[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"child-health\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:child-health":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,50,78,108,153,184,216,289,320,346],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100633227","maff-crt-reducing-sedentary-behaviour-in-children-100633227",false,"NCT07523945","MAFF-CRT: Reducing Sedentary Behaviour in Children","MAFF-CRT: School-to-Home Trial to Reduce Sedentary Behaviour in Children","MAFF-CRT","Inclusion Criteria:\n\n* Enrolled in participating Portuguese public schools\n* Written informed consent provided by a parent or legal guardian\n* Assent provided by the child\n* Able to participate in light-to-moderate physical activity as part of normal school activities\n\nExclusion Criteria:\n\n* Medical conditions or physical limitations that contraindicate participation in physical activity\n* Cognitive, developmental, or behavioural conditions that would prevent understanding or adherence to the intervention procedures (as assessed by school staff)\n* Lack of parental\u002Flegal guardian consent\n* Concurrent participation in another structured physical activity or behavioural intervention study",true,"ALL",{"count":20,"type":21},200,"ESTIMATED","INTERVENTIONAL",[24],"NA","Children today spend many hours sitting at school and at home, often in front of screens. Prolonged sitting in childhood increases the risk of future health problems such as diabetes, heart disease and poor mental wellbeing. MAFF is a simple school-to-home programme that teaches short, practical movement breaks in the classroom and encourages families to repeat them together at home through structured weekly challenges. Over 12 weeks, we will compare classes using MAFF with classes continuing as usual to assess whether children sit less, move more and improve their wellbeing. If effective, MAFF will provide schools and communities with an easy-to-implement toolkit to promote healthier and more active families.",[27,28,29,30],"Sedentary Behaviors","Physical Inactivity","Child Health","Lifestyle (Sedentary Behavior and Physical Activity)",[32,33,34,35,36],"sedentary behaviour","physical activity","school-based intervention","family-based intervention","randomized controlled trial","NOT_YET_RECRUITING","2026-04-05",{"date":40,"type":41},"2026-04-13","ACTUAL",{"date":43,"type":21},"2026-11-30",{"date":45,"type":21},"2028-12-02",{"name":47,"class":48},"Instituto Politécnico de Setúbal","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":77},"100561662","the-decide-tb-trial-validation-of-treatment-decision-algorithms-for-childhood-tuberculosis-100561662","NCT06593080","The DECIDE-TB Trial; Validation of Treatment Decision Algorithms for Childhood Tuberculosis","Validation of Treatment Decision Algorithms for Childhood Tuberculosis at District Health Care Levels in Mozambique and Zambia - the Decide-TB Cluster-randomized Pragmatic Trial","DTB","Inclusion Criteria:\n\nThe effectiveness assessment will be conducted using aggregated or individual data from direct beneficiaries of the intervention:\n\n* All sick children aged below 15 years entering the selected health facilities (DH and PHC) at either outpatient (OPD) or inpatient (IPD) departments, including children from high-risk groups, as well as children identified as contact of TB cases through community- or facility-based household contact tracing.\n* Children with presumptive TB.\n\nThe WHO definition of presumptive TB will be used, as defined in the 2022 WHO Operational Handbook, namely: children are classified as having presumptive TB if they have unremitting symptoms lasting more than 2 weeks (any one of cough, fever, not eating well or anorexia, weight loss or failure to thrive, fatigue, reduced playfulness or decreased activity) .\n\nThe definitions of presumptive TB have been adapted locally for the programmatic pilot. All children with presumptive TB as defined locally will be considered in the intervention and in secondary effectiveness and sub-group analyses.\n\nHigh-risk group will be defined using the definition in WHO-suggested TDAs A\\&B as children younger than 2 years, CLHIV or children with SAM. CLHIV will be defined per national testing strategy including positive PCR test for children below the age of 18 months. Children will be considered to have SAM (and thereby be eligible for the TB-Speed SAM algorithm) using WHO criteria. These include being \\\u003C5 years with a weight-for-height Z score (WHZ) \\\u003C -3 SDs or mid-upper arm circumference (MUAC) \\\u003C 115 mm (in children over 6 months) or clinical signs of bilateral pitting oedema, and being aged ≥5 years with a body mass index (BMI) for age Z-score \\\u003C -3SD.\n\nExclusion Criteria:\n\nThere will be no exclusion criteria for the programmatic pilot: all children will be offered the intervention.","14 Years",{"count":60,"type":21},30240,[24],"The Decide-TB project aims to generate evidence for the implementation of a comprehensive Treatment Decision Algorithms (TDA) based approach for TB in children living in high TB burden and resource-limited countries, at District Hospital (DH) and Primary Health Centre (PHC) levels, and to facilitate the integration of this evidence within practices and policies.\n\nThis programmatic pilot led by the National TB Programs (NTP) will test a TDA-based approach integrating TB screening, diagnosis, treatment decision-making, and disease severity assessment for shorter treatment eligibility, for use at a lower level of healthcare. This TDA-based approach will be evaluated in a hybrid effectiveness implementation study based on a pragmatic stepped wedge cluster-randomized trial. The Decide TB project will be implemented at the district level, targeting five districts in each country. Each cluster in a district will be made up of one district hospital and six primary health centers. The study will develop a Clinical Decision Support System (CDSS) to operationalize the use of TDAs, and strengthen District Health Information Systems (DHIS2) to collect individual data, which will contribute to monitoring and evaluation, clinical mentoring, and supervision by the country's NTPs.",[64,29,65,66],"Tuberculosis","HIV","Severe Acute Malnutrition","RECRUITING","2026-03-19",{"date":70,"type":41},"2026-03-24",{"date":72,"type":41},"2024-06-01",{"date":74,"type":21},"2027-08-31",{"name":76,"class":48},"Chishala Chabala",29,{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":18,"minAge":85,"maxAge":86,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":93,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":49},"100615193","effect-of-a-mobile-app-for-obese-children-on-eating-attitudes-eating-awareness-and-healthy-eating-self-efficacy-100615193","NCT07289425","Effect of a Mobile App for Obese Children on Eating Attitudes, Eating Awareness, and Healthy Eating Self-Efficacy","The Effect of a Mobile Application Developed for Obese Children on Eating Attitudes, Eating Awareness, and Healthy Eating Self-Efficacy","Inclusion Criteria:\n\n* The child must be between 8 and 10 years old,\n* The child must not have any chronic illnesses other than obesity,\n* The child must be able to read and write in Turkish,\n* The child must be able to use a mobile device,\n* The child must not have a visual impairment,\n* The parent must be willing to participate in the study,\n* The parent must be able to read and write in Turkish,\n* The parent or child must have a smartphone.\n\nExclusion Criteria:\n\n* If they wish to withdraw from the study at any stage of the research,\n* If they do not wish to use the mobile application at any stage of the research.","8 Years","10 Years",{"count":88,"type":21},52,[24],"This study aims to evaluate the effect of a mobile application developed for obese children on eating attitudes, eating awareness, and healthy eating self-efficacy. The application seeks to support children in developing healthy eating habits and to integrate nursing interventions with digital health technologies in combating obesity. Data will be collected through a researcher-developed Information Form and three validated scales: the Eating Attitude Test, the Eating Awareness Scale, and the Healthy Eating Self-Efficacy Scale, completed by both children and parents.",[92,29],"Obesity",[94,95,96,97,98],"Child health","obesity","eating behavior","mindful eating","self efficacy","2026-03-15",{"date":101,"type":41},"2026-03-17",{"date":103,"type":21},"2026-12-15",{"date":105,"type":21},"2027-06-15",{"name":107,"class":48},"Cumhuriyet University",{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":113,"acronym":4,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":18,"minAge":115,"maxAge":4,"enrollmentInfo":116,"targetDuration":4,"studyType":22,"phases":118,"briefSummary":119,"conditions":120,"keywords":134,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":149,"leadSponsor":151,"locationsCount":49},"100613028","integrating-systems-and-basic-income-improving-outcomes-for-families-of-young-children-100613028","NCT07261254","Integrating Systems and Basic Income: Improving Outcomes for Families of Young Children","Advancing Health Equity Via Basic Income + Early Childhood Systems Integration: An RCT of the Baby Bonus Program","Inclusion Criteria:\n\nCaregiver Eligibility Criteria\n\n* 18 and Older\n* Family plans to reside in San Mateo County\n* Does not plan to move from the County in the next year\n* Speaks English and\u002For Spanish\n* Cared for in Postpartum Maternity unit\n\nChild Eligibility Criteria\n\n* Baby is being cared for in well newborn nursery\n* Child is enrolled in Medicaid\n* 36 weeks or older\n* To be discharged home in the custody of the caregiver\n\nExclusion Criteria:\n\nCaregiver Exclusion Criteria\n\n* Will not consent to share data via Epic\u002FStudy\n* Caregiver has significant cognitive impairment\n* Caregiver under contact isolation\n\nChild Exclusion Criteria\n\n* Sibling already enrolled in the Baby Bonus Study\n* Child has significant genetic disorder issues at birth\n* Child is a multiple (not a singleton)","0 Days",{"count":117,"type":21},2400,[24],"Early childhood is a critical period, laying the foundation for future growth and deveopment. This foundational period has an outsized effect, impacting health, well-being and achievement across one's lifespan. The U.S. lacks a cohesive early childhood system to support families with young children ages 0-5. The goal of this randomized controlled trial(RCT) is to test if community-based support via community health workers(CHWs) improves social and health services utilization, and child development. Furthermore, the trial will examine if income support enhances the impact of a CHW integrated system. Participants are English and Spanish speaking families with healthy newborns. This RCT was designed based on family priorities, community capacity and needs in a collective impact model. This trial is anchored at a university based children's hospital and involves many partners: families, county health, county leadership, a leading early childhood non-profit organization, the county's Medicaid managed care organization.",[121,122,123,124,125,126,127,29,128,129,130,131,132,133],"Income","Infant, Newborn","Mothers","Poverty","United States","Healthcare Disparities","Child Care","Community Health Workers","Hispanic or Latino","Medicaid","Child Development","Social Services Utilization","Health Services Utilization",[135,128,130,136,137,138,139,140,141,142,143],"Guaranteed Basic Income","Medi-Cal","Community Partners","Coordinated Care","Coordinated Services","randomized trial","surveys","infant, newborn","newborn nursery","2026-02-10",{"date":146,"type":41},"2026-02-12",{"date":148,"type":41},"2025-04-07",{"date":150,"type":21},"2030-03",{"name":152,"class":48},"Stanford University",{"id":154,"slug":155,"hasResults":11,"nctId":156,"briefTitle":157,"officialTitle":158,"acronym":159,"eligibilityCriteria":160,"healthyVolunteers":17,"sex":18,"minAge":161,"maxAge":58,"enrollmentInfo":162,"targetDuration":4,"studyType":22,"phases":164,"briefSummary":165,"conditions":166,"keywords":170,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":183},"100595081","feasibility-and-efficacy-of-ambulance-based-m-health-for-pediatric-emergencies-feamer-trial-100595081","NCT07027813","Feasibility and Efficacy of Ambulance-Based m-Health for Pediatric Emergencies (FEAMER) Trial","Feasibility and Efficacy of Ambulance-Based m-Health for Pediatric Emergencies in Low Resource Settings (FEAMER) Trial","FEAMER","CHILDREN\n\nInclusion criteria:\n\n* Age 0-14 years\n* Children transported by an SIEHS ambulance with a transport time of ≥20 minutes\n* Children presenting to the ChildLife Emergency Department with a parent\u002F guardian present in the ambulance to consent\n* Children classified as \"Charlie, Delta, Echo\" on the Medical Priority Dispatch System\n\nExclusion Criteria:\n\n• Children transported without an adult parent or guardian\n\nEMERGENCY MEDICAL TECHNICIANS (EMTs)\n\nInclusion Criteria:\n\n• EMTs currently employed by the SIEHS EMS service.\n\nExclusion Criteria:\n\n• EMTs who refuse to participate or consent to the study.\n\nTELEMEDICINE PHYSICIANS (TMPs)\n\nInclusion Criteria:\n\n• TMPs currently employed by the CLF Telemedicine services.\n\nExclusion Criteria:\n\n• TMPs who refuse to participate or consent to the study.","1 Minute",{"count":163,"type":21},900,[24],"Investigators hypothesize that in a low-resource setting, linking ambulances that transport acutely ill children to a remote pediatric emergency physician using a simple audio-video device will improve the quality of these children's medical decisions and health outcomes. For this purpose, the investigators will conduct a study in Karachi, Pakistan, where they will collect medical data for ill children at the time of ambulance pickup, hospital drop-off, and during hospital triage. During transport, one group will receive a telemedicine call from a trained physician, while the other group will receive basic paramedic treatment. The investigators will then compare both groups.",[167,168,29,169],"Emergencies","mHealth","Critical Illness",[171,172,173],"Emergency Medical Services","Ambulance","Telemedicine","2026-01-05",{"date":176,"type":41},"2026-01-07",{"date":178,"type":41},"2025-06-04",{"date":180,"type":21},"2026-09-30",{"name":182,"class":48},"Weill Medical College of Cornell University",3,{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":4,"eligibilityCriteria":190,"healthyVolunteers":11,"sex":18,"minAge":191,"maxAge":192,"enrollmentInfo":193,"targetDuration":195,"studyType":196,"phases":4,"briefSummary":197,"conditions":198,"keywords":202,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":207,"lastUpdatePostDateStruct":208,"startDateStruct":210,"completionDateStruct":212,"leadSponsor":214,"locationsCount":49},"100303339","boston-birth-cohort-study-100303339","NCT03228875","Boston Birth Cohort Study","Early Life Origins of Pediatric and Adult Diseases: Boston Birth Cohort Study","Inclusion Criteria:\n\n* Mothers who deliver singleton live births at Boston Medical Center are eligible for the study.\n\nExclusion Criteria:\n\n* pregnancies that are a result of in vitro fertilization or that involve multiple gestations, fetal chromosomal abnormalities or major birth defects.","0 Years","50 Years",{"count":194,"type":21},24000,"21 Years","OBSERVATIONAL","Early life exposures may lead to adverse effects on health in later life. The Boston birth Cohort study is designed to study a broad array of early life factors and their effects on maternal and child health outcomes.",[199,29,200,201],"Maternal Health","Pregnancy Complications","Birth Outcome, Adverse",[203,204,205,206],"Boston Birth Cohort","Early life origins of pediatric and adult disease","Gene environment interaction","Health across life course and generations","2025-09-11",{"date":209,"type":41},"2025-09-17",{"date":211,"type":41},"1998-10",{"date":213,"type":21},"2028-12",{"name":215,"class":48},"Johns Hopkins Bloomberg School of Public Health",{"id":217,"slug":218,"hasResults":11,"nctId":219,"briefTitle":220,"officialTitle":221,"acronym":222,"eligibilityCriteria":223,"healthyVolunteers":17,"sex":18,"minAge":224,"maxAge":4,"enrollmentInfo":225,"targetDuration":4,"studyType":196,"phases":4,"briefSummary":227,"conditions":228,"keywords":251,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":280,"lastUpdatePostDateStruct":281,"startDateStruct":283,"completionDateStruct":285,"leadSponsor":287,"locationsCount":49},"100469557","generation-victoria-cohort-2020s-a-statewide-longitudinal-cohort-study-of-victorian-children-and-their-parents-100469557","NCT05394363","Generation Victoria Cohort 2020s: A Statewide Longitudinal Cohort Study of Victorian Children and Their Parents","Generation Victoria Cohort 2020s. A Statewide Longitudinal Cohort of Victorian Children and Their Parents","GenV","Inclusion Criteria (Children):\n\n* Birth date between 4th October 2021 and 3rd October 2023\n* Live at the time of recruitment\n* Residing in Victoria at the time of recruitment\n* Has a legally acceptable representative capable of understanding the informed consent document and providing consent on the child's behalf, who provides a signed and dated informed consent form (e.g. a parent\u002Fguardian)\n\nInclusion Criteria (Adults):\n\n* Be a parent or guardian of a child who meets the eligibility criteria above\n* Provide a signed and dated informed consent form or have a legally acceptable representative capable of understanding the informed consent document and providing consent on the participant's behalf.\n\nExclusion criteria:\n\n* Children who are deceased at the time of recruitment (i.e. still born or died after birth) and their parents\u002Fguardians\n* Families unable to provide informed consent in any of the languages available","1 Day",{"count":226,"type":21},150000,"Generation Victoria (GenV) is a longitudinal, population-based study of Victorian children and their parents that will bring together data on a wide range of conditions ,exposures and outcomes. GenV blends study-collected, study-enhanced and linked data. It will be multi-purpose, supporting observational, interventional, health services and policy research within the same cohort. It is designed to address physical, mental and social issues experienced during childhood, as well as the antecedents of a wide range of diseases of ageing. It seeks to generate translatable evidence (prediction, prevention, treatments, services) to improve future wellbeing and reduce the future disease burden of children and adults.\n\nThe GenV Cohort 2020s is open to all children born over a two-year period, and their parents, residing in the state of Victoria Australia. The GenV Cohort 2020s is preceded by an Advance Cohort of children born between 5 Dec 2020 and 3 October 2021, and their parents. This comprises all families recruited at GenV's Vanguard hospital (Joan Kirner Women's and Children's) and at birthing hospitals throughout Victoria as GenV scaled up to commence recruiting for the GenV Cohort 2020s. The Advance Cohort have ongoing and full participation in GenV for their lifetime unless they withdraw but may have less complete data and biosamples.",[229,230,231,29,232,233,234,235,236,237,238,239,240,131,241,242,243,244,245,246,247,92,248,249,250],"Mental Health","Child Wellbeing","Infant Health","Reproductive Health","Healthy Aging","Health Equity","Quality of Life","Social Determinants of Health","Environmental Exposure","Genetics","Cognition","Learning","Congenital Abnormalities","Disability","Injuries","Communicable Diseases","Noncommunicable Diseases","Physical Fitness","Diet","Allergy and Immunology","Inflammation","Intergenerational Relations",[252,222,253,254,255,29,256,257,258,259,260,123,261,262,263,264,265,266,267,268,269,270,234,271,272,273,274,275,276,277,236,278,279],"Generation Victoria","Cohort Studies","Data Collection","Data Linkage","Midlife Health","Children","Infants","Family","Parents","Fathers","Life course perspective","Population Health","Longitudinal Studies","Genetics, population","Demography","Epidemiology","Health Disparity","Minority Health","Vulnerable Populations","Clinical Trial","Randomized Controlled Trial","Pragmatic Clinical Trial","Health Services Research","Economic Models","Value of Life","Geographic Information Systems","Climate Change","Built Environment","2025-07-30",{"date":282,"type":41},"2025-08-03",{"date":284,"type":41},"2021-10-04",{"date":286,"type":21},"2033-10",{"name":288,"class":48},"Murdoch Childrens Research Institute",{"id":290,"slug":291,"hasResults":11,"nctId":292,"briefTitle":293,"officialTitle":293,"acronym":294,"eligibilityCriteria":295,"healthyVolunteers":11,"sex":296,"minAge":297,"maxAge":298,"enrollmentInfo":299,"targetDuration":4,"studyType":22,"phases":301,"briefSummary":302,"conditions":303,"keywords":305,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":311,"lastUpdatePostDateStruct":312,"startDateStruct":314,"completionDateStruct":316,"leadSponsor":318,"locationsCount":4},"100592236","clinical-and-cost-effectiveness-of-learning-through-play-plus-culturally-adapted-cognitive-behaviour-therapy-for-postnatal-depression-in-nigeria-100592236","NCT06990802","Clinical and Cost-effectiveness of Learning Through Play Plus Culturally Adapted Cognitive Behaviour Therapy for Postnatal Depression in Nigeria","LTP+CaCBT","Inclusion Criteria:\n\n* 18 years and above\n* A mother with a child (0-3 years)\n* Able to provide full consent for their participation\n* A resident of the trial catchment areas\n* Able to complete a baseline assessment\n* Score 5 or above on Patient Health Questionnaire (PHQ-9)\n* available for follow-up at 4 and 6 months post-enrolment\n\nExclusion Criteria:\n\n* Less than 18 years\n* Medical disorder that would prevent participation in a clinical trial, such as Tuberculosis or heart failure\n* Temporary residents are unlikely to be available for follow-up\n* Active suicidal ideation or any other severe mental disorder\n* Patients currently undergoing severe mental health treatment\n* Non-residents of the trial environs\n* Unable to consent\n* Unable to speak and understand English language\n* Other significant physical or learning disability","FEMALE","18 Years","49 Years",{"count":300,"type":21},432,[24],"Background: We aim to examine the effectiveness of Learning Through Play and Cognitive Behaviour Therapy (LTP+CaCBT), a culturally appropriate psychosocial intervention to address postnatal depression among Nigerian women and improve the well-being of their children. Women of reproductive age (ages 16 to 49) comprise about 60 million of Nigeria's 230 million people. About 30% of these mothers experience postnatal depression. The global health challenge our research addresses is that one in three women worldwide experience postnatal depression and suicidal thoughts after childbirth, with long-term negative consequences on their children and families. Since 30% of Nigerian mothers suffer from postnatal depression, they have significant risks of transferring intergenerational mental health problems to their children. Over 250 million children are at risk of lacking developmental support in low- or middle-income countries, including Nigeria, due to postnatal depression, and this limits the children from reaching their full potential in life. The treatment gap for postnatal depression in Nigeria is huge due to a shortage of mental health specialists. Culturally appropriate, nonspecialist-delivered interventions are very limited in Nigeria. Our proposal aims to address this gap in treating postnatal depression using non-specialists called Indigenous Community Health Workers (CHWs), who are more culturally knowledgeable, as the World Health Organisation recommended in their task-shifting strategy.\n\nMethods: We will evaluate the treatment, costs and implementation outcomes of LTP+CaCBT with 432 depressed mothers. Eligible participants (mother-child pairs) will be randomly selected to receive LTP+CaCBT and Treatment As Usual (TAU) or TAU alone. Our LTP+CaCBT intervention is a manualised 12-session (90-minute each) of mother-child play activities delivered in-person by CHWs under the supervision of clinical psychologists\u002Fpsychiatrists. The eligible mothers (aged 16-49 years who have children between ages 0-36 months) will be assessed for depression before the intervention and then again at 4 months and 6 months afterwards. We will conduct interviews and focus group discussions to understand participants' and CHWs' experiences of the intervention",[304,29],"Postnatal Depression",[306,94,307,308,309,310],"Postnatal depression","Intervention","Parenting","Childbirth","Maternal mental health","2025-05-17",{"date":313,"type":41},"2025-05-25",{"date":315,"type":21},"2026-07",{"date":317,"type":21},"2028-07",{"name":319,"class":48},"Nottingham Trent University",{"id":321,"slug":322,"hasResults":11,"nctId":323,"briefTitle":324,"officialTitle":325,"acronym":4,"eligibilityCriteria":326,"healthyVolunteers":17,"sex":18,"minAge":327,"maxAge":85,"enrollmentInfo":328,"targetDuration":4,"studyType":22,"phases":330,"briefSummary":331,"conditions":332,"keywords":335,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":338,"lastUpdatePostDateStruct":339,"startDateStruct":341,"completionDateStruct":342,"leadSponsor":344,"locationsCount":49},"100589448","outcomes-of-a-game-based-educational-intervention-healthy-kids-100589448","NCT06954545","Outcomes of a Game-based Educational Intervention: Healthy Kids","Effectiveness of a Role-play Based School Intervention in Primary School Students: a Non-randomized Cluster Controlled Trial","Inclusion Criteria:\n\n* All participants who do not meet the criteria of whether or not they agree to participate in the study will be included in the study.\n\nExclusion Criteria:\n\n* neurodevelopmental delays\n* metabolic disorders potentially leading to obesity\n* physical disabilities\n* those whose parents or guardians declined participation.","6 Years",{"count":329,"type":21},400,[24],"235 \u002F 5.000 Investigators aimed to reduce the risk of obesity by trying a new intervention method that is role-play based, interactive and fun with age-appropriate play materials, considering that learning through play is more efficient.",[333,29,334],"Obesity and Overweight","Physical Activity",[336,337],"educational intervention","prevention of obesity","2025-04-24",{"date":340,"type":41},"2025-05-01",{"date":340,"type":21},{"date":343,"type":21},"2025-08-01",{"name":345,"class":48},"Marmara University",{"id":347,"slug":348,"hasResults":11,"nctId":349,"briefTitle":350,"officialTitle":350,"acronym":351,"eligibilityCriteria":352,"healthyVolunteers":17,"sex":18,"minAge":353,"maxAge":354,"enrollmentInfo":355,"targetDuration":4,"studyType":22,"phases":357,"briefSummary":358,"conditions":359,"keywords":366,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":371,"lastUpdatePostDateStruct":372,"startDateStruct":374,"completionDateStruct":376,"leadSponsor":378,"locationsCount":49},"100576898","improvements-in-daily-activity-and-exercise-in-school-children-the-actchild-study-100576898","NCT06791278","Improvements in Daily Activity and Exercise in School Children: the ActChild Study","ActChild","Inclusion Criteria:\n\n* Schoolchildren, 0.-1. Grade, 5-8 years of age,\n* Resident in Aarhus Municipality\n\nExclusion Criteria:\n\n\\- None","5 Years","12 Years",{"count":356,"type":21},600,[24],"The goal of this clinical trial is to assess the health-related effects of an exercise intervention in children aged 5-8 years.\n\nMain research questions:\n\n* Does a municipality-driven exercise intervention improve physical activity levels in children?\n* Does a municipality-driven exercise intervention improve sleep parameters in children?\n* Does a municipality-driven exercise intervention improve eating behaviors in children?\n* Does a municipality-driven exercise intervention improve quality of life in children?\n\nStudy Design:\n\nParticipants will be assigned to either:\n\n* Intervention group: Attend 1-2 weekly sessions of 45-60 minutes of child-friendly exercise for 1 year.\n* Control group: Receive no intervention.\n\nData Collection:\n\nParticipants will:\n\n* Complete questionnaires at baseline, and at 1-year, 3-year, and 5-year follow-ups.\n* Wear accelerometers for 7 consecutive days at baseline, and at 1-year, 3-year, and 5-year follow-ups.",[360,257,361,29,362,334,363,364,365],"Healthy Children","Children in School","Child Behavior","Sleep","Eating Behaviors","Child Obesity",[367,257,368,369,370,363,334,235],"Exercise Intervention","School Children","CEBQ","Eating Behavior","2025-01-22",{"date":373,"type":41},"2025-01-24",{"date":375,"type":21},"2025-02-04",{"date":377,"type":21},"2032-12",{"name":379,"class":48},"University of Aarhus"]