[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"family-relations\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:family-relations":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,45,72,101,130,166,190,216,241],{"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":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100611844","evaluation-of-a-family-centered-program-for-problematic-gamingexcessive-screen-use-100611844",false,"NCT07245862","Evaluation of a Family-centered Program for Problematic Gaming\u002FExcessive Screen Use","Evaluation of a Family-centered Program for Problematic Gaming\u002FExcessive Screen Use in a Child and Adolescent Population Within Social Services in Light of the New Social Services Law","S-FAME","Inclusion Criteria:\n\n* family conflicts related to screen use\n* spaeks and udnerstand swedish\n\nExclusion Criteria:\n\n* se above","ALL","11 Years","14 Years",{"count":21,"type":22},170,"ESTIMATED","INTERVENTIONAL",[25],"NA","The Family-Centered Program for Problematic Gaming and Excessive Screen Use (FAME) is a pioneering initiative designed to address the growing challenges of excessive screen use and gaming among children and adolescents, particularly within family dynamics.",[28,29,30,31],"Adolescent Behavior","Social Media Addiction","Gaming Disorder","Family Relations","RECRUITING","2026-04-24",{"date":35,"type":36},"2026-04-30","ACTUAL",{"date":38,"type":36},"2026-01-01",{"date":40,"type":22},"2028-01-01",{"name":42,"class":43},"Region Skane","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":23,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":71},"100475974","impacts-of-cash-transfers-on-child-neurodevelopment-auxilio-brasil-100475974","NCT05477901","Impacts of Cash Transfers on Child Neurodevelopment (Auxilio Brasil)","Mental Health and Bolsa Familia: A Mechanistically Focused Clinical Trial of a Cash Transfer Intervention on Child Brain, Behavior, and Mental Health","Mother:\n\nInclusion Criteria:\n\n1. Age 23-45 years old\n2. Receiving AB cash transfers\n3. Has at least two or more children ages 7- 10 years old at time of recruitment (up to 4 children per family)\n4. Able to consent\n\nExclusion Criteria:\n\n1\\. Mother and child do not reside in same household\n\nChild:\n\nInclusion Criterion\n\n1. Age 7-10 years old\n2. Intellectual Disability\n\nExclusion Criterion\n\n1. Does not reside in same household as the mother\n2. Major Axis I disorder (e.g., Autism, Schizophrenia, Bipolar)\n3. Severe Disability\n4. MRI contradictions (index child only)","23 Years","45 Years",{"count":55,"type":22},450,[25],"This study examines the impact of Auxilio Brasil (AB), a cash transfer program to mothers of school-age children, on resource-deprived populations in Brazil and its protective effects on child neurodevelopment and mental health. The investigators will conduct a randomized clinical trial (RCT) among those already receiving AB in which 300 families will be randomized in a 1:1 ratio to receive either a high ($40\u002Fmonth) or low ($2\u002Fmonth) supplemental transfer for 2 years. Three hundred children (index child participants; 7-10 years old) will be enrolled across both study arms. Additionally, up to 150 siblings (\"sibling participants;\" 7-10 years old) will be enrolled. Eligible families who decide to participate will sign a study-specific informed consent (mother) and assent (child) form. The UNIFESP team will conduct the respective assessments at baseline, approximately 8- and 16- months, 24-months and approximately 6-months post-RCT.\n\nAim 1: Determine the impact of high vs low cash transfers on children's exposure to adversities (ACEs) and neurodevelopment.\n\nAim 2: Determine the impact of cash transfers on children's inflammatory markers and HPA activity\u002Fcortisol.\n\nExploratory Aim: The investigators will explore (i) whether sex\u002Fgender of the children moderates the pathways in the above mediation model; and (ii) whether cash transfer-related effects persist 6 months post-RCT.",[59,60,61,31],"Inflammation","HPA","CBCL","2026-04-20",{"date":64,"type":36},"2026-04-23",{"date":66,"type":36},"2025-05-28",{"date":68,"type":22},"2029-01-31",{"name":70,"class":43},"New York State Psychiatric Institute",2,{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":4,"eligibilityCriteria":78,"healthyVolunteers":79,"sex":17,"minAge":80,"maxAge":4,"enrollmentInfo":81,"targetDuration":4,"studyType":23,"phases":82,"briefSummary":83,"conditions":84,"keywords":87,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":44},"100603403","jockey-club-support-project-100603403","NCT07136064","Jockey Club Support Project","Jockey Club Support Project to Enhance Emotion Regulation Skills and Resilience of Cross-Boundary Families: A Randomized Controlled Trial","Inclusion Criteria for Parents:\n\n1. have at least one child between the fifth and twelfth grade;\n2. can participate in the intervention with their child;\n3. are Hong Kong residents or have a family member who is a Hong Kong resident;\n4. live in Shenzhen.\n\nInclusion Criteria for Children:\n\n1. are between the fifth and twelfth grade;\n2. are Hong Kong residents or have a family member who is a Hong Kong resident;\n3. live in Shenzhen.\n\nExclusion Criteria:\n\n(a) those who have current diagnoses of severe physical or mental illnesses;",true,"10 Years",{"count":55,"type":22},[25],"Guided by the process model of emotion regulation, integrative affect-regulation framework for resilience, and the reciprocal dynamics of emotion, affect, and resilience in the family system, researchers will develop a parallel intervention to incorporate two key members in Mainland-Hong Kong cross-boundary families: a parent and a child by improving their affect\u002Femotion regulation skills, de-escalate family conflicts, and flourish under hardships. Specifically, researchers predict that participants in the intervention group will report greater improvement in resilience, emotion regulation, psychological well-being, family harmony, and social connectedness than those in the control group.",[31,85,86],"Resilience","Emotion Regulation",[88,89,90,91],"cross-boundary families","resilience","emotion regulation","randomized controlled trial","2026-02-10",{"date":94,"type":36},"2026-02-12",{"date":96,"type":36},"2025-11-15",{"date":98,"type":22},"2028-08",{"name":100,"class":43},"City University of Hong Kong",{"id":102,"slug":103,"hasResults":11,"nctId":104,"briefTitle":105,"officialTitle":106,"acronym":4,"eligibilityCriteria":107,"healthyVolunteers":11,"sex":17,"minAge":108,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":23,"phases":112,"briefSummary":113,"conditions":114,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":44},"100536179","hybrid-type-1-randomized-pilot-trial-of-a-peer-led-family-and-social-strengthening-group-intervention-for-refugee-families-100536179","NCT06261463","Hybrid Type 1 Randomized Pilot Trial of a Peer-led Family and Social Strengthening Group Intervention for Refugee Families","Leveraging Implementation Science and Design Methods to Sustain Community-based Mental Health Services for Refugees","To participate in the study, the families must meet the following criteria:\n\n1. Country of origin: Iraq, Syria, Lebanon, Jordan, Palestine or Yemen\n2. refugee family living in Chicago \\\u003C three years\n3. Contains at least one adult caregiver (18-55) and at least one of their children (age 12 and older) living in one household\n4. One family member with \\> 3 on the GHQ-12\n5. able to give written informed consent.\n\nExclusion criteria for refugee families:\n\n1. Not from one of the following Arabic-speaking countries in the Middle East: Iraq, Syria, Jordan, Lebanon, Palestine, Yemen\n2. men and women who do not have least one child aged 12 years and older living in one household\n3. arrived in the U.S as a refugee greater than 3 years ago\n4. persons with developmental disabilities which would preclude their participation in the adapted CAFES intervention\n5. persons with severe mental health (e.g., suicidality psychotic disorder), active substance use or current in family crisis (e.g., domestic violence, divorce proceedings).","12 Years","55 Years",{"count":111,"type":22},74,[25],"The proposed study draws on prior research to evaluate the feasibility, acceptability and explore preliminary effectiveness of Coffee and Family Education and Support, Version (CAFES2) using a pilot randomized type 1 hybrid effectiveness-implementation design. CAFES2 is a peer-led family and social strengthening multiple family group intervention that is designed to respond to multi-level needs of refugee families. Results of the trial will contribute to the emerging evidence base on family-based mental health interventions for refugee and newcomer communities. The trial will also generate new insights regarding implementation strategies needed to promote successful delivery of services by peer providers and the unique role of human-centered design practices for adaptation of mental health and psychosocial interventions.",[115,116,117,118,119,120,31],"Depression","Anxiety","PTSD","Family Dynamics","Social Functioning","Family Support","2025-09-25",{"date":123,"type":36},"2025-10-01",{"date":125,"type":36},"2024-05-31",{"date":127,"type":22},"2026-08-30",{"name":129,"class":43},"University of Illinois at Chicago",{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":135,"acronym":136,"eligibilityCriteria":137,"healthyVolunteers":79,"sex":17,"minAge":138,"maxAge":139,"enrollmentInfo":140,"targetDuration":4,"studyType":142,"phases":4,"briefSummary":143,"conditions":144,"keywords":149,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":156,"lastUpdatePostDateStruct":157,"startDateStruct":159,"completionDateStruct":161,"leadSponsor":163,"locationsCount":165},"100482089","taiwan-real-world-ldct-screening-behavior-and-outcome-research-for-high-risk-subjects-based-on-health-promotion-administration-100482089","NCT05557487","Taiwan Real-world LDCT Screening Behavior and Outcome Research for High Risk Subjects Based on Health Promotion Administration","Taiwan Real-world Low-dose Computed Tomography Screening behavIor and Outcome Research for High Risk Subjects Based on Health Promotion Administration-part A: Questionnaire Survey -Part B: LDCT Screening Outcome and Management","TRIO","Inclusion Criteria:\n\nGroup 1: Previous heavy smokers Age 50 to 80 years, meet both criteria in the followings.\n\n1. Cigarette smoking of at least 20 pack-years\n2. With successful smoking cessation history (stopping smoking for more than 6 months), but less than 15 years\n\nGroup 2: First-degree relatives of lung cancer patients\n\n1. aged more than 50 years\n2. age less than 50 years old, but older than the age at diagnosis of the youngest lung cancer proband in the family\n\nGroup 3: With other high-risk occupational or environmental factors Age 50 to 80 years, meet one or more of the following criteria.\n\n1. air-pollution exposed occupations (such as traffic policemen, and street cleaners….) for at least 10 years\n2. cooking index ≥ 110, defined as 2\u002F7 \\* days cooking by pan frying, stir-frying, or deep frying in one week \\* years cooking.\n3. cooking without using ventilation for more than 20 years\n4. history of pulmonary tuberculosis and complete anti-tuberculosis treatment with intervals more than 5 years before this study\n\nExclusion Criteria:\n\n1. previous history of lung cancer\n2. another malignancy except for cervical carcinoma in situ or non-melanomatous carcinoma of the skin within 5 years\n3. an inability to tolerate transthoracic procedures or thoracotomy\n4. chest CT examination was performed within 18 months\n5. hemoptysis of unknown etiology within one month\n6. body weight loss of more than 6 kg within one year without an evident cause\n7. a known pregnancy\n8. Not capable of understanding or responding to the written questionnaire even through the help from the study team","20 Years","80 Years",{"count":141,"type":22},6618,"OBSERVATIONAL","Lung cancer is the leading cause of mortality in the world, and also in Taiwan.Despite the researches and availability in new therapies, it causes the highest mortality and is one of the most preventable cancers as well. Smoking is the most common cause of lung cancer worldwide. Compared to lung cancer in smokers, lung cancer in never-smokers is associated with East Asian ethnicity, female sex, and adenocarcinoma histology. This unique risk group is likely to have distinct molecular drivers, especially EGFR, ALK, and ROS1 mutations.In National Taiwan Cancer Registry data, more than half (53%) of all newly diagnosed lung cancer patients and 93% of female patients are lifelong never-smokers. This scenario is common in East Asia. It is essential to develop a different strategy for screening lung cancer patients with other high-risk profiles. Several risk factors have been identified in never-smoking lung cancer and one of the most important factor is a lung cancer family history (LCFH) in a first-degree relative. Other high-risk occupational or environmental factors include air-pollution exposed occupations (such as traffic policeman and street cleaners) for at least 10 years, cooking index ≥ 110, defined as 2\u002F7 \\* days cooking by pan frying, stir frying, or deep frying in one week \\* years cooking, cooking without using ventilation, passive smoke exposure, and history of pulmonary tuberculosis or chronic obstructive pulmonary disorders.\n\nAs described above, three high risk groups are interested in this study, the previous heavy smokers (group 1); those who has family history (group 2) and those who have high risk occupation or environment factors (group 3). From the published researches, we assume the detection rate to be 1.1% for group 1 based on NLST results16, 2.6% for group 2 (395 out of 12,011 subjects in TALENT), and we assume the detection Group 3 to be 1% after consulting board-certified senior specialists in this field.\n\nThis is a prospective, multi-center, single arm study in Taiwan of subjects who are eligible to receive LDCT screening based on recommendation of Health Promotion Administration of Taiwan.\n\nThe primary objective of TRIO part A is the LDCT screening acceptance rate of high lung cancer risk subjects.\n\nThe primary objective of TRIO part B is the exact lung cancer detection rates in these three groups.\n\nOther secondary objectives are also included.",[145,146,147,148,31],"Lung Cancer","High-Risk Cancer","Smoking","Pollution; Exposure",[150,151,152,153,154,147,155],"Lung cancer","Low-dose computed tomography","Real world data","Lung cancer family history","Air pollution","Lung cancer risk questionnaire","2025-09-03",{"date":158,"type":36},"2025-09-10",{"date":160,"type":36},"2022-12-15",{"date":162,"type":22},"2028-12-31",{"name":164,"class":43},"Gee-Chen Chang",7,{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":170,"acronym":4,"eligibilityCriteria":171,"healthyVolunteers":79,"sex":17,"minAge":138,"maxAge":172,"enrollmentInfo":173,"targetDuration":4,"studyType":142,"phases":4,"briefSummary":175,"conditions":176,"keywords":177,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":181,"lastUpdatePostDateStruct":182,"startDateStruct":184,"completionDateStruct":186,"leadSponsor":188,"locationsCount":71},"100596651","specimen-and-clinical-data-collection-plan-for-ldct-screening-participants-100596651","NCT07048236","Specimen and Clinical Data Collection Plan for LDCT Screening Participants","Inclusion Criteria:\n\nPrevious heavy smokers\n\nAccording to The Lung Cancer Early Detection Program in Taiwan:\n\nAdults aged 50 to 74 years with a smoking history of at least 20 pack-years, who are either current smokers or have quit smoking within the past 15 years. Current smokers must agree to participate in a smoking cessation program.\n\nFirst-degree relatives of lung cancer patients\n\nAccording to The Lung Cancer Early Detection Program in Taiwan:\n\nMen aged 45 to 74 years and women aged 40 to 74 years who have a biological parent, child, or sibling diagnosed with lung cancer. Individuals who currently smoke must agree to participate in a smoking cessation program.\n\nExclusion Criteria:\n\n1. Pregnancy\n2. History of chest computed tomography (including low-dose CT) within the past 12 months.\n3. Previous diagnosis of lung cancer\n4. Inability to undergo thoracic biopsy or surgery\n5. Inability to complete the scan procedure, such as due to being unable to hold their breath.\n6. Unexplained hemoptysis within the past month\n7. Chest X-ray within the past month showing a clearly suspicious lung lesion\n8. Unexplained weight loss exceeding 6 kilograms within the past year","74 Years",{"count":174,"type":22},12000,"Lung cancer remains the leading cause of cancer-related mortality in Taiwan and globally, with increasing incidence and the highest healthcare cost burden among cancers in Taiwan. Despite the widespread use of low-dose computed tomography (LDCT) for screening smokers, over half of lung cancer cases in Taiwan occur in never-smokers, highlighting the need for improved risk stratification. Current national LDCT screening programs do not collect comprehensive risk-related data, limiting their predictive accuracy. This project proposes a five-year, multi-center initiative to establish an integrated biospecimen and clinical data collection system. In its first year, a feasibility pilot will be conducted, followed by recruitment of 12,000 participants. Data collection will include biospecimens (blood, urine, tissue), genomic and proteomic analyses, imaging, and detailed questionnaires covering lifestyle, environmental, and occupational exposures. The project will also develop and validate lung cancer prediction models incorporating epidemiologic, biomarker, air pollution, and imaging data. A Common Data Model (CDM) will be implemented to ensure cross-institutional data standardization and support future international collaboration.",[145,147,31],[178,151,153,147,179,180,155],"lung cancer","proteomic","genomic","2025-07-15",{"date":183,"type":36},"2025-07-18",{"date":185,"type":22},"2025-07-17",{"date":187,"type":22},"2034-12-31",{"name":189,"class":43},"Chung Shan Medical University",{"id":191,"slug":192,"hasResults":11,"nctId":193,"briefTitle":194,"officialTitle":195,"acronym":196,"eligibilityCriteria":197,"healthyVolunteers":11,"sex":17,"minAge":80,"maxAge":19,"enrollmentInfo":198,"targetDuration":4,"studyType":23,"phases":200,"briefSummary":201,"conditions":202,"keywords":204,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":207,"lastUpdatePostDateStruct":208,"startDateStruct":209,"completionDateStruct":211,"leadSponsor":213,"locationsCount":215},"100537252","family-intervention-for-black-teens-with-type-1-diabetes-100537252","NCT06275412","Family Intervention for Black Teens With Type 1 Diabetes","Family mHealth Intervention to Improve Health Outcomes in Black Youth With Type 1 Diabetes","3Ms","Inclusion Criteria:\n\n* Age: 10 years, 0 months - 14 years, 11 months\n* Diagnosed with Type 1 diabetes\n* Diagnosed for at least 6 months\n* Black\n* Primary caregiver willing to participate\n* Residence within 30 miles of a recruitment site\n* Caregiver ownership of an Internet-enabled device (cell phone, laptop or desktop computer, tablet, etc)\n\nExclusion Criteria:\n\n* Mental health conditions that might compromise data integrity (e.g., developmental delay, schizophrenia, psychosis, current suicidality, homicidality)\n* Co-morbid medical condition resulting in atypical diabetes management (e.g., cystic fibrosis)\n* Inability to speak or read English\n* Child is in out-of-home placement",{"count":199,"type":22},216,[25],"The purpose of this study is to conduct a multicenter, randomized effectiveness trial of The 3Ms 2.0 compared to an educational control condition for improving adolescent glycemic control and diabetes-related family relationships and reducing primary caregiver diabetes-related distress among Black adolescents with type 1 diabetes (T1D) and their primary caregivers. The proposed study would develop and test The 3Ms 2.0 adapted intervention when delivered using a mobile health approach (accessed via parents' cell phone). The intervention will also include new family intervention content (videoclips and text messages).",[203,31],"Type 1 Diabetes",[203,205,206],"mobile health","Family-based intervention","2025-07-14",{"date":181,"type":36},{"date":210,"type":36},"2024-09-16",{"date":212,"type":22},"2028-04-30",{"name":214,"class":43},"Wayne State University",4,{"id":217,"slug":218,"hasResults":11,"nctId":219,"briefTitle":220,"officialTitle":220,"acronym":4,"eligibilityCriteria":221,"healthyVolunteers":11,"sex":17,"minAge":222,"maxAge":4,"enrollmentInfo":223,"targetDuration":4,"studyType":23,"phases":225,"briefSummary":226,"conditions":227,"keywords":4,"overallStatus":230,"whyStopped":4,"lastUpdateSubmitDate":231,"lastUpdatePostDateStruct":232,"startDateStruct":234,"completionDateStruct":236,"leadSponsor":238,"locationsCount":4},"100562547","the-parental-journey-digital-tool-for-security-in-parenthood-a-way-to-promote-public-health-a-pilot-study-100562547","NCT06604585","The Parental Journey. Digital Tool for Security in Parenthood, a Way to Promote Public Health. A Pilot Study.","Inclusion Criteria:\n\n* Adult parents (or another adult who is a primary caregiver) to children within pediatric healthcare services with children aged 2-5 years old.\n* The parents are not participating in other parental support programs or interventions from Child Health Care psychologists, as this would complicate the evaluation of the effects of each intervention.\n* Parents who speak Swedish, due to the fact that \"Parenting - a journey together\" has not yet been translated into other languages.\n* Parents who respond affirmatively to the inclusion questions, indicating that they perceive a need for additional parental support and are motivated to participate in the program.\n\nInclusion questions for assessing a parent's needs and motivation to participate in the digital parenting support program:\n\n1. How important do you consider your ability\u002Fconfidence as a parent to be for you right now?\n2. What has motivated you to consider participating in this program?\n3. How motivated are you to make changes in your behavior to improve your parenting ability?\n4. Do you have previous experiences with similar digital programs or parental support interventions? If yes, what was your experience?\n5. What type of support do you think you need to successfully complete this program?\n\nExclusion Criteria:\n\n* Parents of children outside the 2-5 years age range. The program is specifically designed for parents within child health care with children in this age group. Once children reach the age of 6, they transition to school health care.\n* The parents who are already participating in other parental support programs or receiving interventions from Child Health Care psychologists are not eligible, as this would complicate the evaluation of the effects of each intervention.\n* Parents who do not speak Swedish, as the program 'Parenting - a Journey Together' has not yet been translated into other languages.\n* Parents who have indicated no perceived need for additional parental support.","18 Years",{"count":224,"type":22},30,[25],"The goal of this randomized clinical pilot study is to evaluate the feasibility and experience of the internet-based parental support program \"Parenting - a journey together\". This program is intended to be delivered via the national Support and Treatment Platform and used within primary care to enhance traditional parental support within child health care when needed. The main questions it aims to answer are:\n\n1. Is the digital parental support intervention feasible and helpful within primary care?\n2. How do parents perceive the program \"Parenting - a journey together\"?\n3. Does the program increase the sense of parental ability and security in parenting by reflecting on attitudes and approaches in interaction with the child?\n\nParticipants in this study will be parents of children aged 2-5 years who have expressed interest in participating in the study and in the parental support program. Participants will be randomized into either the intervention group or the control group. Participants will be asked to complete validated questionnaires measuring the parent-child relationship, perceived parental ability, stress, and well-being before and after the parental support program, and again after 3 months. These results will then be compared with those of the control group.The knowledge gained from the pilot study can contribute to the development of digital parental support interventions within primary care. If the pilot study proves that the interactive digital parenting program is feasible for use in child health centers and is perceived as helpful by parents, a larger randomized controlled (RCT) study, (not included in this application) will be conducted to evaluate its effectiveness.",[228,229,31],"Primary Prevention","Parenting","NOT_YET_RECRUITING","2024-09-17",{"date":233,"type":36},"2024-09-19",{"date":235,"type":22},"2024-11",{"date":237,"type":22},"2026-11",{"name":239,"class":240},"Vastra Gotaland Region","OTHER_GOV",{"id":242,"slug":243,"hasResults":11,"nctId":244,"briefTitle":245,"officialTitle":246,"acronym":247,"eligibilityCriteria":248,"healthyVolunteers":11,"sex":17,"minAge":249,"maxAge":250,"enrollmentInfo":251,"targetDuration":4,"studyType":23,"phases":253,"briefSummary":254,"conditions":255,"keywords":256,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":261,"lastUpdatePostDateStruct":262,"startDateStruct":264,"completionDateStruct":266,"leadSponsor":268,"locationsCount":44},"100540874","dialogical-family-guidance-postdoc-study-100540874","NCT06322511","Dialogical Family Guidance PostDoc Study","The Effectiveness of Dialogical Family Guidance in Families With a Child With Neurodevelopmental Disorders","DFG II","Inclusion Criteria:\n\n* Families with a child with clinical diagnosis within neurodevelopmental ambrella (ADHD, Tourette, Autism disorder, OCD...).\n* the child must be between 4-13 years.\n\nExclusion Criteria:\n\n* Families who do not understand finnish language (because they can not fill the questionnaires and professionals offering DFG are all finnish speaking). At least one parent needs to talk finnish.\n* Families who are not motivated to receive DFG.\n* Families who do not have a child with neurodevelopmental disorders.","4 Years","13 Years",{"count":252,"type":22},50,[25],"This new family intervention, called Dialogical Family Guidance (DFG) is developed to target family needs especially in families with a child with neurodevelopmental disorders. PhD study showed, that this intervention is functioning with this target group. Participants (families) experienced that they got information, guidance to ordinary life and that the DFG-therapists were listening to them and above all, helping with individual problems and questions. DFG include six meetings and professionals need to attend on a 3-day long education before using this intervention.",[118,31,120],[257,258,259,260],"neurodevelopmental disorders","family health","family functionality","family support","2024-03-13",{"date":263,"type":36},"2024-03-21",{"date":265,"type":36},"2024-01-02",{"date":267,"type":22},"2027-12-31",{"name":269,"class":43},"Tampere University"]