[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"adolescent---emotional-problem\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:adolescent---emotional-problem":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,52,82,109,146,174,202,226,253],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":33,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100611437","randomized-controlled-trial-of-a-family-focused-intervention-for-caregivers-and-young-adolescents-phase-3-of-flourish-100611437",false,"NCT07240571","Randomized Controlled Trial of a Family-focused Intervention for Caregivers and Young Adolescents (Phase 3 of FLOURISH)","Family-Focused Adolescent & Lifelong Health Promotion: Prevention of Adolescent Mental Health Problems in Eastern Europe","FLOURISH","Inclusion Criteria:\n\n* For Caregivers:\n\nMust be 18 years or older at baseline assessment\n\nMust be the primary caregiver of an adolescent aged 10-14 who has resided in the same household for at least four nights a week in the past month\n\nMust be able to speak at least one of the local languages in which the program will be offered (e.g., Macedonian, Romanian, Russian, Ukrainian or Albanian)\n\nMust agree to participate in the program and provide informed consent for both themselves and their adolescent\n\nFor Adolescents:\n\nMust be aged 10-14 at the baseline assessment\n\nMust provide assent to participate in the study\n\nMust have caregiver consent to participate.\n\nExclusion Criteria:\n\n* No formal exclusion criteria have been established for the FLOURISH project. However, during the study introduction, the research team will guide participants through a consent form that asks whether they are currently experiencing acute distress or a mental or physical health condition that could interfere with participation. The decision to participate will be made by the individual. If a potential participant indicates they are unable to take part due to acute health issues, the research team will provide appropriate referrals to other services.",true,"ALL","10 Years","14 Years",{"count":22,"type":23},1280,"ESTIMATED","INTERVENTIONAL",[26],"NA","The aim of this study is to conduct a multi-country randomized waitlist controlled trial to evaluate the effectiveness, cost-effectiveness, and scalability of the optimized Parenting for Lifelong Health (PLH) for Parents and Teens program in Moldova and North Macedonia. In Phase 2 of the FLOURISH project, a factorial trial tested multiple intervention components and identified the optimized intervention package. In Phase 3, this trial will assess the implementation, outcomes, and economic impact of the optimized PLH program delivered to adolescents aged 10-14 and their caregivers. ALTERNATIVA will deliver the program in North Macedonia and the Health for Youth Association in the Republic of Moldova.",[29,30,31,32],"Adolescent - Emotional Problem","Parent Child Relationship","Family Functioning","Well-Being, Psychological",[34,35,36,37,38],"Multiphase Optimization Strategy (MOST)","Family-based intervention","Adolescents","Mental health","Randomized trial","RECRUITING","2026-05-28",{"date":42,"type":43},"2026-06-02","ACTUAL",{"date":45,"type":43},"2025-10-24",{"date":47,"type":23},"2026-11-30",{"name":49,"class":50},"University of Klagenfurt","OTHER",2,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":18,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":24,"phases":63,"briefSummary":64,"conditions":65,"keywords":68,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":81},"100423713","parent-intervention-for-psychiatrically-hospitalized-youth-100423713","NCT04797455","Parent Intervention for Psychiatrically-Hospitalized Youth","Pilot Intervention for Parents of Psychiatrically-Hospitalized Youth","Inclusion criteria are:\n\n* youth is currently hospitalized on the Stanford unit at Mills Peninsula Medical Center, on the Inpatient Adolescent Psychiatry Unit, for suicidal ideation and\u002For a suicide attempt.\n* youth is between the ages of 12-18 (18 year-old youth must still be in high school and living at home with parents for the duration of the study)\n* at least one parent\u002Fguardian is willing to participate in the study intervention\n* youth and parent speak English well enough to complete study treatment and assessments in English\n\nExclusion criteria are:\n\n• the youth or parent has a psychiatric or medical condition that would interfere with their ability to participate in study assessments and\u002For treatment (such as acute psychosis, neurological impairment, malnutrition due to anorexia)","12 Years","85 Years",{"count":62,"type":23},40,[26],"The purpose of the present study is to conduct a pilot randomized clinical trial (RCT) of a parent coaching intervention for parents of youth hospitalized for suicidal ideation, suicide attempt(s), or non-suicidal self-injury. Parents will receive either the parent coaching intervention (which includes safety planning and behavioral parenting skills training with a clinician and assistance with linkage to follow-up care by a case manager) or treatment as usual (TAU) for the inpatient unit. The long-term goal of the research is to determine if augmenting standard inpatient treatment with additional parenting intervention improves youth treatment response on suicide-related outcomes (i.e., suicidal ideation, non-suicidal self-injury, and suicide attempts). The goal of this pilot RCT is to collect preliminary data needed for a larger RCT, including feasibility, acceptability, safety, tolerability, engagement of the presumed mechanism of change (changes in parent emotions and behaviors), and signal detection of any changes in youth suicide-related outcomes.",[29,66,67],"Suicide and Self-harm","Parenting",[69,70,71],"suicide","Self-Injurious Behavior","Behavioral Symptoms","2026-04-23",{"date":74,"type":43},"2026-04-29",{"date":76,"type":43},"2023-05-01",{"date":78,"type":23},"2026-06-01",{"name":80,"class":50},"Stanford University",1,{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":18,"minAge":59,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":91,"phases":4,"briefSummary":92,"conditions":93,"keywords":95,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":4},"100624629","research-on-disease-control-and-mental-health-status-of-adolescent-asthma-patients-100624629","NCT07412119","Research on Disease Control and Mental Health Status of Adolescent Asthma Patients","Inclusion Criteria:\n\n* Meet the asthma diagnostic criteria of GINA 2025\n* Age 12 to 18 years old\n* The parents and the child patient agreed and filled out the questionnaire completely.\n\nExclusion Criteria:\n\n* Children with other respiratory diseases such as bronchiectasis, bronchiolitis, cystic fibrosis and pneumonia\n* Combined with chronic diseases of other systems","18 Years",{"count":90,"type":23},460,"OBSERVATIONAL","Background: Currently in China, adolescent asthma care is characterized by both undertreatment and overtreatment. Patients in this age group may exhibit negative emotions toward disease treatment and long-term control. Insufficient disease knowledge, irregular lifestyle habits, and negative attitudes toward the disease can all reduce medication adherence, affect disease control outcomes, and thereby increase the risk of severe chronic respiratory conditions and disease burden in adulthood.\n\nObjectives: To assess disease control status in adolescent asthma patients, evaluate the psychological well-being of patients and their family members, and understand patients' self-management skills and readiness for transition to adulthood.\n\nProcedures: Eligible participants will complete a series of assessment questionnaires through the Youran Huxi mobile application, including questionnaires on asthma control, physical activity, psychological health, self-management behaviors, and transition readiness. The study period is 12 months; the baseline assessment involves one-time completion of written questionnaires with no interim follow-up visits. The study does not intervene in clinical diagnosis or treatment decisions.",[94,29],"Asthma (Diagnosis)",[96,97,98],"Asthma","adolescent","mental health","NOT_YET_RECRUITING","2026-02-12",{"date":102,"type":43},"2026-02-17",{"date":104,"type":23},"2026-04-01",{"date":106,"type":23},"2027-12-01",{"name":108,"class":50},"Beijing Children's Hospital",{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":115,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":18,"minAge":117,"maxAge":118,"enrollmentInfo":119,"targetDuration":4,"studyType":91,"phases":4,"briefSummary":121,"conditions":122,"keywords":129,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":139,"completionDateStruct":141,"leadSponsor":143,"locationsCount":145},"100472072","childrens-bipolar-network-treatment-trial-i-100472072","NCT05427123","Children's Bipolar Network Treatment Trial I","A Collaborative Treatment Network for Youth With or at High Risk for Bipolar Disorder","CBN","Inclusion Criteria:\n\n* Youth 9-19 years old\n* Youth diagnosed with Bipolar disorder (I, II, Other Specified) or Cyclothymic Disorder by the study team during the diagnostic interview screening\n* Youth is able to read and communicate in English to the degree necessary to be able to assent and participate (with help) in their treatment and assessments appropriate for ages 9 and up\n* Youth has a caregiver able to participate in ongoing basis in assessment and treatment\n* The participating caregiver can reliably read and communicate in English for purposes of study consenting, assessment, and treatment, unless preferred language translation services are regularly available.\n\nExclusion Criteria:\n\n* Youth has DSM-5 diagnosis of autism spectrum disorder\n* Youth has DSM-5 diagnosis of substance or alcohol abuse with impairment within 3 mos.\n* Youth has a medical or psychiatric disorder that is life-threatening or requires immediate hospitalization or emergency medical or therapeutic treatment\n* Evidence of recent sexual or physical abuse of the youth by legally responsible caregivers\n* Evidence of recent intimate partner violence between caregivers responsible for the youth's care","9 Years","19 Years",{"count":120,"type":23},80,"This is a naturalistic treatment and follow-up study of youth with bipolar spectrum disorders (BSDs) across four US sites of The Childhood Bipolar Network (CBN). CBN sites have expertise in diagnosing, assessing, and treating BSDs in youth. The primary aims of this study are to (1) identify and reliably diagnose youth (ages 9 to 19 yrs) with full bipolar disorder (BD) and BSDs, and (2) examine predictors (e.g., mood instability, inflammatory marker C-reactive protein) of clinical outcome over a 12 month period. Participating youth will initially complete a screening that includes a structured diagnostic interview and a baseline blood draw to measure inflammatory processes. Youth with BSD and parents (80 families) will be asked to participate in multiple follow up research visits with interviews, rating instruments, and questionnaires. Per established CBN guidelines, study psychiatrists will provide and track medication management and sites will also track psychosocial treatments. This study ultimately aims to further understanding of best practice pediatric BSD psychiatric and psychosocial treatments and development of a standardized and validated set of clinical tools for patient assessment, diagnosis, and tracking.",[123,124,125,126,127,128,29],"Bipolar Disorder","Bipolar I Disorder","Bipolar II Disorder","Other Specified Bipolar and Related Disorder","Mood Instability","Child Mental Disorder",[130,131,132,133,134,135],"medication","psychosocial","treatment","longitudinal","naturalistic","assessment","2026-02-02",{"date":138,"type":43},"2026-02-05",{"date":140,"type":43},"2022-07-01",{"date":142,"type":23},"2027-07-01",{"name":144,"class":50},"University of California, Los Angeles",4,{"id":147,"slug":148,"hasResults":11,"nctId":149,"briefTitle":150,"officialTitle":151,"acronym":152,"eligibilityCriteria":153,"healthyVolunteers":11,"sex":18,"minAge":154,"maxAge":4,"enrollmentInfo":155,"targetDuration":4,"studyType":24,"phases":157,"briefSummary":158,"conditions":159,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":81},"100535159","teachers-leading-the-front-lines---adolescent-100535159","NCT06248203","Teachers Leading the Front Lines - Adolescent","Teachers Delivering Task-Shifted Mental Health Care to Adolescents in India","TeaLeaf-A","Inclusion Criteria:\n\nSchools:\n\n* LCP (Low-Cost Private) Secondary Schools\n* Enrolled families earning \\\u003C$10 daily\n* Located in greater Darjeeling\n* Principal must also be eligible to participate\n\nPrincipals:\n\n* \\>18 years old\n* Employed at enrolled school\n* Not suspected or convicted of child maltreatment\n\nTeachers:\n\n* \\>18 years old\n* Employed at enrolled school\n* Not suspected or convicted of child maltreatment\n\nStudents:\n\n* Age 13 - 17 years\n* Student of enrolled teacher\n* Borderline or clinical Total Problem or subscale score of YSR (Youth Self-Report) and TRF (Teacher's Report Form)\n* Each student has a lead teacher (2\u002Fteacher), with their other teachers also involved\n\nGuardians\n\n* \\>18 years old\n* Guardian of enrolled student\n* Not suspected or convicted of child maltreatment\n\nExclusion Criteria:\n\n* Exclusion criteria will be set as each participant not meeting inclusion criteria as set for their group.","13 Years",{"count":156,"type":23},216,[26],"Purpose: The purpose of this research is to pilot test a novel, alternative, potentially sustainable system of teacher-delivered, task-shifted adolescent mental health care.\n\nParticipants: Principals of 60 rural, low-cost private secondary schools of the Darjeeling Himalayas will be invited to participate as a school and an individual. Teachers will be approached individually. Two students per teacher who meet inclusion criteria will be randomly chosen for enrollment.\n\nProcedures: This is a RE-AIM (Reach, Effectiveness, Adoption, Implementation, Maintenance) guided, mixed methods CRCT, clustered at schools, of Tealeaf-A's Reach, Adoption \\& Implementation (Primary Outcomes, implementation-based), as well as evaluating for preliminary indicators of Effectiveness \\& Maintenance (Secondary Outcomes, clinically-based).",[160,29,161,162,163,164],"Adolescent Behavior","Mental Health Issue","Psychosocial Functioning","Depression","Anxiety","2025-12-16",{"date":167,"type":43},"2025-12-18",{"date":169,"type":43},"2024-02-29",{"date":171,"type":23},"2027-02-01",{"name":173,"class":50},"University of North Carolina, Chapel Hill",{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":11,"sex":18,"minAge":154,"maxAge":181,"enrollmentInfo":182,"targetDuration":4,"studyType":24,"phases":184,"briefSummary":185,"conditions":186,"keywords":188,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":193,"lastUpdatePostDateStruct":194,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":200,"locationsCount":81},"100556966","effectiveness-of-a-digital-application-for-adolescents-with-mild-to-moderate-anxiety-100556966","NCT06531980","Effectiveness of a Digital Application for Adolescents With Mild to Moderate Anxiety","Effektiviteten av en Digital Mestringsapp for Ungdommer Med Mild Til Moderat Angst","Inclusion Criteria:\n\n* Ages 13-16\n* Resides in Bergen\n* Completed RCADS-25\n* Reports \"yes\" to both questions:\n* Do you have anxiety symptoms? Do you often feel stressed, scared, worried, or feel it in your body (e.g., stomach pain, heart palpitations, breathing problems, sweating, dizziness)?\n* Do anxiety symptoms prevent you from doing things you want or need to do (e.g., meeting new people, giving presentations at school, going to sleepovers, going to the shopping center)? Or do you spend so much time worrying that it affects your daily life? Can read Norwegian\n\nExclusion Criteria:\n\n* Currently receiving other psychological treatment\n* Immediate need for other psychological treatment, such as severe depression, suicide risk, OCD, psychosis\u002Fsubstance abuse issues, autism spectrum disorder\n* Anxiety is largely related to bullying\n* Extensive school absence of more than 50% in the last three months","16 Years",{"count":183,"type":23},128,[26],"The goal of this randomized controlled trial is to investigate the effectiveness of a new therapist-guided rule based intervention in Bergen Municipality, Child and Family help center.\n\nDo they have a decrease in anxiety symptoms following the intervention? Do they have an increase in functional level following the intervention?\n\nResearchers will compare the therapist-guided rule based intervention with treatment as usual for adolescents with mild to moderate anxiety.\n\nParticipants will use the intervention, which is based on CBT, for 8 weeks.",[164,187,29],"Anxiety and Fear",[189,190,191,97,192],"Digital Health","Digital interventions","Cognitive behavior therapy","anxiety","2025-08-22",{"date":195,"type":43},"2025-08-28",{"date":197,"type":43},"2025-01-16",{"date":199,"type":23},"2026-12-30",{"name":201,"class":50},"Haukeland University Hospital",{"id":203,"slug":204,"hasResults":11,"nctId":205,"briefTitle":206,"officialTitle":206,"acronym":4,"eligibilityCriteria":207,"healthyVolunteers":11,"sex":18,"minAge":208,"maxAge":88,"enrollmentInfo":209,"targetDuration":4,"studyType":24,"phases":211,"briefSummary":212,"conditions":213,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":223,"locationsCount":225},"100454654","equine-assisted-therapy-for-therapy-resistant-adolescents-with-autism-spectrum-disorders-a-replicated-ab-design-100454654","NCT05200351","Equine-assisted Therapy for Therapy-resistant Adolescents With Autism Spectrum Disorders, a Replicated AB-design","Inclusion Criteria:\n\n* between 11-18 years old;\n* a clinical diagnosis of autism spectrum disorders according the Diagnostic and Statistical Manual of Mental Disorders 5 (DSM 5) as diagnosed by a Beroepen in de Individuele Gezondheidszorg (BIG) registered healthcare professional;\n* insufficient emotion regulation after regular therapy for at least 1,5 years as indicated by a score above clinical cut-off (T-score = 65) on the EDI;\n* comorbidities are allowed except for those interfering with safety.\n\nExclusion Criteria:\n\n* unable to respond to questions (parents or adolescents);\n* no access to an Internet connection;\n* insufficient mastery of Dutch language in parents or adolescents;\n* physically incapable to work with the horses;\n* unstable medication use;\n* total intelligence quotient (IQ) equal to or below 80 on the Wechsler Intelligence Scale for Children (WISC-III-R or WISC-V);\n* allergic or phobic to horses;\n* insufficient regulation to safely handle the horses;\n* therapy with horses within the last two years.","11 Years",{"count":210,"type":23},35,[26],"The purpose of this study is to assess the (cost)effectivity of Equine assisted Therapy in adolescents with Autism Spectrum disorders.",[214,215,29],"Emotion Regulation","Autism Spectrum Disorder","2024-11-01",{"date":218,"type":43},"2024-11-04",{"date":220,"type":43},"2022-02-14",{"date":222,"type":23},"2024-12",{"name":224,"class":50},"Karakter Kinder- en Jeugdpsychiatrie",3,{"id":227,"slug":228,"hasResults":11,"nctId":229,"briefTitle":230,"officialTitle":231,"acronym":232,"eligibilityCriteria":233,"healthyVolunteers":11,"sex":18,"minAge":59,"maxAge":234,"enrollmentInfo":235,"targetDuration":4,"studyType":24,"phases":237,"briefSummary":238,"conditions":239,"keywords":242,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":245,"startDateStruct":247,"completionDateStruct":249,"leadSponsor":251,"locationsCount":81},"100553711","school-based-treatment-of-social-anxiety-with-developmentally-oriented-cognitive-therapy-for-social-anxiety-disorder-100553711","NCT06489639","School-based Treatment of Social Anxiety With Developmentally Oriented Cognitive Therapy for Social Anxiety Disorder","School-based Treatment of Social Anxiety: A Randomized and Controlled Study Using Developmentally Oriented Cognitive Therapy for Social Anxiety Disorder","SBT-DOCT-SAD","Inclusion criteria:\n\n* age 13-17 years\n* diagnosis of DSM-5 SAD (Social Anxiety Disorder)\n* SAD is the primary mental health disorder\n* motivation of the adolescent and parent to attend DOCT-SAD \u002F SC as described in the study protocol\n* good command of the Finnish language.\n\nExclusion criteria:\n\n* intellectual deficit\n* presence of primary autism spectrum disorder\n* marked psychotic symptoms or psyhotic disorder\n* severe eating disorder, depression or primary other anxiety disorder requiring acute treatment which need to be prioritized above treatment of social anxiety\n* acute suicidality or suicide risk\n* substance use or substance use disorder requiring child protection measures\n* presence of contextual\u002Fenvironmental risk factors in the participants surroundings which require child protection measures","17 Years",{"count":236,"type":23},156,[26],"The goal of this randomized controlled trial is to find out whether the brief, 10-session Developmentally Oriented Cognitive Therapy for Social Anxiety Disorder (DOCT-SAD) is more effective than standard counseling (SC) to treat Social Anxiety Disorder (SAD) among 12 to 17-year-old adolescents with SAD.\n\nPotential participants for the study are identified from school health and well-being services (SHWS). The DOCT-SAD is delivered by method-trained school psychologists working in the SHWS. SC will be provided by non-method-trained SHWS professionals (i.e. school nurses, social workers or school psychologists) according to their routine counselling practice.\n\nThe main research questions of the study are:\n\n1. Is DOCT-SAD more effective than SC for alleviating symptoms of social anxiety?\n2. Is DOCT-SAD more effective than SC to produce diagnostic remission from primary SAD and alleviating symptom severity associated with SAD?\n3. Is DOCT-SAD more effective than SC for alleviating co-occurring depressive symptoms, interference in daily functioning due to worry or fears, and for increasing general well-being, positive mental health, and for improving the quality of life among adolescents with SAD?\n\nResearchers will compare DOCT-SAD with SC to see if DOCT-SAD is effective in the treatment of SAD in adolescents.\n\nParticipants will:\n\n* be treated either with DOCT-SAD or SC for 10 weeks.\n* be followed up and assessed clinically at six-month and twelve-month follow-up points.",[240,241,29],"Social Anxiety Disorder","Social Anxiety",[243],"social anxiety, adolescents, cognitive behavioural therapy","2024-06-28",{"date":246,"type":43},"2024-07-08",{"date":248,"type":43},"2023-03-20",{"date":250,"type":23},"2028-12-31",{"name":252,"class":50},"Klaus Ranta",{"id":254,"slug":255,"hasResults":11,"nctId":256,"briefTitle":257,"officialTitle":258,"acronym":259,"eligibilityCriteria":260,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":181,"enrollmentInfo":261,"targetDuration":4,"studyType":91,"phases":4,"briefSummary":263,"conditions":264,"keywords":270,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":282,"lastUpdatePostDateStruct":283,"startDateStruct":285,"completionDateStruct":287,"leadSponsor":289,"locationsCount":291},"100479667","vulnerabilityresilience-factors-influencing-the-developmental-trajectories-and-adaptive-methods-of-children-and-adolescents-in-child-welfare-system-100479667","NCT05525962","Vulnerability\u002FResilience Factors Influencing the Developmental Trajectories and Adaptive Methods of Children and Adolescents in Child Welfare System.","Facteurs de vulnérabilité\u002Frésilience influençant Les Trajectoires développementales et Les modalités Adaptatives d'Enfants et d'Adolescents confiés à l'Aide Sociale à l'Enfance. Cohorte Primo-arrivants.","EvolASE-PEA","Inclusion Criteria:\n\n* Minor adressed to child protective services\n* Minor placed full time\n\nExclusion Criteria:\n\n* Non affiliation to social security system\n* Non accompanied minor\n* Minor and\u002For parfents not understanding french\n* Minor informed and refused participation\n* Parents or tutor having refused participation of their child",{"count":262,"type":23},300,"Assess the prevalence of medico-psychological characteristics at the time of placement (M0), their appearance \u002F disappearance and during the two years following placement (M12 and M24) by age group in children \u002F adolescents in Child Protective Services and placed full-time in the structures of Seine-Maritime and Eure as well as in nursery in Le Havre or Rouen",[265,266,267,268,160,128,269,29],"Behavior, Child","Child Development","Child Development Disorder","Adolescent Development","Child Behavior Disorders",[271,272,97,273,274,275,276,277,278,279,280,281],"child","preschool","psychiatry","psychology","Child Protective Services","social sciences","child protection","social services","psychiatric disorders","attachement","developmental trajectories","2024-04-08",{"date":284,"type":43},"2024-04-09",{"date":286,"type":43},"2022-09-29",{"date":288,"type":23},"2027-09-29",{"name":290,"class":50},"University Hospital, Rouen",5]