[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"preventive-health-services\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:preventive-health-services":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,79,114,138,171,204],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":43,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":78},"100643981","health-ahead-comparative-effectiveness-study-100643981",false,"NCT07669168","Health Ahead Comparative Effectiveness Study","Health Ahead: Sequential Comparative-Effectiveness Studies Toward Automated, Universally Deployable Preventive Health Screening","HACE","Inclusion Criteria:\n\n* Age 18 years or older\n* Willing and able to provide written informed consent, or enrollment with consent of a legally authorized representative\n* Willing to participate in longitudinal follow-up.\n\nExclusion Criteria:\n\n\\- Age under 18 years.",true,"ALL","18 Years",{"count":21,"type":22},1000000,"ESTIMATED","INTERVENTIONAL",[25],"NA","The Health Ahead Comparative Effectiveness Study is a pragmatic, parallel-arm interventional platform that systematically compares successive changes to preventive health screening - each isolated as a single variable against current practice - on the path toward a fully automated screening system deployable in any environment, including the most isolated and resource-limited communities. Each comparison is evaluated with a common set of engagement, behavior-change, experience, cost, and longitudinal outcome measures, allowing results to accumulate on a consistent yardstick across the life of the platform.\n\nThe first comparison evaluates static versus interactive personalized health report delivery. Subsequent pre-planned comparisons, added by protocol amendment, evaluate mobile community versus fixed laboratory screening; and a hybrid medical-droid plus human-delivery model versus human-only screening. All participants are simultaneously enrolled in the 100-Year Human Aging Study and the Human Observatory Study, contributing individual longitudinal and population-level causal inference data through those protocols.",[28,29,30,31,32,33,34,35,36,37,38,39,40,41,42],"Health Services Accessibility","Rural Health","Medically Underserved Area","Preventive Health Services","Patient Participation","Health Behavior","Aging","Cardiovascular Diseases","Metabolic Syndrome","Cognitive Dysfunction","Frailty","Activities of Daily Living","Health Related Quality of Life","Health Equity","Telemedecine",[44,45,46,47,48,41,29,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65],"Sequential Platform Trial","Interactive Health Report","Health Activation","Mobile Health Screening","Comparative Effectiveness","Medically Underserved","Preventive Medicine","Patient Engagement","Cardiopulmonary Exercise Testing","Body Composition","DEXA","Health Ahead Bus","Mobile Clinic","Automated Screening","Medical Droids","Biological Age","Healthspan","Longevity","Life Expectancy","Chronic Disease","Cost-Effectiveness","Health Services Research","RECRUITING","2026-06-20",{"date":69,"type":70},"2026-06-25","ACTUAL",{"date":72,"type":22},"2026-06-09",{"date":74,"type":22},"2099-12-31",{"name":76,"class":77},"William Brandenburg, MD","INDUSTRY",1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":17,"sex":87,"minAge":19,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":23,"phases":91,"briefSummary":92,"conditions":93,"keywords":96,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":4},"100633013","effect-of-health-belief-model-based-education-on-cervical-cancer-knowledge-and-hpv-vaccine-attitudes-in-women-100633013","NCT07521163","Effect of Health Belief Model-Based Education on Cervical Cancer Knowledge and HPV Vaccine Attitudes in Women","The Effect of a Health Belief Model-Based Educational Intervention on Women's Knowledge of Cervical Cancer and Their Attitudes and Beliefs Toward HPV Vaccination: A Randomized Controlled Study","HBM-HPV","Inclusion Criteria:\n\n* Women aged 18-49 years\n* Attending the Tusba Training Family Health Center\n* Able to read and write Turkish\n* Willing to participate in the study\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Having received HPV vaccination previously\n* History of cervical cancer\n* Presence of severe psychiatric, cognitive, or communication disorders\n* Inability to attend the educational sessions","FEMALE","49 Years",{"count":90,"type":22},100,[25],"This study aims to evaluate the effect of a Health Belief Model-based educational intervention on women's knowledge of cervical cancer and their attitudes and beliefs toward HPV vaccination. The study will be conducted among women aged 18-49 years attending a primary health care center in Van, Turkey. Participants will be assigned to intervention and control groups. The intervention group will receive a structured, face-to-face educational program, while the control group will receive routine care. Data will be collected using validated questionnaires before and after the intervention. The findings are expected to contribute to improving preventive health behaviors and increasing HPV vaccination awareness among women.",[94,95,31],"Cervical Cancer","Human Papillomavirus Infection",[97,98,99,100,101,102],"Health Belief Model","HPV Vaccination","Cervical Cancer Screening","Health Education","Primary Health Care","Women's Health","NOT_YET_RECRUITING","2026-04-09",{"date":106,"type":70},"2026-04-15",{"date":108,"type":22},"2026-04-20",{"date":110,"type":22},"2026-06-30",{"name":112,"class":113},"Muhammet Faruk Yigit","OTHER",{"id":115,"slug":116,"hasResults":11,"nctId":117,"briefTitle":118,"officialTitle":119,"acronym":4,"eligibilityCriteria":120,"healthyVolunteers":11,"sex":18,"minAge":121,"maxAge":122,"enrollmentInfo":123,"targetDuration":4,"studyType":23,"phases":125,"briefSummary":126,"conditions":127,"keywords":4,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":78},"100624859","improving-ldl-c-levels-through-temporal-self-regulation-theory-based-personality-tailored-health-messages-100624859","NCT07415109","Improving LDL-C Levels Through Temporal Self-regulation Theory-based, Personality-tailored Health Messages","Improving LDL-C Levels Through Temporal Self-regulation Theory-based, Personality-tailored Health Messages: A Three-Arm Randomized Controlled Trial","Inclusion Criteria:\n\n* New participants of RESET who have given consent to be contacted for future studies\n* ≥21 years old\n\nExclusion Criteria:\n\n* are not able to read, write or communicate in English","21 Years","65 Years",{"count":124,"type":22},3000,[25],"The study is meant to run parallel to the larger study, RESET. The goal of this study is to to evaluate the effectiveness of a once-off general and personality-tailored text message on GP consultation among RESET participants identified to have high LDL-C. The main question it aims to answer is:\n\nWill participants exposed to personality tailored advice have a higher adherence to GP consultation compared to the participants in the control group?\n\nResearchers will compare a personalized message to a general message (with no personalization according to patients personality type) and control group to see if the messages increase adherence.\n\nParticipants are required to complete two questionnaires: one before and one after they receive their RESET results.",[128,31],"Adherence","2026-04-07",{"date":131,"type":70},"2026-04-13",{"date":133,"type":70},"2025-11-25",{"date":135,"type":22},"2028-11",{"name":137,"class":113},"National University Health System, Singapore",{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":143,"acronym":4,"eligibilityCriteria":144,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":122,"enrollmentInfo":145,"targetDuration":4,"studyType":23,"phases":147,"briefSummary":148,"conditions":149,"keywords":157,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":167,"leadSponsor":169,"locationsCount":78},"100570815","mhe3-clinical-trial---overcoming-obstacles-100570815","NCT06712147","MHE3 Clinical Trial - Overcoming Obstacles","A Promotora-centric Community Collaborative to Improve Connections to Mental Health Service","Inclusion criteria:\n\n* Has heritage or self-identifies as Hispanic and\u002For Latino\u002Fa\n* Must speak English or Spanish\n* Primary residence is in 95116, 95122, 95127, 95112, 95111, 95121,95148, or 95133 zip codes\n\nExclusion criteria:\n\n* Persons from the same household\n* First degree family member",{"count":146,"type":22},192,[25],"The goal of this clinical trial is to increase and strengthen connections between Latino\u002Fa individuals and mental health services. Through this intervention, the investigators aim to improve mental health literacy, decrease stigma, increase coping skills, and increase mental health help seeking, even before they are in crisis. Participants will be asked to participate in six educational sessions hosted by Promotores de Salud.",[150,151,152,31,153,154,155,156],"Mental Health Services","Community Mental Health Services","Community Health Services","Counseling","Community Networks","Community Participation","Hispanic or Latino",[158,159,160,161],"mental health","promotores de salud","help-seeking","community resources","2026-03-31",{"date":164,"type":70},"2026-04-06",{"date":166,"type":70},"2025-01-06",{"date":168,"type":22},"2026-11",{"name":170,"class":113},"Stanford University",{"id":172,"slug":173,"hasResults":11,"nctId":174,"briefTitle":175,"officialTitle":176,"acronym":4,"eligibilityCriteria":177,"healthyVolunteers":11,"sex":18,"minAge":178,"maxAge":179,"enrollmentInfo":180,"targetDuration":4,"studyType":23,"phases":182,"briefSummary":183,"conditions":184,"keywords":189,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":195,"lastUpdatePostDateStruct":196,"startDateStruct":198,"completionDateStruct":200,"leadSponsor":202,"locationsCount":78},"100540097","the-via-family-20---a-family-based-intervention-for-families-with-parental-mental-illness-100540097","NCT06312410","The VIA Family 2.0 - a Family Based Intervention for Families with Parental Mental Illness","The VIA Family 2.0 Study: a Randomized Clinical Trial Evaluating Family-based Interventions for Children Born to Parents with Mental Disorders","Inclusion Criteria:\n\n* At least one of the parents must be living in Capital Region or in Region North, Denmark, and at least one biological child under age 18 must be living with one of the parents. Only biological children of the parent with at mental health problem can be included.\n* The parent with the mental health problems has at some point been diagnosed in the secondary sector and has within the last three years been treated in the primary sector (GP or private psychiatric clinic) or in the secondary sector (hospital psychiatry).\n* Patients with substance abuse can only be included if substance abuse is a secondary diagnosis to another mental illness disorder being treated within the secondary sector during the last three years.\n* All adult participants must give informed consent. Both parents will need to consent in case of shared custody, but do not have to participate if they are reluctant to do so.\n\nExclusion Criteria:\n\n* Not fulfilling inclusion criteria\n* Not giving informed consent\n* Living at Læsø or at Bornholm, Denmark\n* Children placed in care outside of the home fulltime in institution of professional family care (the family is not excluded if the children placed in part time in care outside home or fulltime family care within the family)\n* No risk factors found after baseline assessment (as described in the stepped care model) at baseline - these families can be re-referred if their situation changes.\n* Ongoing intensive family treatment in the municipality (for example staying at an institution for parental evaluation by the authorities)?","0 Years","17 Years",{"count":181,"type":22},1452,[25],"VIA Family 2.0 - a Family Based Intervention for families with parental mental illness\n\nBackground: Children born to parents with mental illness have consistently been shown to have increased risks for a range of negative life outcomes including increased frequencies of mental disorders, somatic disorders, poorer cognitive functioning, social, emotional and behavioral problems and lower quality of life. Further these children are often overlooked by both society and mental health services, although they represent a potential for prevention and early intervention.\n\nA collaboration between researchers and clinicians from two regions, the Capital Region and the North Region Denmark has been established as the Research Center for Family Based Interventions. The research center is an umbrella for a series of research activities, all focusing on children and adolescents in families with parental mental illness.\n\nMethod: A large randomized, controlled trial (RCT) for families with parental mental illness will be conducted in order to evaluate the effect of a two-year multidisciplinary, holistic team intervention (the VIA Family 2.0 team intervention) against treatment as usual (TAU). Inclusion criteria will be biological children 0-17 of parents with any mental disorder treated in the secondary sector at any time of their life and receiving treatment in primary or secondary sector within the previous three years. A total of 870 children or approx. 600 families will be included from two sites. Primary outcomes will be changes in child well being, parental stress, family functioning and quality of the home environment, .\n\nTime plan: The RCT will start including families from March 1st, 2024 to Dec 2025 (or later if needed). All families will be assessed at baseline and at end of treatment, i.e. after 24 months and after 36 months. Baseline data will inform the intervention team about each family's needs, problems, and motivation. TAU will be similar in the two regions, which means three family meetings and option for children to participate in peer groups.\n\nChallenges: final funding is being applied for. Recruitment of families can be challenging but we have decades of experience in conducting research in the field. Since both the target group, their potential problems and the intervention is complex, primary outcome is difficult to determine.",[185,186,187,188,31],"Child","Parents","Mental Disorder","Child of Impaired Parents",[190,191,192,193,194],"family based intervention","early intervention","familial high risk","COPMI - children of parents with mental illness","parental mental illness","2024-10-23",{"date":197,"type":70},"2024-10-26",{"date":199,"type":70},"2024-03-18",{"date":201,"type":22},"2028-12-31",{"name":203,"class":113},"Mental Health Centre Copenhagen, Bispebjerg and Frederiksberg Hospital",{"id":205,"slug":206,"hasResults":11,"nctId":207,"briefTitle":208,"officialTitle":209,"acronym":210,"eligibilityCriteria":211,"healthyVolunteers":11,"sex":18,"minAge":212,"maxAge":179,"enrollmentInfo":213,"targetDuration":4,"studyType":23,"phases":215,"briefSummary":216,"conditions":217,"keywords":219,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":223,"lastUpdatePostDateStruct":224,"startDateStruct":226,"completionDateStruct":228,"leadSponsor":230,"locationsCount":232},"100465095","pcom2---the-physician-communication-intervention-version-20-100465095","NCT05336240","PCOM2 - The Physician Communication Intervention, Version 2.0","PCOM2 - The Physician Communication Intervention, Version 2.0\" for \"Linking the Provider Recommendation to Adolescent HPV Vaccine Uptake\"","PCOM2","Inclusion Criteria:\n\n* Parents: Have an adolescent between the ages of 9-17 years old and receiving adolescent care at an enrolled clinic\n* Providers: All providers at participating study practices will be eligible to participate.\n\nExclusion Criteria:\n\n* Parents: Does not have an adolescent between the ages of 9-17 years old and is not receiving adolescent care at an enrolled clinic\n* Providers: Providers who are not at participating study practices","9 Years",{"count":214,"type":22},120,[25],"Poor quality of primary care providers' vaccine recommendations lead to low adolescent human papillomavirus vaccination rates and hundreds of thousands of adolescents unnecessarily at risk for HPV-associated cancers and diseases. Though a previous provider communication intervention, called PCOM, was found to be effective for increasing adolescent HPV vaccination in primary care, its dissemination is limited by the need for significant research team involvement to teach providers how to use the intervention's components. To address this, investigators propose to develop and test a virtual version of PCOM, use mixed methods to assess contextual factors affecting its use compared to the original PCOM intervention, and develop an optimized version of PCOM for broad dissemination to increase adolescent HPV vaccination nationally.",[218,31],"HPV Infection",[220,221,222],"Immunization","Provider Communication","HPV Prevention","2024-08-22",{"date":225,"type":70},"2024-08-26",{"date":227,"type":70},"2023-11-15",{"date":229,"type":22},"2026-12-31",{"name":231,"class":113},"University of Colorado, Denver",2]