[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"adaptive-behavior\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:adaptive-behavior":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,87],{"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":32,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100492002","psychoeducation-of-parents-to-children-with-fasd-100492002",false,"NCT05686473","Psychoeducation of Parents to Children With FASD","Evaluation of a Treatment Program Based on Psychoeducation of Parents of Children and Adolescents With Fetal Alcohol Spectrum Disorder (FASD)","NorFASDPEdu","All children and adolescents (age 2,5-18 years) referred to the Regional Competence Centre for children with prenatal alcohol exposure in Arendal, Norway will be invited to participate in the current research project.\n\nInclusion criteria:\n\n* Valid information about alcohol exposure in fetal life. Exceptions to this inclusion criterion are children who have been adopted and with dysmorphic features that are consistent with full Fetal Alcohol Syndrome.\n\nExclusion Criteria:\n\n* Children with known genetic syndromes, progressive brain and neuromuscular diseases or major sensory defects (blindness or deafness).","ALL","2 Years","18 Years",{"count":21,"type":22},75,"ESTIMATED","INTERVENTIONAL",[25],"NA","By longitudinal, prospective research in children and adolescents with Fetal Alcohol Spectrum Disorders (FASD) and their parents to explore the beneficial effects of participating in a standardized intervention program in order to treat and reduce the consequences of early brain damage. By using elements from international programs based on psychoeducation and parent training, the investigators aim to help parents to better understand and respond to the neurodevelopmental disabilities of their children, and thereby improving behavioral problems and self-regulation deficits.",[28,29,30,31],"Fetal Alcohol Spectrum Disorders","Behavior Problem","Adaptive Behavior","Learning Disorders",[33,34,35,36],"FASD","Psychoeducation","Parenting","Information program","RECRUITING","2025-05-16",{"date":40,"type":41},"2025-05-21","ACTUAL",{"date":43,"type":41},"2025-05-01",{"date":45,"type":22},"2026-12",{"name":47,"class":48},"Sorlandet Hospital HF","OTHER_GOV",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":58,"sex":17,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":23,"phases":63,"briefSummary":64,"conditions":65,"keywords":70,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":49},"100580019","effects-of-music-and-storytelling-on-linguistic-socioemotional-and-adaptive-development-in-children-aged-12-36-months-an-intervention-protocol-in-municipal-early-childhood-centers-100580019","NCT06831851","Effects of Music and Storytelling on Linguistic, Socioemotional, and Adaptive Development in Children Aged 12-36 Months: an Intervention Protocol in Municipal Early Childhood Centers","The Influence of Music and Storytelling on the Linguistic, Socioemotional, and Adaptive Development of Children Aged 12-36 Months: an Intervention Protocol in an Enriched Environment Conducted in Municipal Early Childhood Education Centers (CMEIs)","MUS-STORY","Inclusion Criteria:\n\nChildren of both sexes, aged between 12 and 36 months. Enrolled full-time in Municipal Early Childhood Education Centers (CMEIs). Attending with a daily workload of 10 hours, five days a week.\n\nExclusion Criteria:\n\nDiagnosis of atypical neurodevelopment. Use of sedative or stimulant medications for memory. Undergoing physical therapy for the locomotor system. Presence of any clinical or functional condition that prevents participation. More than five consecutive absences from the intervention program.",true,"12 Months","36 Months",{"count":62,"type":22},16,[25],"This randomized clinical trial aims to evaluate the impact of a structured enriched environment on the linguistic, adaptive behavior, and socioemotional development of children aged 12 to 36 months. The study addresses two main questions:\n\nDoes the intervention improve linguistic, adaptive behavior, and socioemotional development compared to standard care? Does parental guidance amplify the benefits of the intervention?\n\nParticipants will be randomly assigned to one of two groups:\n\nIntervention Group:\n\nChildren will participate in musical activities twice per week (singing, exploring simple instruments, and musical games) and daily storytelling sessions using interactive and visual aids.\n\nWithin this group, parents in the \"with guidance\" subgroup will attend biweekly meetings to learn strategies for reinforcing the intervention at home, while the \"without guidance\" subgroup will not include parental training.\n\nControl Group:\n\nChildren will receive standard care complemented by alternative artistic and pedagogical activities (e.g., drawing, painting), without the structured intervention.",[66,30,67,68,69],"Child Development","Early Child Development","Music Education","Preschool Education",[71,72,73,74,75],"Environmental enrichment","Child development","Early childhood education","Adaptive behavior","Randomized clinical trial","NOT_YET_RECRUITING","2025-03-24",{"date":79,"type":41},"2025-03-26",{"date":81,"type":22},"2025-06-02",{"date":83,"type":22},"2025-11",{"name":85,"class":86},"Universidade Federal de Pernambuco","OTHER",{"id":88,"slug":89,"hasResults":11,"nctId":90,"briefTitle":91,"officialTitle":91,"acronym":4,"eligibilityCriteria":92,"healthyVolunteers":11,"sex":17,"minAge":19,"maxAge":93,"enrollmentInfo":94,"targetDuration":4,"studyType":23,"phases":96,"briefSummary":97,"conditions":98,"keywords":102,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":119,"completionDateStruct":121,"leadSponsor":123,"locationsCount":49},"100374148","health-psychological-group-rehabilitation-for-patients-with-chronic-fatigue-syndrome-mecfs-100374148","NCT04151693","Health Psychological Group Rehabilitation for Patients With Chronic Fatigue Syndrome (ME\u002FCFS)","Inclusion Criteria:\n\n* Clinical diagnosis of Chronic fatigue syndrome, G 93.3\n* Must be able to sit two hours and do homework tasks\n* Must be motivated to co-operate with other patients\n* Goal oritentation\n* Have an interest to learn health psychological approach and willingness to participate rehabilitation\n\nExclusion Criteria (diseases without treatment\u002F acute phase):\n\n* hypothyroidism\n* sleep apnea or narcolepsy\n* major depressive disorders, bipolar affective disorders, schizophrenia\n* eating disorders\n* cancer\n* autoimmune disease\n* hormonal disorders\n* subacute infections\n* obesity\n* alcohol or substance abuse\n* vitamin D deficiency","65 Years",{"count":95,"type":22},80,[25],"Chronic fatigue syndrome (ME\u002FCFS) is a severe medical condition. It is characterized by long term fatique and other persisted symptoms, such as a cognitive disabilities and orthostatic intolerance. Symptoms limit a persons ability to carry out ordinary daily activities. In ICD- 10, disease is known as G93.3, postviral fatigue syndrome.\n\nThe purpose of this research (doctoral study) is to produce a health psychological group intervention for patients with ME\u002FCFS.\n\nResearch protocol: 70-80 patients with diagnosis G 93.3. Psychological and psychiatric evaluation for patients (SCID I and parts from SCID II). Depression diagnosis is allowed (on remission). Medication for depression is also allowed. Measurements for ortostatic intolerance (Somnotouch nimbTM) and laboratory measurements: complete blood count, CRP, alkaline phosphatase, GT, ALAT, CK, bilirubin, kidney and thyroid (TSH, T4V) function tests, serum ferritin, glucose, electrolytes and daily urine sodium excretion.\n\nAutonomic nervous system ganglio antibodies: Anti-AT1R- Antibodies, Anti- ETAR- Antibodies, anti alpha-1 adrenergic Receptor Antibodies, anti alpha 2 adrenergic Receptor Antibodies, anti beta-1 adrenergic Receptor Antibodies, anti beta-2-adrenergic Receptor Antibodies, anti- Muscarinic Cholinergic Receptor 1 (M1)- Antibodies, anti- Muscarinic Cholinergic Receptor 2 (M2)- Antibodies, anti- Muscarinic Cholinergic Receptor 3 (M3)- Antibodies, anti- Muscarinic Cholinergic Receptor 4 (M4)- Antibodies, anti- Muscarinic Cholinergic Receptor 5 (M5)- Antibodies.",[99,100,30,101],"Psychological Adaptation","Cognitive Change","Functioning",[103,104,105,106,107,108,109,110,111,112,113,114,115],"Psychological intervention","Cognitive Behavioral Therapy (CBT)","Accept and Commitment Therapy (ACT)","Cognitive functioning","Fatigue","Autonomic nervous system","Autonomic nervous system ganglio antibodies","Deep breathing","Relaxation","Health care system","Agency","Health psychology","Pacing","2024-04-02",{"date":118,"type":41},"2024-04-03",{"date":120,"type":41},"2019-11-30",{"date":122,"type":22},"2028-05-31",{"name":124,"class":86},"Joint Authority for Päijät-Häme Social and Health Care"]