[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"self-compassion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:self-compassion":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,14,0,[8,44,77,110,145,171,203,240,271,300,324,344,370,389],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100592097","compassion-strikes-back-100592097",false,"NCT06988995","Compassion Strikes Back","Compassion Strikes Back: Improving Dyadic Quality of Life for LVAD Patients and Caregivers","Inclusion Criteria:\n\n* LVAD implantation or caregiver or patient with LVAD; over 18 years old; primary caregiver is a family member\n\nExclusion Criteria:\n\n* Currently or in the past 3 months received psychotherapy or psychosocial or peer support; hospitalized for psychiatric reasons in the past 6 months; current, active suicidal thoughts or a reported suicide attempt within the past year; a current alcohol\u002Fsubstance use disorder that required immediate treatment; or a current or past thought disorder, psychosis, or unmanaged bipolar disorder; enrolled in another investigational research\u002Fclinical trial; toxic\u002Fnegative dynamic between pt and caregiver; extended post-LVAD implantation course (i.e., more than 2 months in the hospital).","ALL","18 Years","80 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","Research has shown that LVAD patients and their caregivers typically experience increased mental health concerns and decreased quality of life following LVAD implantation and hospital discharge. The purpose of this study is to explore how to improve quality of life for LVAD patients and their caregivers in the initial transition from hospital to home after LVAD implantation.\n\nOver the course of the study, participants will complete 2 surveys: one when participants are in the hospital and one at a 2-month post-hospital follow-up appointment with the participants' cardiologist. Participants may be contacted if there is data missing from surveys.\n\nParticipants may also be provided with information on improving mental health in the form of handouts or a brief meeting with a psychology provider.",[27,28,29,30],"LVAD Caregivers","LVAD (Left Ventricular Assist Device)","Quality of Life (QOL)","Self-Compassion","RECRUITING","2026-06-25",{"date":34,"type":35},"2026-06-29","ACTUAL",{"date":37,"type":35},"2025-12-01",{"date":39,"type":21},"2026-12",{"name":41,"class":42},"University of Florida","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":51,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":54,"briefSummary":55,"conditions":56,"keywords":62,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":4},"100644161","virtual-reality-for-enhancing-self-compassion-and-reducing-burnout-among-healthcare-providers-100644161","NCT07666867","Virtual Reality for Enhancing Self Compassion and Reducing Burnout Among Healthcare Providers","VR-CF-CBT","Inclusion Criteria:\n\n* have at least one year of experience working in a healthcare setting\n\nExclusion Criteria:\n\n* participating in other behavioral interventions that could confound study results\n* auditory or visual impairments that would interfere with VR usage\n* Participants who experience clinically significant VR-related discomfort\u002Fmotion sickness as assessed by the Simulator Sickness Questionnaire (SSQ)",true,{"count":53,"type":21},52,[24],"Healthcare providers in high-demand clinical settings are at high risk for burnout and secondary traumatic stress due to repeated exposure to patient trauma, which can compromise well-being and quality of care. Compassion-focused cognitive behavioral therapy (CF-CBT) can reduce stress and enhance self-compassion, but traditional delivery is time- and resource-intensive. This project evaluates the feasibility, acceptability, and potential effectiveness of virtual reality (VR)-enhanced CF-CBT specifically adapted for healthcare providers experiencing vicarious trauma. Grounded in Neff's self-compassion framework (emphasizing self-kindness, common humanity, and mindfulness) the VR intervention provides 8 immersive environments where participants can practice compassion-focused skills, engage in procedural learning, and regulate emotional responses in real time.\n\nThe study will be conducted at UC San Diego Health using a two-arm randomized design comparing VR-enhanced CF-CBT with self-guided compassion-focused CBT\u002Fmindfulness exercises delivered without VR. Participants will complete 8 brief VR interventional sessions (approximately 6-10 minutes each) over 4-6 weeks. Outcomes include self-compassion, burnout, and secondary traumatic stress, measured using validated instruments. Feasibility and acceptability will be evaluated through recruitment, retention, session completion, engagement, and participant feedback.\n\nFindings will provide preliminary evidence for VR-enhanced compassion-focused interventions as a scalable and accessible approach to supporting healthcare providers' emotional well-being in demanding clinical environments, and will inform future cultural adaptation and implementation in low-resource and conflict-affected healthcare settings such as those in post-war zones.",[57,58,59,60,61],"Burnout, Healthcare Workers","Burnout","Burnout, Psychological","Self Compassion","Empathy Training of Healthcare Professional Students",[30,63,64,65,66],"Empathy","CBT","Virtual Reality","Healthcare Provider Burnout","NOT_YET_RECRUITING","2026-06-18",{"date":70,"type":35},"2026-06-24",{"date":72,"type":21},"2026-07-01",{"date":74,"type":21},"2027-02-01",{"name":76,"class":42},"University of California, San Diego",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":51,"sex":85,"minAge":17,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":22,"phases":88,"briefSummary":89,"conditions":90,"keywords":94,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":43},"100641373","mindfulness-based-intervention-in-primiparous-pregnant-women-100641373","NCT07660471","Mindfulness-Based Intervention in Primiparous Pregnant Women","Effect of a Mindfulness-Based Intervention on Childbirth Self-Efficacy, Fear of Childbirth, and Self-Compassion in Primiparous Pregnant Women: A Randomized Controlled Trial","MBCP","Inclusion Criteria:\n\n* Pregnant women aged 18 years and older\n* Primiparous women\n* Singleton pregnancy\n* Gestational age between 28 and 32 weeks\n* No known obstetric complications\n* Ability to read and understand Turkish\n* Attendance at the Pregnancy School of the Healthy Life Center\n* Willingness to participate and provide written informed consent\n* Willingness to participate in the mindfulness-based intervention program\n\nExclusion Criteria:\n\n* Multiple pregnancy\n* High-risk obstetric complications (e.g., preeclampsia, gestational diabetes, placenta previa)\n* Diagnosed severe psychiatric disorders (e.g., psychotic disorders, bipolar disorder)\n* Substance or alcohol dependence\n* Previous participation in a structured mindfulness, meditation, or similar awareness-based program\n* Inability to attend intervention sessions regularly","FEMALE",{"count":87,"type":21},128,[24],"This randomized controlled trial aims to evaluate the effect of a mindfulness-based intervention on childbirth self-efficacy, fear of childbirth, and self-compassion among primiparous pregnant women. Eligible pregnant women will be randomly assigned to either a mindfulness intervention group or a control group receiving routine antenatal education and standard prenatal care. The intervention program will consist of eight sessions delivered over four weeks. Outcomes will be assessed before and after the intervention using validated measurement tools. The findings may contribute to the development of effective psychosocial interventions to improve maternal well-being during pregnancy.",[91,92,93,30],"Pregnancy","Fear of Childbirth","Childbirth Self-efficacy",[95,96,91,97,92,98,30,99,100],"Mindfulness","Mindfulness-Based Intervention","Primiparous Pregnant Women","Childbirth Self-Efficacy","Maternal Mental Health","Randomized Controlled Trial","2026-06-16",{"date":103,"type":35},"2026-06-22",{"date":105,"type":21},"2026-06-01",{"date":107,"type":21},"2026-10-31",{"name":109,"class":42},"Agri Ibrahim Cecen University",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":51,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":22,"phases":119,"briefSummary":120,"conditions":121,"keywords":125,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":144},"100642803","a-study-of-a-mental-fitness-intervention-for-anesthesiology-resident-wellbeing-and-self-compassion-100642803","NCT07639827","A Study of a Mental Fitness Intervention for Anesthesiology Resident Wellbeing and Self-Compassion","A Pilot Randomized Controlled Trial of a Mental Fitness Intervention for Anesthesiology Resident Wellbeing and Self-Compassion","Inclusion Criteria:\n\n* Current PGY4 anesthesiology resident at Massachusetts General Hospital or Brigham and Women's Hospital\n* Willingness to provide informed consent\n\nResident Loved One Inclusion Criteria\n\n* The choice of a resident loved one will be at the discretion of the resident.\n* This may include partners, family, friends or other loved ones.\n* Only one individual per resident will be eligible to participate.\n* Residents will be eligible to participate even if no loved one is identified.\n\nExclusion Criteria:\n\n* Inability to complete English-language questionnaires\n* Inability to access and use the intervention components (smartphone app\u002Fweb platform)\n* Age \\\u003C18 years\n* Concurrent participation in another interventional study designed to target mental fitness or wellbeing",{"count":118,"type":21},60,[24],"The goal of this clinical trial is to learn if app-based wellness programs can help improve wellbeing and self-compassion for medical residents. This is a pilot study, which is done on a small group of people to learn if a larger study would be useful. The main questions it aims to answer are:\n\n1. Are app-based wellness interventions feasible and acceptable in a high-stress population like medical residents?\n2. Can app-based wellness programs improve wellbeing and self-compassion in medical residents?\n\nResearchers will compare the app-based wellness program to a time- and attention-matched control program.\n\nParticipants will:\n\n* Complete online questionnaires at the start of the study and again after completion of the wellness program\n* Be assigned by chance (like a coin toss) to one of two different app-based programs, and will participate in the assigned program for 6 weeks. Both programs will involve weekly lessons and brief, daily exercises. Engagement with these exercises will not be mandatory but highly encouraged.",[122,60,58,123,124],"Wellness","Anxiety","Depression",[126,127,128,129,130,131,132,133,134,135],"mental fitness","wellness","self compassion","burnout","app-based intervention","residents","graduate medical education","positive psychology","anxiety","depression","2026-06-13",{"date":101,"type":35},{"date":139,"type":21},"2026-08",{"date":141,"type":21},"2027-01",{"name":143,"class":42},"Massachusetts General Hospital",2,{"id":146,"slug":147,"hasResults":11,"nctId":148,"briefTitle":149,"officialTitle":150,"acronym":151,"eligibilityCriteria":152,"healthyVolunteers":51,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":153,"targetDuration":4,"studyType":22,"phases":155,"briefSummary":156,"conditions":157,"keywords":160,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":166,"completionDateStruct":168,"leadSponsor":170,"locationsCount":4},"100643284","effect-of-mindfulness-based-self-compassion-program-on-self-compassion-secondary-traumatic-stress-and-professional-quality-of-life-in-midwives-and-nurses-working-in-obstetrics-a-randomized-controlled-trial-100643284","NCT07643181","Effect of Mindfulness-Based Self-Compassion Program on Self-Compassion, Secondary Traumatic Stress, and Professional Quality of Life in Midwives and Nurses Working in Obstetrics: A Randomized Controlled Trial","The Effect of Mindfulness-Based Self-Compassion Program on Self-Compassion, Secondary Traumatic Stress, and Professional Quality of Life in Midwives and Nurses Working in Obstetrics: A Randomized Controlled Trial","MBSC-RCT","Inclusion Criteria:\n\n* Working as a midwife or nurse in obstetrics\n* Actively employed in the relevant unit of the study institution\n* 18 years of age or older\n* Able to read and understand Turkish\n* Willing to participate voluntarily in the study\n\nExclusion Criteria:\n\n* Incomplete or incorrect completion of data collection forms\n* Leaving the institution or withdrawing from the study during the research process\n* Failure to complete post-test measurements\n* Having participated in a self-compassion, mindfulness, or similar psychoeducation program within the last six months\n* Intervention group participants are expected to attend at least 80% of program sessions. Participants attending fewer than seven out of eight sessions will be excluded from the analysis.",{"count":154,"type":21},80,[24],"This study aims to examine the effect of a Mindfulness-Based Self-Compassion Program on self-compassion levels, secondary traumatic stress, and professional quality of life in midwives and nurses working in obstetrics. Healthcare professionals in this field are frequently exposed to traumatic experiences such as complicated deliveries, perinatal loss, and obstetric emergencies, which may lead to secondary traumatic stress and reduced professional quality of life over time. This study is designed as a pre-test\u002Fpost-test randomized controlled trial. A total of 80 participants (40 intervention, 40 control) will be recruited from Gaziantep Cengiz Gökçek Obstetrics and Pediatrics Hospital. The intervention group will receive an 8-week Mindfulness-Based Self-Compassion Program (one session per week, 60-90 minutes each). The control group will receive no intervention. Outcomes will be measured before and after the program using validated scales for self-compassion, secondary traumatic stress, and professional quality of life.",[158,30,159],"Secondary Traumatic Stress","Professional Quality of Life",[161,95,162,158,159,30],"Midwives","Nurses","2026-06-08",{"date":165,"type":35},"2026-06-11",{"date":167,"type":21},"2026-07",{"date":169,"type":21},"2026-10",{"name":109,"class":42},{"id":172,"slug":173,"hasResults":11,"nctId":174,"briefTitle":175,"officialTitle":176,"acronym":177,"eligibilityCriteria":178,"healthyVolunteers":51,"sex":16,"minAge":17,"maxAge":179,"enrollmentInfo":180,"targetDuration":4,"studyType":22,"phases":182,"briefSummary":183,"conditions":184,"keywords":187,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":195,"lastUpdatePostDateStruct":196,"startDateStruct":198,"completionDateStruct":200,"leadSponsor":201,"locationsCount":43},"100589867","developing-resilience-in-transgender-and-nonbinary-individuals---exploring-the-impact-of-social-challenges-in-the-metaverse-100589867","NCT06959992","Developing Resilience in Transgender and Nonbinary Individuals - Exploring the Impact of Social Challenges in the Metaverse","Evaluating the Efficacy of Virtual Support Groups Fostering Resilience for Gender Diverse People: a Randomized Clinical Trial in the Metaverse","RESILIDENT","Inclusion Criteria:\n\n* Transgender and nonbinary individuals with a stable gender-identity or questioning\n\nExclusion Criteria:\n\n* Presence of acute psychiatric instability (e.g., acute psychotic symptomatology or acute suicide risk)\n* Not being part of the transgender population\n* Younger than 18","35 Years",{"count":181,"type":21},123,[24],"The goal of this clinical trial is to test the effectiveness of conducting a support group in the Metaverse designed to develop and\u002For improve resilience in gender diverse people. By exploring the impact of different social challenges in a virtual environment, the main question it aims to answer is whether this approach on conducting support group sessions with gender diverse people will strengthen their resilience and associated abilities (self-compassion) compared to a control group and a waitlist.",[185,186,30],"Resilience,Psychological","Well-Being, Psychological",[188,189,190,191,192,193,194],"Metaverse","Gender minorities","Support groups","Resilience","Well-being","Randomized clinical trial","Self-compassion","2026-05-24",{"date":197,"type":35},"2026-05-28",{"date":199,"type":35},"2025-09-01",{"date":39,"type":21},{"name":202,"class":42},"University of Bucharest",{"id":204,"slug":205,"hasResults":11,"nctId":206,"briefTitle":207,"officialTitle":207,"acronym":208,"eligibilityCriteria":209,"healthyVolunteers":51,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":210,"targetDuration":4,"studyType":22,"phases":212,"briefSummary":213,"conditions":214,"keywords":221,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":231,"lastUpdatePostDateStruct":232,"startDateStruct":234,"completionDateStruct":236,"leadSponsor":238,"locationsCount":43},"100634675","choice-and-autonomy-in-learning-mindfulness-for-pediatric-residents-100634675","NCT07542769","Choice and Autonomy in Learning Mindfulness for Pediatric Residents","CALM-PR","Inclusion Criteria:\n\n* Current categorical pediatrics residents at Northwestern University.\n* Preliminary pediatrics residents who intend to continue in pediatrics.\n* Willing and able to provide informed consent.\n\nExclusion Criteria:\n\n\\- None; all pediatric residents meeting inclusion criteria are eligible.",{"count":211,"type":21},42,[24],"This study is a pilot clinical trial designed to evaluate a flexible, online mindfulness program for pediatric residents. Medical training can be stressful, and although mindfulness programs are often offered to support well-being, many are either in-person or follow a fixed format that may not fit individual schedules or preferences. This study will test a digital mindfulness program called Wakeful, which allows participants to complete the course at their own pace. Participants will be randomly assigned to one of two groups: one group will be able to choose the length of their mindfulness program (3, 5, or 7 weeks), while the other group will be assigned a program length without a choice. The goal is to understand whether giving participants a choice improves how often they use the program, how satisfied they are with it, and whether they complete it. The main outcomes of this study focus on how participants interact with the program, including how many sessions they complete, how often they practice mindfulness on their own, and how useful and relevant they find the program. The study will also look at overall satisfaction and how many participants drop out before finishing. In addition, the study will explore whether participants report changes in mindfulness and compassion for others, although it is not designed to determine clinical improvements in mental health. By understanding how pediatric residents engage with different program formats, this study aims to inform the design of more flexible and user-centered digital wellness programs that better fit into demanding medical training environments.",[215,216,95,30,217,218,219,220],"Program Engagement","Treatment Adherence and Compliance","Physician Burnout","Psychological Well-Being","Meditation","Meditation Training",[95,219,222,223,224,225,226,216,227,215,228,229,30,230],"Digital Health Intervention","Internet-Based Intervention","Physician Well-Being","Graduate Medical Education","Pediatric Residency","Patient Acceptance of Health Care","User Engagement","Pilot Projects","Compassion","2026-05-21",{"date":233,"type":35},"2026-05-26",{"date":235,"type":35},"2026-04-13",{"date":237,"type":21},"2027-05-01",{"name":239,"class":42},"Northwestern University",{"id":241,"slug":242,"hasResults":11,"nctId":243,"briefTitle":244,"officialTitle":245,"acronym":4,"eligibilityCriteria":246,"healthyVolunteers":51,"sex":16,"minAge":247,"maxAge":4,"enrollmentInfo":248,"targetDuration":4,"studyType":250,"phases":4,"briefSummary":251,"conditions":252,"keywords":257,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":262,"lastUpdatePostDateStruct":263,"startDateStruct":265,"completionDateStruct":267,"leadSponsor":269,"locationsCount":43},"100621397","self-compassion-self-efficacy-and-health-outcomes-in-older-adults-100621397","NCT07370090","Self-Compassion, Self-Efficacy, and Health Outcomes in Older Adults","The Effect of Self-Compassion and Self-Efficacy on Postural Awareness, Pain, and Health-Promoting Lifestyle Behaviors in Older Adults","Inclusion Criteria:\n\n* Aged 65 years and older\n* Able to read and understand Turkish\n* Able to complete online questionnaires independently\n* Provided informed consent\n\nExclusion Criteria:\n\n* Diagnosis of severe cognitive impairment (e.g., dementia or Alzheimer's disease)\n* Severe psychiatric disorders (e.g., schizophrenia or bipolar disorder)\n* Inability to complete questionnaires independently\n* Incomplete or inconsistent questionnaire responses","65 Years",{"count":249,"type":21},150,"OBSERVATIONAL","This cross-sectional observational study aims to examine the relationship between self-compassion, self-efficacy, postural awareness, pain, quality of life, and health-promoting lifestyle behaviors in adults aged 65 years and older. Data will be collected using validated self-report questionnaires administered online. The findings are expected to contribute to a better understanding of psychological factors associated with physical and behavioral health outcomes in older adults.",[253,254,30,255,256],"Older Adults (65 Years and Older)","Health Behavior","Self-Efficacy","Pain",[194,258,259,260,261,256],"Self-efficacy","Older adults","Postural awareness","Health-promoting lifestyle","2026-01-19",{"date":264,"type":35},"2026-01-27",{"date":266,"type":21},"2026-01-15",{"date":268,"type":21},"2026-03-01",{"name":270,"class":42},"Acibadem University",{"id":272,"slug":273,"hasResults":11,"nctId":274,"briefTitle":275,"officialTitle":276,"acronym":277,"eligibilityCriteria":278,"healthyVolunteers":11,"sex":16,"minAge":279,"maxAge":4,"enrollmentInfo":280,"targetDuration":4,"studyType":22,"phases":282,"briefSummary":283,"conditions":284,"keywords":289,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":291,"lastUpdatePostDateStruct":292,"startDateStruct":294,"completionDateStruct":296,"leadSponsor":298,"locationsCount":43},"100598069","mindfulness-and-compassion-program-for-the-improvement-of-emotional-and-behavioral-problems-academic-performance-and-school-climate-in-students-in-the-last-cycle-of-primary-education-100598069","NCT07066696","Mindfulness and Compassion Program for the Improvement of Emotional and Behavioral Problems, Academic Performance and School Climate in Students in the Last Cycle of Primary Education.","Mindfulness and Compassion Program for the Improvement of Emotional and Behavioral Problems, Academic Performance and School Climate in Students in the Last Cycle of Primary Education (Cuida2 Project)","Cuida2","Inclusion Criteria:\n\n* To be a pupil, parent\u002Fguardian of a child or minor under guardianship or academic tutor in the 5th or 6th year of Primary Education.\n* Fluent in Spanish.\n* Provided informed consent.\n\nExclusion Criteria:\n\n* Participant's decision to withdraw from the study at any point","10 Years",{"count":281,"type":21},448,[24],"This randomized controlled trial aims to evaluate the efficacy of a Mindfulness and Compassion program to improve emotional and behavioral problems, academic performance and school climate of students in the last cycle of Primary Education.\n\nParticipants will be randomly assigned to the Cuida2 program or to an active control group practicing relaxation.\n\nThe different variables studied will be evaluated before and after the intervention, and at a three months follow-up. These evaluations will be carried out by the students and their families. In addition, a qualitative exploration will be carried out at the end of the programs, also including the teachers' perceptions.",[95,230,30,285,286,287,288],"Academic Performance","School Climate","Mental Health","Primary School Students",[95,230,194,288,290,286,285],"Emotional and Behavioural Problems","2025-07-04",{"date":293,"type":35},"2025-07-15",{"date":295,"type":21},"2025-10-06",{"date":297,"type":21},"2027-01-30",{"name":299,"class":42},"Universidad de Zaragoza",{"id":301,"slug":302,"hasResults":11,"nctId":303,"briefTitle":304,"officialTitle":305,"acronym":306,"eligibilityCriteria":307,"healthyVolunteers":51,"sex":85,"minAge":17,"maxAge":179,"enrollmentInfo":308,"targetDuration":4,"studyType":22,"phases":309,"briefSummary":310,"conditions":311,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":315,"lastUpdatePostDateStruct":316,"startDateStruct":318,"completionDateStruct":320,"leadSponsor":322,"locationsCount":43},"100589919","nature-for-body-image-100589919","NCT06960668","Nature for Body Image","Look at the Bright (Nature) Side: Improving Body Image and Associated Protective Factors and Reducing Body Image Threats With the Nature for Body Image (NBI) Project","NBI","Inclusion Criteria:\n\n* Females\n* Age 18-35 years old\n\nExclusion Criteria:\n\n* Full-blown body image disorder",{"count":118,"type":21},[24],"Nature exposure has been found to be particularly beneficial for body image, as recent studies have identified a positive association between time spent in nature and positive body image. Positive body image, defined as the ability to accept and respect one's body, has been linked to greater life satisfaction and engagement in healthy behaviors. Conversely, negative body image is recognized as a public health concern due to its detrimental effects on both physical and mental health. It has been associated with symptoms of Body Image Disorders (BIDs), including Eating Disorders (EDs) and Body Dysmorphic Disorder (BDD).\n\nThe Nature for Body Image (NBI) project aimed to examine the impact of a structured nature exposure intervention on improving body image among young women aged 18-35 years.",[312,313,30,314],"Body Image","Eating Behaviors","Interoception","2025-05-15",{"date":317,"type":35},"2025-05-16",{"date":319,"type":35},"2025-05-01",{"date":321,"type":21},"2026-02-28",{"name":323,"class":42},"University of Padova",{"id":325,"slug":326,"hasResults":11,"nctId":327,"briefTitle":328,"officialTitle":328,"acronym":4,"eligibilityCriteria":329,"healthyVolunteers":51,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":330,"targetDuration":4,"studyType":22,"phases":332,"briefSummary":333,"conditions":334,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":335,"lastUpdatePostDateStruct":336,"startDateStruct":338,"completionDateStruct":340,"leadSponsor":342,"locationsCount":43},"100557475","online-mindful-self-compassion-training-for-medical-students-an-exploratory-feasibility-study-100557475","NCT06538597","Online Mindful Self-Compassion Training for Medical Students: an Exploratory Feasibility Study","Inclusion Criteria:\n\n1. Enrolled in first or second-year of the MD or MD\u002FPhD program at the University of Toronto,\n2. Over 18 years of age,\n3. Able to speak, read, and write in English,\n4. Willing to take part in the SCHC course for up to the full 6-week duration,\n5. Willing to complete all study related questionnaires\n\nExclusion Criteria:\n\n1\\. Those already having completed a mindful self-compassion course or Mindfulness based-intervention (Mindfulness-based stress reduction or Mindfulness-based cognitive therapy) within the past 12 months.",{"count":331,"type":21},45,[24],"The goal of this clinical trial is to develop and investigate a compassion-based intervention (Self-Compassion for Healthcare Communities (SCHC) course) in medical students. The main objectives are:\n\n1. Explore the feasibility of trial processes including recruitment, adherence, retention, and follow-up\n2. Explore the experiences of medical students with the Compassion-based intervention, including perceived effects, barriers and facilitators to participation, suggestions for improvement\n3. Determine potential effects on burnout, compassion fatigue, compassion satisfaction, self-compassion, compassion for others, empathy, mindfulness, perceived stress, and emotional regulation.\n\nParticipants will be asked to take part in a 6-week online Self-Compassion for Healthcare Communities course and report changes in levels of burnout, compassion fatigue, compassion satisfaction, self-compassion, compassion for others, empathy, mindfulness, perceived stress, and emotional regulation from pre- to post-intervention and at 3-month follow-up. Additionally, participants will be asked to take part in a semi-structured interview to explore their experiences with the course, perceived effects, and suggestions for improvement.",[30],"2025-03-25",{"date":337,"type":35},"2025-03-30",{"date":339,"type":35},"2025-02-01",{"date":341,"type":21},"2025-08",{"name":343,"class":42},"Robert Simpson",{"id":345,"slug":346,"hasResults":11,"nctId":347,"briefTitle":348,"officialTitle":349,"acronym":4,"eligibilityCriteria":350,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":351,"targetDuration":4,"studyType":22,"phases":353,"briefSummary":354,"conditions":355,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":361,"lastUpdatePostDateStruct":362,"startDateStruct":364,"completionDateStruct":366,"leadSponsor":368,"locationsCount":43},"100578607","eastern-principles-acceptance-and-commitment-therapy-for-injury-prevention-among-nurses-and-nursing-aides-100578607","NCT06813495","Eastern Principles Acceptance and Commitment Therapy For Injury Prevention Among Nurses and Nursing Aides","Prevention of Injuries Among Nurses and Nursing Aides Using Eastern Principles Acceptance and Commitment Therapy: Clinical Trial and Dissemination Research","Inclusion Criteria:\n\n* USA: Employed as a nurse or nursing aide in a long-term care facility within a 120 mile radius of Bowling Green, Ohio.\n* Thailand: Employed as a nurse or nursing aide in Chiang Mai, Thailand or Krung Thep Bangkok), Thailand.\n* At least 18 years of age.\n* Able to attend scheduled assessment and intervention appointments.\n\nExclusion Criteria:\n\n• There are no a-priori exclusion criteria. However, if a participant reports significant psychological distress or a diagnosable mental health condition at the baseline assessment, they will be referred for an alternative treatment.",{"count":352,"type":21},255,[24],"This clinical trial will evaluate the effectivness of an Eastern Principles Acceptance and Commitment Therapy intervention (EPACT) relative to an estabished traditional Western-based Acceptance and Commitment Therapy intervention (ACT) and a no treatment control group. The participants for the study will be nurses and nursing aides (NNAs) who work in long-term care settings in the USA and Thailand. The primary dependent variables are work-related injuries, work stress and burnout, wellbeing, musculoskeletal symptoms, time off from work due to injury. High frequency heart rate variability will also be investigated as a predictor of responsiveness to the interventions.\n\nThe study has three primary aims:\n\n1. To compare the EPACT NNA intervention to an established traditional Western ACT NNA intervention and a no-treatment control group.\n2. To identify predictors of ACT NNA and EPACT NNA responsiveness to the interventions and injury likelihood across time.\n3. To assess EPACT NNA's feasibility and effectiveness across cultures.\n\nUSA participants working in Ohio will be randomly assigned to one of three groups: EPACT NNA (n = 80), ACT NNA (n = 80), or a no treatment control group (n = 80). All participants will participate in an assessment session where study questnnaires are completed and a baseline high frequency HRV measurement is collected. Subsequent to the assessment, the EPACT NNA and ACT NNA participants will attend two 2.5 hour sessions spaced one week apart. The control group will have no further in-person meetings with the researchers. One-month after completing the intervention (4 weeks after the baseline assessment) a follow-up survey will be sent to participants for the first follow-up. Three months after baseline, the second follow-up survey will be sent to participants.\n\nThe surveys assess demographic characteristics, organizational variables, work-related injuries, work stress, and well-being.\n\nA second RCT study will be conducted in Thailand comparing EPACT NNA (n = 40) to a no-treatment control group (n = 40) among nurses and nursing aides working in healthcare settings. The same outcome measures and procedures will be used.\n\nThis research aims to develop a culturally-informed, evidence-based intervention that integrates both Western and Eastern mindfulness principles to address the high rates of work-related injuries among NNAs.",[186,356,357,358,58,95,30,359,360],"Work Injury","Musculoskeletal Pain","High Frequency Heart Rate Variability","Acceptance and Commitment Therapy","Heart Rate Variability","2025-02-03",{"date":363,"type":35},"2025-02-07",{"date":365,"type":35},"2023-05-01",{"date":367,"type":21},"2026-05-01",{"name":369,"class":42},"Bowling Green State University",{"id":371,"slug":372,"hasResults":11,"nctId":373,"briefTitle":374,"officialTitle":374,"acronym":4,"eligibilityCriteria":375,"healthyVolunteers":51,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":376,"targetDuration":4,"studyType":250,"phases":4,"briefSummary":378,"conditions":379,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":381,"lastUpdatePostDateStruct":382,"startDateStruct":384,"completionDateStruct":386,"leadSponsor":387,"locationsCount":43},"100563818","focus-group-study-on-the-feeling-tone-mindfulness-course-100563818","NCT06621108","Focus Group Study on the Feeling Tone Mindfulness Course","Inclusion Criteria:\n\n* Aged 18 or above\n* Speak and understand Cantonese as well as written Chinese to a level where the participant can fully take part in the focus group session without the need for translation support\n* Have means to access online teleconferencing meeting software (e.g., Zoom), online surveys (to give their informed consent and to schedule a focus group session), online materials, and Short Message Service (SMS) or WhatsApp messenger.\n* Participants who have completed the four-week feeling tone mindfulness course\n\nExclusion Criteria:\n\n* N\u002FA",{"count":377,"type":21},25,"This is an academic research study aiming to explore the acceptability, feasibility, and effectiveness of a four-week feeling tone mindfulness course by gathering qualitative feedback from course participants in a focus group format.",[95,30,124,123,380,192],"Stress","2024-09-29",{"date":383,"type":35},"2024-10-01",{"date":385,"type":21},"2024-10",{"date":39,"type":21},{"name":388,"class":42},"The University of Hong Kong",{"id":390,"slug":391,"hasResults":11,"nctId":392,"briefTitle":393,"officialTitle":393,"acronym":4,"eligibilityCriteria":394,"healthyVolunteers":51,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":395,"targetDuration":4,"studyType":22,"phases":396,"briefSummary":397,"conditions":398,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":400,"lastUpdatePostDateStruct":401,"startDateStruct":403,"completionDateStruct":404,"leadSponsor":405,"locationsCount":43},"100561875","acceptability-feasibility-and-effectiveness-of-a-four-week-feeling-tone-mindfulness-course-100561875","NCT06595849","Acceptability, Feasibility, and Effectiveness of a Four-Week Feeling Tone Mindfulness Course","Inclusion Criteria:\n\n* aged 18 or above\n* speak and understand Cantonese as well as written Chinese to a level where the participant can fully take part in the course without the need for translation support\n* have means to access online teleconferencing meeting software (e.g., Zoom), online surveys, online intervention materials, and Short Message Service (SMS) or WhatsApp messenger\n\nExclusion Criteria:\n\n* moderately severe or severe depressive or anxiety symptoms\n* diagnosed with bipolar disorder or bipolar affective disorder (type I or type II) or ever experienced a manic\u002Fhypomanic episode\n* diagnosed with schizophrenia\u002F psychosis or ever experienced a psychotic episode\n* diagnosed with dementia\u002F neurocognitive disorders\u002F neurological disorders\n* diagnosed with intellectual disability\n* diagnosed with other neurodevelopmental disorders\n* experience of a traumatic event that is currently affecting the potential participants\n* recent bereavement, major loss, or stressful life events\n* suicidal\n* alcohol or drug abuse\n* currently experiencing other mental or physical health condition, or life condition that might affect potential participants' participation in the course\n* prior experience of taking part in the feeling tone intervention as a course participant",{"count":154,"type":21},[24],"This is an academic research study aiming to explore the acceptability, feasibility, and effectiveness of a four-week feeling tone mindfulness course on equanimity, mindfulness, self-compassion, and mental health outcomes.",[95,124,123,380,399,194],"Wellbeing","2024-09-11",{"date":402,"type":35},"2024-09-19",{"date":385,"type":21},{"date":139,"type":21},{"name":388,"class":42}]