My Avenue to HelP (MAP) is a non-randomized feasibility study testing the implementation of a cross-sectoral collaboration targeted youths, aged 12-17 years, with multiple social and psychological problems. MAP is a one-year intervention based on Adaptive Mentalization-Based Integrative Treatment (AMBIT). MAP is not a new treatment method, but rather a new way of offering and organizing support in the existing network around the young person. The objective is to create a new way for professionals across sectors to collaborate in supporting our most vulnerable youth. Thereby, the investigators aim to benefit the youths by incorporating a mentalizing stance to promote lasting changes beyond the intervention period. The MAP Project will run from 2025 to 2027.\n\nThe research will consist of two work packages (WPs)\n\n* WP1 will test the feasibility of the MAP project examining a) whether young people can be successfully recruited to the project b) if the evaluation design and methods are feasible and c) if the intervention is feasible to participants and employees (quantitatively).\n* WP2 will assess implementation determinants and evaluate the implementation strategies employed in the project. Furthermore, the acceptability of the intervention will qualitatively be assessed by interviews with selected participants, their parents, as well as employees.\n\nParticipants:\n\nIn total 60 youths aged 12-17 years from Region Zealand, Denmark:\n\n* 40 youths will be enrolled and receive the one-year MAP Intervention; 30 youths residing in Roskilde Municipality and 10 residing in Lejre Municipality\n* 20 youths from other municipalities in Region Zealand will be included in the trial as a control group.\n\nTo assess the nature and extent of the mental health problems and potential psychiatric disorders among the participating youths, the parents and the young person will be asked to complete an online questionnaire (Development and Well-Being Assessment (DAWBA)).",[27,125,126,127,128,129,130,131,132],"AMBIT","Adaptive Mentalization-Based Integrative Treatment","Child and Adolescent Psychiatry","Health Care Professionals","Mental Health Services","Community Mental Health Services","Emergency Services, Psychiatric","Social Work, Psychiatric",[125,134,127,135,136,137,138,139,140,141,142,143,144],"Adative Mentalization-Based Integrative Treatment","Cross-sectoral Collaboration","Interdisiplinary Collaboration","Implementation","Municipalities","Mentalization","Social Functioning","CAMHS","Feasibility Study","Primary Health Care","Child and Adolescent Mental Health Services","2025-08-06",{"date":147,"type":40},"2025-08-11",{"date":149,"type":40},"2025-03-25",{"date":151,"type":20},"2028-01-31",{"name":153,"class":47},"Pia Jeppesen",{"id":155,"slug":156,"hasResults":11,"nctId":157,"briefTitle":158,"officialTitle":159,"acronym":4,"eligibilityCriteria":160,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":161,"enrollmentInfo":162,"targetDuration":4,"studyType":21,"phases":164,"briefSummary":165,"conditions":166,"keywords":168,"overallStatus":172,"whyStopped":4,"lastUpdateSubmitDate":173,"lastUpdatePostDateStruct":174,"startDateStruct":176,"completionDateStruct":178,"leadSponsor":180,"locationsCount":48},"100596812","evaluation-of-the-specialized-clinic-for-nutrition-and-mental-health-a-pilot-study-100596812","NCT07050342","Evaluation of the Specialized Clinic for Nutrition and Mental Health: A Pilot Study","Evaluation Der Spezialambulanz Ernährung Und Psyche: Eine Pilotstudie","Inclusion Criteria:\n\n* Inclusion Criteria:\n\nNew patient at the outpatient clinic for Nutrition and Psychosomatics\n\nAge between 18 and 65 years\n\nSufficient German language skills\n\nProvided written informed consent\n\nAble and willing to complete online questionnaires via email\n\nExclusion Criteria:\n\n* Lack of consent or inability to provide informed consent\n\nDiagnosed dementia (Mini-Mental State Exam \\\u003C 20)\n\nSevere substance dependence (e.g., alcohol, benzodiazepines, opioids)\n\nSerious physical, neurological, or motor impairments preventing questionnaire completion\n\nNo access to or ability to use email for online forms\n\nDiagnosis of cancer, severe autoimmune disease, or immunosuppression","65 Years",{"count":163,"type":20},84,[23],"The goal of this observational pilot study is to learn how personalized nutrition-focused care can help people with mental and psychosomatic health problems. This study takes place in Europe's first outpatient clinic that focuses on how diet affects mental well-being.\n\nThe main questions the study aims to answer are:\n\nDoes care at this clinic help lower participants' stress levels over one year?\n\nDo participants report better mental health, resilience, and quality of life during the study?\n\nAre improvements in mental health linked to changes in diet and blood markers like inflammation?\n\nParticipants will:\n\nFill out online questionnaires every 3 months over one year. These ask about stress, physical symptoms, quality of life, diet, and satisfaction with care.\n\nGive small blood samples during their regular clinic visits. These samples will be checked for common health markers such as inflammation.\n\nThis study will help researchers understand whether nutrition-focused care can support mental and physical health, and whether this approach should be tested in larger future studies.",[167,27],"Psychosomatic Disorders",[169,167,170,171,26],"Nutritional Psychiatry","Stress Reduction","Personalized Nutrition","NOT_YET_RECRUITING","2025-06-24",{"date":175,"type":40},"2025-07-03",{"date":177,"type":20},"2025-12-01",{"date":179,"type":20},"2028-12-01",{"name":181,"class":47},"Medical University of Graz",{"id":183,"slug":184,"hasResults":11,"nctId":185,"briefTitle":186,"officialTitle":186,"acronym":187,"eligibilityCriteria":188,"healthyVolunteers":57,"sex":189,"minAge":190,"maxAge":190,"enrollmentInfo":191,"targetDuration":4,"studyType":21,"phases":193,"briefSummary":194,"conditions":195,"keywords":198,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":207,"lastUpdatePostDateStruct":208,"startDateStruct":210,"completionDateStruct":212,"leadSponsor":214,"locationsCount":48},"100593631","self-efficacy-and-knowledge-seek-trial-to-improve-sexual-reproductive-health-and-well-being-for-syrian-refugee-women-and-girls-in-lebanon-100593631","NCT07008950","Self-efficacy and Knowledge (SEEK) Trial to Improve Sexual Reproductive Health and Well-being for Syrian Refugee Women and Girls in Lebanon","SEEK","Inclusion Criteria:\n\n\\-\n\nThe target population of the study are Syrian adolescent girls and young women refugees (age 15-24 years) residing in Beqaa governorate in Lebanon. Participants will be included in the study if they meet the following inclusion criteria:\n\n1. are currently married and between the ages of 15 - 24 years,\n2. completed an average stay in Lebanon for a minimum of 6 months,\n3. are willing to take part in the study as indicated by them signing an informed consent (for young women 18 years of age or older) or through a legal guardian consent form and written assent for adolescents' girls between 15 and 17,\n4. have none of the exclusion criteria listed below upon screening.\n\nExclusion Criteria:\n\nParticipants will be excluded from the study if they meet any of the following criteria:\n\n1. are currently pregnant and\u002For lactating,\n2. have reported chronic health problems interfering with the ability to follow the intervention protocol,\n3. have high levels of anxiety and\u002For depression as well as suicidal ideations and\u002For attempts upon screening and\u002For a current diagnosis of a severe mental illness, or undergoing mental health treatment.\n\n   \\-","FEMALE","15 Years",{"count":192,"type":20},485,[23],"This community-based randomized controlled trial (RCT) aims to evaluate a low-resource\u002Flow-intensity integrated sexual reproductive health (SRH) and wellbeing intervention package. It will be delivered in Primary Healthcare Centres (PHCs) in a rural area in Lebanon to Syrian refugee women and girls aged 15-24.",[27,196,197],"Sexual Health Quality of Life","Family Planning Services",[199,200,201,202,203,204,205,206],"sexual health","reproductive health","psychosocial support","wellbeing","RCT","Lebanon","Refugees","Girls and young women","2025-06-05",{"date":209,"type":40},"2025-06-06",{"date":211,"type":40},"2024-01-01",{"date":213,"type":20},"2025-06-30",{"name":215,"class":47},"American University of Beirut Medical Center",{"id":217,"slug":218,"hasResults":11,"nctId":219,"briefTitle":220,"officialTitle":221,"acronym":4,"eligibilityCriteria":222,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":223,"targetDuration":4,"studyType":21,"phases":225,"briefSummary":226,"conditions":227,"keywords":230,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":233,"lastUpdatePostDateStruct":234,"startDateStruct":236,"completionDateStruct":238,"leadSponsor":240,"locationsCount":48},"100566178","feasibility-and-acceptability-of-group-medical-visits-for-anxiety-and-depression-100566178","NCT06651801","Feasibility and Acceptability of Group Medical Visits for Anxiety and Depression","A Pilot Randomized Controlled Trial Assessing the Feasibility and Acceptability of Group Medical Visits for Anxiety and Depression","Inclusion Criteria:\n\n* Adult Central Intake patients (patients referred for psychiatric consultation by their primary care provider) whose primary mental health issue is an anxiety disorder (social anxiety, generalized anxiety, or panic disorder) or depression (major depressive disorder or persistent depressive disorder)\n* Able to participate in English language group with up to 10 participants\n* Able to commit to a virtual biweekly group for about 1.5 hours each group\n* Able to do virtual group from a private location with camera access\n* Live in community in Manitoba and plan to stay for 6-month period\n\nExclusion Criteria:\n\n* Patients with Bipolar 1 or 2 Disorder (even if current episode depression)\n* Primary diagnosis of a personality disorder leading to anxiety\u002Fdepression symptoms (personality disorder traits are not an exclusion criteria)\n* Patients who already have established longitudinal care with a psychiatrist\n* Received ECT treatment within past 6 months\n* Any diagnosis that would significantly impact ability to participate in the group. For example:\n* Moderate-to-severe substance use disorders (in particular substance use throughout day or inability to attend group without using substances before)\n* Current psychotic symptoms\n* Moderate-to-severe intellectual disability or neurocognitive disorder\n* Current significant eating disorder symptoms (for example resulting in significant weight loss\u002Fmalnutrition or that take up a significant part of the day either mentally or physically)\n* Self harm behaviour requiring medical\u002Fpsychiatric attention or active suicidal ideation\u002Fsuicide attempts within the past 6 months\n* Concern about safety of other group members\u002Ffacilitators if this patient were to join",{"count":224,"type":20},20,[23],"The goal of this clinical trial is to evaluate the feasibility and acceptability of the intervention, Group Medical Visits (GMVs), for patients with depression and anxiety. It also aims to get some initial information on the effectiveness of GMVs on reducing depression and anxiety scores, which will help inform power calculations for a future larger randomized controlled trial (RCT). The main question it aims to answer is:\n\n* Are GMVs feasible and acceptable to patients with depression and anxiety?\n\nThis study consists of a pilot RCT with an intervention and control arm. At enrollment, participants will be randomized to the intervention group, 6 months of GMVs, or to the control group, which consists of \"standard client services\". For the GMV group, participants will engage in a biweekly virtual group that is similar to a standard psychiatric follow-up. Participants in the control group will receive standard care after a psychiatric assessment, which includes follow-up with their primary care provider (family physician or nurse practitioner), individual psychiatric care if suggested by the psychiatrist who did their psychiatric assessment, and\u002For a referral to publicly funded therapy groups if interested.",[27,228,229],"Anxiety and Depression","Pilot Study",[231,69,68,232,229],"Group Medical Visits","Shared Medical Appointments","2025-05-09",{"date":235,"type":40},"2025-05-13",{"date":237,"type":40},"2025-04-15",{"date":239,"type":20},"2025-11",{"name":46,"class":47},{"id":242,"slug":243,"hasResults":11,"nctId":244,"briefTitle":245,"officialTitle":246,"acronym":247,"eligibilityCriteria":248,"healthyVolunteers":57,"sex":16,"minAge":17,"maxAge":249,"enrollmentInfo":250,"targetDuration":4,"studyType":21,"phases":252,"briefSummary":253,"conditions":254,"keywords":258,"overallStatus":172,"whyStopped":4,"lastUpdateSubmitDate":263,"lastUpdatePostDateStruct":264,"startDateStruct":266,"completionDateStruct":267,"leadSponsor":269,"locationsCount":48},"100581177","hiit-vs-snack-exercises-on-the-academic-stress-of-university-students-100581177","NCT06846918","HIIT Vs Snack Exercises on the Academic Stress of University Students","HIIT Vs Snack Exercises on the Academic Stress of University Students: a Randomized Controlled Trial","SHARP-Stress","Inclusion Criteria:\n\n* University students from the 1st to 4th year at the Metropolitan University of Education Sciences and Silva-Henriquez Catholic University\n\nExclusion Criteria:\n\n* High level of physical activity classification in the GPAQ questionnaire.\n* Musculoskeletal conditions that prevent normal physical activity.\n* Cardiac disease that contraindicates high-intensity exercise.\n* Diagnosed mental health condition.","30 Years",{"count":251,"type":20},36,[23],"Mental health among Chilean university students has steadily deteriorated since 2020. One of the factors associated with mental health is the academic workload that comes with transitioning from high school to higher education, which may lead to an increase in stress levels due to university life referred to as academic stress. Academic stress has been linked to multiple negative outcomes in university students, such as a lower quality of life, as well as cardiovascular risk markers, including body composition (e.g., higher fat percentage), muscle function, aerobic capacity, and physical activity levels. Academic stress affecting more than 50% of university students represents a health issue that needs to be addressed, not only because it can lead to chronic stress, but also because it increases cardiovascular risk in a Chilean population where more than 10,000,000 people are overweight, obese, or have insufficient physical activity levels.\n\nAcademic stress and its associated complications represent a prevalent health issue among university students. It is essential to implement interventions that help reduce academic stress while also counteracting its negative effects on quality of life, body composition, muscle function, aerobic capacity, and physical activity levels.\n\nCost-effective tools, both in terms of financial resources and time, are needed. From this perspective, physical exercise meets both requirements, as it is inexpensive to implement and there are various protocols such as high-intensity interval training and \"exercise snacks\" that can require less than 40 minutes per week while providing beneficial effects on academic stress, body composition muscle function, aerobic capacity, and physical activity levels in university students.\n\nExpanding the body of evidence on these different training protocols would allow us to address multiple issues simultaneously. The primary one is academic stress and its related consequences, but also to generate new evidence on aspects not yet covered in the current literature, such as the impact on university students' quality of life, and to provide an accessible treatment tool for the future. Importantly, implementing these short-duration programs would also enable students to maintain their academic responsibilities, as the proposed protocols require no more than 40 minutes per week (\\\u003C10 minutes per day). Finally, these programs could be implemented within university facilities, which, in the long term, could become a permanent tool for improving students' university experience.",[26,27,255,256,257],"Physical Inactivity","Sedentary Behaviors","Cardiovascular Health",[259,260,261,262],"High-intensity Interval Training","Snack Exercises","Academic Stress","Mental Health Well-being","2025-02-25",{"date":265,"type":40},"2025-02-28",{"date":237,"type":20},{"date":268,"type":20},"2025-12-15",{"name":270,"class":47},"Universidad Metropolitana de Ciencias de la Educacion"]