[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"emotional-well-being\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:emotional-well-being":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,49,83,111,135],{"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":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":4},"100640136","robotic-dog-intervention-on-emotional-well-being-and-quality-of-life-100640136",false,"NCT07607379","Robotic Dog Intervention on Emotional Well-Being and Quality of Life","Effectiveness and Feasibility of a Robotic Dog Intervention on Emotional Well-Being and Quality of Life in Pediatric Patients With Hematological Malignancies Undergoing HSCT","ROBDOG","Inclusion Criteria:\n\n* Pediatric patients aged 8-15 years\n* Diagnosed with a hematological malignancy and undergoing hematopoietic stem cell transplantation\n* Hospitalized in a protective isolation room during the post-transplant inpatient period\n* Expected to remain hospitalized under isolation for approximately 30 days post-transplant\n* Able to understand and respond to Turkish-language self-report questionnaires\n* Clinically stable and deemed eligible for participation by the treating clinical team\n* Able to interact with the robotic dog at a basic functional level\n\nExclusion Criteria:\n\n* Severe cognitive impairment or neurodevelopmental conditions preventing meaningful interaction or self-report\n* Acute neurological conditions, delirium, or severe psychiatric crisis (e.g., acute agitation, suicidal ideation)\n* Requirement for intensive care, invasive ventilation, or a clinically unstable condition\n* Severe visual, hearing, or motor impairments that prevent interaction with the robotic dog\n* Additional infection control restrictions prevent the placement or use of the robotic dog in the isolation room\n* Anticipated early discharge, transfer, or inability to complete follow-up assessments\n* Severe fear, intolerance, or refusal to interact with robotic or electronic devices","ALL","8 Years","15 Years",{"count":21,"type":22},28,"ESTIMATED","INTERVENTIONAL",[25],"NA","The hematopoietic stem cell transplantation (HSCT) process imposes a substantial psychological burden, leading to impaired emotional well-being due to intensive treatment, isolation, and immunosuppression. Patients often experience social withdrawal, loneliness, and loss of control, which may result in persistent anxiety, depressive symptoms, and reduced quality of life (QoL) if unaddressed. This study aims to evaluate the effectiveness, feasibility, and acceptability of an AI-powered robotic dog in improving emotional well-being and QoL in pediatric patients undergoing HSCT.",[28,29,30],"Emotional Well-being","Quality of Life","Pediatric Oncology",[32,33,34,35,36],"technology","pediatric oncohematology","Hematological Malignancy","well-being","nurse","NOT_YET_RECRUITING","2026-05-19",{"date":40,"type":41},"2026-05-26","ACTUAL",{"date":43,"type":22},"2026-07-01",{"date":45,"type":22},"2028-06-30",{"name":47,"class":48},"Koç University","OTHER",{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":17,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":23,"phases":61,"briefSummary":62,"conditions":63,"keywords":66,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":82},"100635322","mandala-activity-for-anxiety-and-emotional-and-psychological-well-being-in-adolescents-with-siblings-with-special-needs-100635322","NCT07551180","Mandala Activity for Anxiety and Emotional and Psychological Well-Being in Adolescents With Siblings With Special Needs","Effect of a Mandala Activity on Anxiety Levels and Emotional and Psychological Well-Being in Adolescents Who Have Siblings With Special Needs: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adolescents within the predefined study age range\n* Having a sibling with special needs\n* Ability to communicate in Turkish\n* Willingness to participate in the study\n* Written informed consent from a parent or legal guardian and assent from the adolescent\n* Availability to attend the planned intervention and assessment sessions\n\nExclusion Criteria:\n\n* Having any physical, cognitive, or communication problem that would prevent participation in the mandala activity program or completion of the measurement tools\n* Not attending the planned intervention sessions\n* Withdrawal of consent\u002Fassent during the study period",true,"10 Years","19 Years",{"count":60,"type":22},64,[25],"The purpose of this randomized controlled trial is to evaluate whether a structured mandala activity program can reduce anxiety and improve emotional and psychological well-being in adolescents who have a sibling with special needs. Adolescents in this group may experience emotional difficulties because of the demands and challenges associated with having a sibling who requires special care and support. However, supportive and accessible interventions for these adolescents are limited.\n\nIn this study, eligible participants will be randomly assigned to either an intervention group or a control group. The intervention group will participate in a structured mandala activity program, while the control group will not receive this program during the study period. Anxiety and emotional and psychological well-being will be assessed before and after the intervention using standardized measurement tools.\n\nThe main question of this study is whether participation in the mandala activity program leads to better mental well-being outcomes compared with the control group. The findings may help determine whether mandala-based activities can be used as a simple, supportive, and non-pharmacological approach for adolescents who have a sibling with special needs.",[64,28,65],"Anxiety","Psychological Well-being",[67,68,69,70,71,64,72],"Adolescents","Siblings with Special Needs","Mandala Activity","Emotional Well-Being","Psychological Well-Being","Randomized Controlled Trial","2026-04-20",{"date":75,"type":41},"2026-04-24",{"date":77,"type":22},"2026-05-02",{"date":79,"type":22},"2026-06-30",{"name":81,"class":48},"Akdeniz University",1,{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":89,"eligibilityCriteria":90,"healthyVolunteers":56,"sex":17,"minAge":91,"maxAge":92,"enrollmentInfo":93,"targetDuration":4,"studyType":23,"phases":95,"briefSummary":96,"conditions":97,"keywords":100,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":4},"100618419","eft-and-resilience-in-nursing-students-100618419","NCT07331376","EFT and Resilience in Nursing Students","Improving Perceived Stress, Anxiety, and Sleep Quality Among Nursing Students: Enhancing Resilience Through Emotional Freedom Techniques","Emotional","Inclusion Criteria:\n\n* Currently enrolled in the Nursing Department at Muş Alparslan University,\n* Be 18 years of age or older,\n* Agree to participate in the study voluntarily,\n* Have no psychiatric diagnosis or regular use of psychotropic medication.\n\nExclusion Criteria:\n\nStudents who do not regularly participate in the application process,\n\n* Students who do not complete the data collection forms in full,\n* Students who report physical or psychological discomfort during the EFT application process.","18 Years","24 Years",{"count":94,"type":22},105,[25],"The purpose of this study is to determine the effect of Emotional Freedom Technique (EFT) application on stress, anxiety, and sleep quality in nursing students.\n\nThe nursing education process can cause high levels of psychological and physiological stress in students due to many factors such as a heavy theoretical knowledge load, clinical practice stress, exam anxiety, and shift work. This situation results in increased anxiety and impaired sleep quality, thereby negatively affecting students' academic performance, clinical skills, and overall well-being.\n\nIn this context, the study aims to evaluate whether EFT, as a complementary method, is effective in reducing stress and anxiety levels in nursing students, as well as improving sleep quality.\n\nIt is believed that the results of this research will contribute to the development of alternative approaches that support psychological well-being in nursing education and will provide evidence-based data on the integration of EFT into educational programs.",[28,98,99],"Sleep Quality","Nursing Students",[99,98,101],"Emotional Freedom Techniques (EFT)","2025-12-30",{"date":104,"type":41},"2026-01-09",{"date":106,"type":22},"2025-12-22",{"date":108,"type":22},"2026-06-20",{"name":110,"class":48},"Hasan Kalyoncu University",{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":56,"sex":17,"minAge":91,"maxAge":118,"enrollmentInfo":119,"targetDuration":4,"studyType":23,"phases":121,"briefSummary":122,"conditions":123,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":4},"100588553","evaluation-of-a-dietary-supplement-containing-melissa-officinalis-formulated-in-phospholipids-on-mood-well-being-and-cortisol-modulation-100588553","NCT06942897","Evaluation of a Dietary Supplement Containing Melissa Officinalis Formulated in Phospholipids on Mood Well-being and Cortisol Modulation","Pilot Study for the Evaluation of a Dietary Supplement Containing Melissa Officinalis Formulated in Phospholipids on Mood Well-being and Cortisol Modulation","Inclusion Criteria:\n\n* Age between 18 and 65 years\n* Healthy volunteers as assessed by medical history and physical examination\n* Willingness to comply with the study procedures\n\nExclusion Criteria:\n\n* Current use of medications or supplements that may affect mood or cortisol levels\n* Known allergy or sensitivity to Melissa officinalis or phospholipids\n* History of psychiatric disorders (e.g., major depression, anxiety disorders)\n* Significant comorbidities (e.g., cardiovascular, hepatic, renal diseases)\n* Pregnant or breastfeeding women\n* Participation in another clinical trial in the past 30 days","65 Years",{"count":120,"type":22},40,[25],"This is a randomized, double-blind, placebo-controlled pilot study designed to evaluate the effect of an oral nutritional supplement containing Melissa officinalis formulated in phospholipids on mood and cortisol levels in healthy adults. Participants will be randomly assigned to receive either the active supplement or a placebo daily for 3 weeks. The primary outcome measures include changes in mood well-being, perceived stress, and salivary cortisol levels. The study aims to assess both efficacy and safety of the supplement in modulating stress response and emotional balance.",[124,125,28],"Stress","Mood Disorders","2025-11-23",{"date":128,"type":41},"2025-11-25",{"date":130,"type":22},"2026-06-15",{"date":132,"type":22},"2026-09-15",{"name":134,"class":48},"Azienda di Servizi alla Persona di Pavia",{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":4,"eligibilityCriteria":141,"healthyVolunteers":56,"sex":17,"minAge":118,"maxAge":4,"enrollmentInfo":142,"targetDuration":4,"studyType":23,"phases":144,"briefSummary":145,"conditions":146,"keywords":149,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":153,"lastUpdatePostDateStruct":154,"startDateStruct":156,"completionDateStruct":158,"leadSponsor":160,"locationsCount":4},"100574782","art-therapy-for-enhancing-well-being-in-solitary-older-adults-100574782","NCT06763757","Art Therapy for Enhancing Well-Being in Solitary Older Adults","Art Application and Transformation on Solitary Seniors.","Inclusion Criteria:\n\n1. Age 65 years or older.\n2. Living alone.\n3. Mini-Mental State Examination (MMSE) score between 24 and 30, indicating no significant cognitive impairment.\n4. Capable of providing informed consent.\n5. Physically able to participate in art-related activities such as drawing or painting.\n6. Not currently undergoing psychiatric medication treatment for conditions such as depression, anxiety, schizophrenia, or bipolar disorder.\n\nExclusion Criteria:\n\n1. Recent major life events (e.g., bereavement, severe illness) that could interfere with study participation.\n2. History of brain injury or severe psychiatric conditions, such as schizophrenia or major depressive disorder requiring hospitalization.\n3. Physical disabilities or motor impairments that prevent participation in art activities.\n4. Participation in similar art therapy studies within the past 6 months.\n5. Strong aversion or resistance to art therapy activities.",{"count":143,"type":22},22,[25],"This study explores the impact of art therapy on mental health and quality of life among solitary older adults. Participants will be randomly assigned to one of two groups: an experimental group receiving art therapy sessions or a control group with no intervention. The art therapy program includes 12 weekly sessions lasting 90 minutes each, focusing on creative expression, observation of art, and reflective discussions. These activities are designed to enhance emotional well-being, reduce depressive symptoms, and foster interpersonal connections.\n\nBoth groups will undergo evaluations before and after the 12-week study period. The assessments will include the Taiwanese version of the WHO Quality of Life-BREF (WHOQOL-BREF) and the Beck Depression Inventory (BDI) to measure changes in psychological health and life satisfaction. The findings aim to demonstrate the feasibility and benefits of art therapy as a non-pharmacological intervention for improving the well-being of solitary older adults.",[147,29,28,148],"Mental Health","Loneliness",[150,151,147,29,152],"Occupational Therapy","Solitary Older Adults","Art Therapy","2025-01-08",{"date":155,"type":41},"2025-01-10",{"date":157,"type":22},"2025-01-07",{"date":159,"type":22},"2025-05-31",{"name":161,"class":48},"National Taiwan University Hospital"]