[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"children-with-cancer\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:children-with-cancer":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,70,93],{"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":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100540719","evaluation-of-the-effect-of-a-physical-activity-recovery-stay-100540719",false,"NCT06320496","Evaluation of the Effect of a Physical Activity Recovery Stay","Evaluation of the Effect of a Physical Activity Recovery Stay on the Physical Condition and Quality of Life of Children in a Situation of Physical Deconditioning","Inclusion Criteria:\n\n* Children with a pathology (chronic disease, rare disease or disability) in a state of deconditioning to exercise\n* Taken in charge at the CMPRE for a stay to resume physical activity\n\nExclusion Criteria:\n\n* Age under 8 and over 18\n* Patients undergoing rehabilitation during the stay\n* Patients with a significant change in their therapeutic management during the stay\n* Significant cognitive impairment preventing comprehension of instructions\n* Significant club or leisure sports activity (3x\u002Fweek)\n* Electric wheelchair\n* Non-compliance with stay (5 ½ days missed out of total stay)\n* Participation in another study during the return-to-physical-activity stay","ALL","8 Years","18 Years",{"count":20,"type":21},50,"ESTIMATED","OBSERVATIONAL","A WHO study in 2020 revealed that 81% of adolescents (aged 11-17) do not respect the recommendation of one hour of moderate physical activity per day. In the context of disability, many factors impose limits on physical activity. While the pathology itself induces limitations and restrictions (prolonged sitting time, assisted movement, etc.), organizational constraints also apply to both children and parents, who have to divide their time between work, school and therapeutic care, which is sometimes numerous and varied over the course of a single week. These limitations generate stress and fatigue, and prolonged sedentary periods lead children with chronic illnesses, rare diseases or disabilities into a process of physical deconditioning. The accumulation of sedentary time is detrimental to cardiovascular and metabolic health.\n\nTo combat this deconditioning, the 2008 National Physical Activity and Sport Plan (PNAPS) sets out the main guidelines for treatment and implementation. The plan explains that \"for patients with chronic illnesses, rare diseases or disabilities, the aim is to encourage care and guidance towards Adapted Physical Activity (APA). The attending physician will be able to identify local therapeutic education programs, rehabilitation services and \"sport-santé\" offers, to improve access for these patients to supervised local programs\". In addition, the plan suggests \"developing APA programs in healthcare establishments to enable people with chronic illnesses, rare diseases or disabilities to access health education incorporating practical sessions\".\n\nIn line with this plan, an exercise reconditioning program has been set up at our facility. This three-month stay includes children with a variety of pathologies, but with a common feature of physical deconditioning.",[25,26],"Children With Cerebral Palsy","Children With Cancer","RECRUITING","2026-05-04",{"date":30,"type":31},"2026-05-08","ACTUAL",{"date":33,"type":31},"2022-03-22",{"date":35,"type":21},"2026-09",{"name":37,"class":38},"Union de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":18,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":55,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":4},"100621163","four-life-domains-vision-board-program-100621163","NCT07367048","Four Life Domains Vision Board Program","The Effect of the Four Life Domains Vision Board Program on Hope and Psychological Resilience in Adolescents Undergoing Cancer Treatment: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adolescents aged 12-18\n* Has been receiving cancer treatment for at least 6 months\n* Able to communicate in Turkish\n* Not in the terminal stage\n\nExclusion Criteria:\n\n* Those who have experienced a serious traumatic life event in the last 6 months\n* Those with a psychiatric diagnosis\n* Those with a medical condition that would prevent participation in the intervention","12 Years",{"count":49,"type":21},60,"INTERVENTIONAL",[52],"NA","This randomized controlled trial aims to evaluate the effect of a Four Life Domains-Based Vision Board Program on hope and psychological resilience among adolescents undergoing cancer treatment. Adolescents receiving cancer treatment often experience psychological distress that may negatively affect their sense of hope and resilience. Vision board-based psychosocial interventions grounded in positive psychology and creative expression may support adaptive coping and emotional well-being.\n\nThe study will be conducted in pediatric hematology-oncology units of Gazi University Health Application and Research Center and Etlik City Hospital in Türkiye. A total of 60 adolescents aged 12-18 years who have been receiving cancer treatment for at least six months will be randomly assigned to either the intervention group (n=30) or the control group (n=30).\n\nParticipants in the intervention group will receive a structured 5-week Four Life Domains-Based Vision Board Program, consisting of four core modules and one reinforcement session, while the control group will receive standard hospital care only. Outcome measures, including hope and psychological resilience, will be assessed at baseline and after completion of the intervention. The findings are expected to contribute to the development of innovative and holistic psychosocial support interventions for adolescents undergoing cancer treatment.",[26],[56,57,58,59],"adolescent cancer","Vision board intervention","hope","Psychosocial intervention","NOT_YET_RECRUITING","2026-01-17",{"date":63,"type":31},"2026-01-26",{"date":65,"type":21},"2026-01-30",{"date":67,"type":21},"2027-03-20",{"name":69,"class":38},"Gazi University",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":77,"maxAge":18,"enrollmentInfo":78,"targetDuration":4,"studyType":50,"phases":79,"briefSummary":80,"conditions":81,"keywords":82,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":89,"startDateStruct":90,"completionDateStruct":91,"leadSponsor":92,"locationsCount":4},"100621162","art-based-emotion-regulation-program-100621162","NCT07367035","Art-Based Emotion Regulation Program","The Effect of an Art-Based Emotion Regulation Program on Anxiety, Emotion Regulation Skills, and Symptom Burden in Adolescents Undergoing Cancer Treatment: A Randomized Controlled Trial","* Inclusion Criteria for the Study:\n\n  1. Receiving cancer treatment for at least 6 months,\n  2. Aged between 10 and 18 years,\n  3. The participant and their parent\u002Fguardian consent to participate in the study and provide written informed consent.\n\nExclusion Criteria:\n\n1. Those who have experienced a significant life event (death, relocation, etc.) unrelated to their illness in the last six months,\n2. Those who have not received chemotherapy treatment,\n3. Those in the terminal stage,\n4. Those with a severe psychological diagnosis and taking medication","10 Years",{"count":49,"type":21},[52],"Adolescents receiving cancer treatment often experience increased anxiety, difficulties in emotion regulation, and a high symptom burden due to treatment-related physical effects and psychosocial stressors. Supportive, non-pharmacological interventions that promote emotional regulation are therefore needed.\n\nThe purpose of this randomized controlled trial is to evaluate the effect of an art-based emotion regulation program on anxiety levels, emotion regulation skills, and symptom burden in adolescents undergoing cancer treatment.\n\nThis single-blind, parallel-group randomized controlled study will include 60 adolescents aged 10-18 years receiving cancer treatment at Gazi University Health Application and Research Center and Etlik City Hospital Pediatric Hematology-Oncology units between January 30, 2026 and March 20, 2027. Participants will be randomly assigned to either the intervention group or the control group. The intervention group will receive a 4-week art-based emotion regulation program, while the control group will receive routine care. Outcomes will be assessed using validated self-report measures at baseline and at the end of the intervention period.",[26],[83,84,85,86,87,88],"Adolescent Cancer","Pediatric Oncology","Art-Based Intervention","Emotion Regulation","Anxiety","Symptom Burden",{"date":63,"type":31},{"date":65,"type":21},{"date":67,"type":21},{"name":69,"class":38},{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":4,"eligibilityCriteria":99,"healthyVolunteers":11,"sex":16,"minAge":100,"maxAge":18,"enrollmentInfo":101,"targetDuration":4,"studyType":50,"phases":103,"briefSummary":104,"conditions":105,"keywords":106,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":39},"100510139","using-mukbang-to-improve-appetite-nutritional-status-and-quality-of-life-in-children-with-cancer-100510139","NCT05922553","Using Mukbang to Improve Appetite, Nutritional Status and Quality of Life in Children With Cancer","The Effectiveness of Mukbang in Helping Children With Cancer Hospitalized for Radiotherapy and Chemotherapy to Improve Appetite, Nutritional Status and Quality of Life: A Randomized Control Trial","Inclusion Criteria:\n\n* Aged between 6 to 18 years old;\n* Children in accordance with the guidelines for the Diagnosis and Treatment of 12 Diseases related to hematologic diseases and malignant tumors (2021 version) issued by the General Office of the National Health Commission;\n* At least experience one full cycle of chemotherapy;\n* Children with moderate or higher symptoms of decreased appetite were screened for a list of treatment-related symptoms.\n\nExclusion Criteria:\n\n* Children with serious cardiopulmonary disease, infection, organ damage, or genetic metabolic disease, immune deficiency disease, mental illness;\n* Children with eye or ear dysfunction that prevents them from watching and listening to videos.","6 Years",{"count":102,"type":21},124,[52],"This study aims to use a two arms randomized clinical trial study to evaluate the effectiveness of the effective constituent of Mukbang in helping children with cancer hospitalized for radiotherapy and chemotherapy to improve their appetite, nutritional status and quality of life.",[26],[107,108,109,110,111],"Childhood Cancer","Mukbang","Appetite","Nutritional Status","Quality of Life","2025-07-31",{"date":114,"type":31},"2025-08-06",{"date":116,"type":31},"2024-12-16",{"date":118,"type":21},"2026-06",{"name":120,"class":38},"Wei XIA, PhD"]