[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"social-functioning\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:social-functioning":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,42,73,107,137,164,192,211],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100633466","emerging-technologies-and-teen-mental-health-100633466",false,"NCT07527052","Emerging Technologies and Teen Mental Health","Inclusion Criteria:\n\n* Adolescents must (A) be between ages 12 and 17 years\n* (B) have a positive screen for suicide risk (i.e. endorsement of suicidal ideation via self-report or parent-report)\n* (C) have access to a personal social media account\n* (D) be fluent in English\n* (E) have available a parent who is fluent in English or Spanish.\n\nExclusion Criteria:\n\n* Adolescents must not (A) have cognitive impairment or developmental delay which does not allow for the completion of basic study procedures (i.e., reading and filling out questionnaires; talking to a clinician)\n* (B) show imminent risk or a history of hurting themselves or others requiring intensive and restrictive services.","ALL","12 Years","17 Years",{"count":19,"type":20},200,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study will recruit teens who are experiencing subacute suicidal ideation to test the effect of a brief psychoeducational intervention focused on social media use wherein youth learn about active and prosocial use of social media platforms.",[26,27,28],"Social Functioning","Emotional Distress","Suicidal Ideation","RECRUITING","2026-04-08",{"date":32,"type":33},"2026-04-14","ACTUAL",{"date":35,"type":33},"2026-03-20",{"date":37,"type":20},"2028-12",{"name":39,"class":40},"Florida International University","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":15,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":72},"100546486","internet-based-interventions-for-cardiac-arrest-survivors-100546486","NCT06395558","intErnet-based iNterventions FOR Cardiac arrEst suRvivors","Internet-Based Interventions for Cardiac Arrest Survivors","ENFORCER","Inclusion Criteria:\n\n* Hospital discharge after out-of-hospital cardiac arrest with Cerebral Performance Category 1 or 2\n* Informed consent for participation in the study\n* Native Italian speaker or adequate understanding of the Italian language\n* Adequate ability to use the web to guarantee access to the contents\n\nExclusion Criteria:\n\n* Previous cognitive dysfunction\n* Previous psychiatric disease\n* Previous episode of out-of-hospital cardiac arrest","18 Years","80 Years",{"count":53,"type":20},106,[23],"This randomized clinical trial will test whether an internet-based lifestyle intervention administered through a web app can foster Health Related Quality of Life in patients who survived an out-of-hospital cardiac arrest and suffer from these symptoms",[57,58,59,60,26,61],"Cognitive Impairment","Depression, Anxiety","Cardiac Arrest","Quality of Life","Sexual Dysfunction","2026-03-25",{"date":64,"type":33},"2026-03-30",{"date":66,"type":33},"2024-08-05",{"date":68,"type":20},"2027-10-01",{"name":70,"class":71},"Azienda Usl di Bologna","OTHER_GOV",2,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":80,"sex":15,"minAge":81,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":21,"phases":84,"briefSummary":85,"conditions":86,"keywords":92,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":41},"100629466","project-hopeful-a-pn-rct-with-implementation-science-100629466","NCT07475039","Project HOPEFUL: A PN-RCT With Implementation Science","Project HOPEFUL (Helping Older PErsons Find Useful Links): Replicating a Partially Nested Randomized Control Trial With Implementation Science","In order to be eligible as a participant in this study, an individual must meet all of the following criteria:\n\n1. Provision of verbal informed consent\n2. Classify as an Older Adult (65+)\n3. Stated willingness and ability to comply with all study procedures\n4. Receive home and community-based services (HCBS) through the Aging Services Network (i.e. HDM (home delivered meals services), CM (congregate meals), etc.)\n5. Be affiliated with the triple As and aging entities we have partnered with\n\nIn order to be eligible to be a trained provider in this study, an individual must meet all of the following criteria:\n\n1. Provision of written informed consent\n2. State willingness to comply with all study procedures\n3. Be a staff or volunteer within the ASN (Aging Services Network), specifically within the triple As and aging entities we have partnered with\n4. Meet Wymann and colleagues (2008) criteria for being a \"natural helpers\"42 (i.e. be warm, empathic, and having ongoing interaction with participants through one's job role)\n5. Be recommended by the aging entity leadership as meeting these qualifications\n\nIn order to be eligible to be a leadership personnel in this study, an individual must meet all of the following criteria:\n\n1. Provision of written informed consent\n2. State willingness to comply with all study procedures\n3. Be a in a leadership position within the aging entity or triple A in which we partnered, and have worked with the study team in helping implement the 8 week program\n\nExclusion criteria for Participants:\n\n1. Had a dementia diagnosis, or another form of cognitive impairment, and\u002For hearing impairment that would preclude phone conversation.\n2. Participation in another warm calling behavioral treatment or intervention study simultaneously occurring\n\nExclusion criteria for trained natural helpers:\n\n1. Does not have ongoing interactions with potential old adult participants (i.e. is a part of an optimized nutrition service provider in which they do not serve the same older adults consistently over time)\n2. Participation in another warm calling behavioral treatment or intervention study simultaneously occurring\n\nExclusion criteria for aging leaders:\n\n1. Has not worked with the study team directly in implementing the 8-week treatment\n2. Is not familiar with the implementation of the program",true,"55 Years",{"count":83,"type":20},400,[23],"This PN-RCT replicates and evaluates an 8-week warm calling treatment (i.e. caring contacts) delivered to older adults receiving home and community-based services (HCBS; classified as \"homebound\") in 20-30 minute call \"dosages\", across 3 conditions, while adding in implementation science measures at multiple levels. Conditions include 2 treatment (i.e. treatment provided by helpers trained in a standardized and manualized Belongingness and Empathy training grounded in narrative reminiscence and the befriending literature (BE condition), and treatment provided by helpers trained in BE + a standardized, manualized, and evidence based suicide intervention training, the Aging Variant of LivingWorks ASIST (BE + ASIST condition), and 1 control (no treatment during the trial; opportunity to receive treatment after the 8 weeks). At the conclusion of treatment, acceptability, appropriateness, feasibility, useability, and sustainability of the program will be evaluated by interventionists, senior center leadership, and regional leadership.",[87,88,89,26,60,90,91],"Older Adults (50-90 Years)","Mental Health","Depression and Suicide Ideation","Thwarted Belongingness","Perceived Burdensomeness",[93,94,95,96,97],"Older adults","Intervention trial","Suicidality","Home Bound Meals","warm-calling","2026-03-11",{"date":100,"type":33},"2026-03-16",{"date":102,"type":33},"2025-09-05",{"date":104,"type":20},"2030-08-30",{"name":106,"class":40},"University of Florida",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":80,"sex":15,"minAge":114,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":118,"phases":4,"briefSummary":119,"conditions":120,"keywords":124,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":41},"100625299","psychological-correlates-of-developmental-delays-in-preschool-children-100625299","NCT07420829","Psychological Correlates of Developmental Delays in Preschool Children","Perinatal, Cognitive, Linguistic, and Social-emotional Correlates of Developmental Delay in Polish Preschool Children From a Biopsychosocial Perspective","Inclusion Criteria:\n\n* Children aged 3 to 6 years at the time of assessment.\n* Attendance at preschool education.\n* Written informed consent provided by a parent or legal guardian.\n* Ability to participate in standardized psychological assessment.\n* Assignment to one of the predefined study cohorts based on developmental history and clinical information.\n\nExclusion Criteria:\n\n* Age below 3 years or above 6 years.\n* Severe acute medical condition preventing participation.\n* Severe uncorrected sensory impairment interfering with valid assessment.\n* Lack of parental informed consent.","3 Years","6 Years",{"count":117,"type":20},500,"OBSERVATIONAL","The goal of this observational study is to investigate perinatal, cognitive, linguistic and social-emotional correlates of developmental delays of preschool children.\n\nThe study group consist of minimal 500 children between 3 and 6 years of age who will be examined by qualified diagnosticians. Participants will be evaluated with tasks related to the studied variables: cognitive functioning, linguistic skills and social-emotional functioning. Furthermore informations regarding social-emotional functioning of children, will be collected from parents.\n\nThe main questions it aims to answer are:\n\n1. Is there a relationship between perinatal factors and risk of occurrence of developmental delay disorder?\n2. Is there a specific pattern of cognitive functioning in preschool children with indicated developmental delay disorder?\n3. Is there a specific pattern of social-emotional functioning in preschool children with indicated developmental delay disorder?\n4. Do gender and age moderates specific patterns of cognitive and socialemotional functioning in the studied groups?\n\nResearchers will compare the following groups of children between 3 and 6 years old:\n\n1. With perinatal risks factors\n2. With developmental delay disorder:\n\n   1. children with early intervention\n   2. children with delayed speech development\n3. Control group",[121,122,26,123],"Development Delay","Child Development","Speech Delay",[125,126,127],"early intervention","development","language","2026-02-11",{"date":130,"type":33},"2026-02-19",{"date":132,"type":33},"2025-09-01",{"date":134,"type":20},"2027-01",{"name":136,"class":71},"Bartosz M. Radtke",{"id":138,"slug":139,"hasResults":11,"nctId":140,"briefTitle":141,"officialTitle":142,"acronym":4,"eligibilityCriteria":143,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":81,"enrollmentInfo":144,"targetDuration":4,"studyType":21,"phases":146,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":155,"lastUpdatePostDateStruct":156,"startDateStruct":158,"completionDateStruct":160,"leadSponsor":162,"locationsCount":41},"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).",{"count":145,"type":20},74,[23],"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.",[149,150,151,152,26,153,154],"Depression","Anxiety","PTSD","Family Dynamics","Family Support","Family Relations","2025-09-25",{"date":157,"type":33},"2025-10-01",{"date":159,"type":33},"2024-05-31",{"date":161,"type":20},"2026-08-30",{"name":163,"class":40},"University of Illinois at Chicago",{"id":165,"slug":166,"hasResults":11,"nctId":167,"briefTitle":168,"officialTitle":169,"acronym":4,"eligibilityCriteria":170,"healthyVolunteers":80,"sex":15,"minAge":171,"maxAge":172,"enrollmentInfo":173,"targetDuration":4,"studyType":118,"phases":4,"briefSummary":175,"conditions":176,"keywords":180,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":183,"lastUpdatePostDateStruct":184,"startDateStruct":186,"completionDateStruct":188,"leadSponsor":190,"locationsCount":41},"100524105","characteristics-of-injury-claims-by-chronic-pain-patients-100524105","NCT06104384","Characteristics of Injury Claims by Chronic Pain Patients","Socio-demographics of Injury Insurance Claims by Chronic Pain Patients","Inclusion Criteria:\n\n* adult chronic pain patients\n* patients with injury claim\n\nExclusion Criteria:\n\n* pediatric patients\n* patients without injury claim","20 Years","99 Years",{"count":174,"type":20},1000,"Chronic pain is associated with injuries and disabilities. This prospective observational study explores the injury or disability claims made by chronic pain patients. It evaluates the socio-demographics of the patient population. It explores the impact of pain clinic services on the patients' injury rehabilitation, insurance claim outcome, and socioeconomic situation.",[26,177,178,179],"Chronic Pain","Injuries","Disabilities Multiple",[181,182],"Injury Claim","Disability Claim","2025-01-23",{"date":185,"type":33},"2025-01-27",{"date":187,"type":33},"2018-01-02",{"date":189,"type":20},"2025-12-31",{"name":191,"class":40},"Salem Anaesthesia Pain Clinic",{"id":193,"slug":194,"hasResults":11,"nctId":195,"briefTitle":196,"officialTitle":197,"acronym":4,"eligibilityCriteria":198,"healthyVolunteers":80,"sex":15,"minAge":171,"maxAge":172,"enrollmentInfo":199,"targetDuration":4,"studyType":118,"phases":4,"briefSummary":200,"conditions":201,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":183,"lastUpdatePostDateStruct":206,"startDateStruct":207,"completionDateStruct":209,"leadSponsor":210,"locationsCount":41},"100521970","pain-clinic-provides-public-health-safety-100521970","NCT06076512","Pain Clinic Provides Public Health Safety","Pain Clinic Provides Public Health and Safety Services","Inclusion Criteria:\n\n* adult chronic pain patients\n* patients with psychosocial problems\n\nExclusion Criteria:\n\n* pediatric patients\n* patients with severe cognitive dysfunction",{"count":174,"type":20},"Chronic pain is associated with psychological disorders; which may affect a patient's socioeconomic, legal, domestic, and employment situations. This prospective observational study evaluates the impact of pain management on patients' health, social, economic, and employment status. It explores the impact of pain clinic services on patients' mental health, family health, public health, road safety, addiction situation, public safety, injury rehabilitation and employment situation.",[26,202,203,204,205,177],"Addiction, Substance","Safety Issues","Road Injury","Patient Compliance",{"date":185,"type":33},{"date":208,"type":33},"2018-02-02",{"date":189,"type":20},{"name":191,"class":40},{"id":212,"slug":213,"hasResults":11,"nctId":214,"briefTitle":215,"officialTitle":216,"acronym":4,"eligibilityCriteria":217,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":218,"enrollmentInfo":219,"targetDuration":4,"studyType":21,"phases":221,"briefSummary":222,"conditions":223,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":228,"startDateStruct":230,"completionDateStruct":232,"leadSponsor":234,"locationsCount":41},"100534756","the-prism-social-needs-prism-sn-intervention-for-adolescents-and-young-adults-with-cancer-100534756","NCT06242964","The PRISM-Social Needs (PRISM-SN) Intervention for Adolescents and Young Adults With Cancer","The Promoting Resilience in Stress Management-Social Needs (PRISM-SN) Intervention for Adolescents and Young Adults With Cancer: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 12-25 years\n* Diagnosed with new malignancy treated with chemotherapy and\u002For radiation \\\u003C6-months\n* Able to speak in the English language\n* Able to read in the English language\n* Cognitively able to participate in intervention sessions and complete surveys\n\nExclusion Criteria:\n\n* Aged \\\u003C12 or \\>25 years\n* Diagnosed with recurrent malignancy\n* Diagnosed with new malignancy \\>6 months\n* Not receiving chemotherapy and\u002For radiation\n* Not able to speak in the English language\n* Not able to read in the English language\n* Not cognitively able to participate in intervention session or complete surveys","25 Years",{"count":220,"type":20},100,[23],"The goal of this study is to establish feasibility, acceptability, and proof-of-concept of an psychosocial intervention adapted to address social health needs of adolescents and young adults (AYAs) newly diagnosed with cancer. The aims of this study are to:\n\n1. Determine if the Promoting Resilience in Stress Management - Social Needs (PRISM-SN) adapted intervention is feasible and acceptable, defined via program uptake and retention and patient-reported feedback.\n2. Explore whether PRISM-SN improves social outcomes at 12-week follow-up compared to usual care.\n\nParticipants will be randomized to receive usual psychosocial care or the PRISM-SN program. Participants on both arms will complete patient-reported outcome surveys at enrollment and 12-weeks later. Researchers will compare participants who received the PRISM-SN program to those who received usual care to see if the program improves psychosocial outcomes.",[224,26,225,226],"Cancer","Psychosocial Functioning","Coping Skills","2024-06-23",{"date":229,"type":33},"2024-06-25",{"date":231,"type":33},"2024-05-15",{"date":233,"type":20},"2026-07-31",{"name":235,"class":40},"Seattle Children's Hospital"]