[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"health-promotion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:health-promotion":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,19,0,[8,45,97,124,158,194,227,249,271,299,337,375,401,424,453,489,515,543,568],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100053312","a-randomized-control-trial-of-conversations-advancing-resilience-and-empowerment-care-intervention-100053312",false,"NCT07698964","A Randomized Control Trial of Conversations Advancing Resilience and Empowerment (CARE) Intervention","A Randomized Control Trial of Conversations Advancing Resilience and Empowerment (CARE): A Peer-Led Intervention to Improve Health Among Communities in Texas","CARE","Inclusion Criteria:\n\n* Females between the ages of 18-49\n* Self-report at least one risk factor cardiovascular disease (e.g. high blood pressure, high cholesterol, diabetes, overweight, and family history of heart disease).\n* Reside in one of the priority communities will be eligible to participate in the study.\n* Meet minimum digital literacy criteria, defined as having a working and readily accessible email address and using a smart device daily for texting, calling, and checking email.\n\nPriority communities for the South Texas site include Harris, Hidalgo, Cameron, Willacy, Starr, and Nueces counties plus surrounding coastal communities served by South Coastal AHEC.\n\nExclusion Criteria:\n\n* Those not meeting the inclusion criteria will not be eligible to participate",true,"FEMALE","18 Years","49 Years",{"count":22,"type":23},200,"ESTIMATED","INTERVENTIONAL",[26],"NA","The investigators propose to implement and evaluate the effectiveness of the peer-led CARE Intervention designed to mitigate health differences among rural and low-income communities in Texas. This intervention leverages the expertise of Community Health Workers (CHWs) to empower rural and low-income communities, improving health outcomes through outreach, education, counseling, and social support.",[29,30,31],"Quality of Life","Health Promotion","Blood Pressure Monitoring, Self","RECRUITING","2026-07-07",{"date":35,"type":36},"2026-07-13","ACTUAL",{"date":38,"type":36},"2026-06-02",{"date":40,"type":23},"2027-03-31",{"name":42,"class":43},"University of Texas Rio Grande Valley","OTHER",2,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":17,"sex":52,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":24,"phases":57,"briefSummary":58,"conditions":59,"keywords":66,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":96},"100641316","randomized-controlled-trial-of-text-message-to-increase-pneumococcal-vaccination-in-adults-in-chile-100641316","NCT07659470","RANDOMIZED CONTROLLED TRIAL OF TEXT MESSAGE TO INCREASE PNEUMOCOCCAL VACCINATION IN ADULTS IN CHILE.","RANDOMIZED CONTROLLED TRIAL OF THE USE OF TEXT MESSAGE REMINDERS TO INCREASE PNEUMOCOCCAL VACCINATION COVERAGE IN ADULTS AGED 65 YEARS IN CHILE.","Inclusion Criteria:\n\n* Adults born during the year 1961, turning 65 years of age in 2026\n* Resident in Chile at the time of the study\n* Valid mobile phone number registered in the National Immunization Registry (RNI)\n\nExclusion Criteria:\n\n* Record of pneumococcal vaccination in the National Immunization Registry (RNI).\n* Identified as deceased in the Chilean Civil Registry and Identification Service.","ALL","64 Years","65 Years",{"count":56,"type":23},43000,[26],"The goal of this randomized controlled trial is to learn if text message reminders sent through WhatsApp increase pneumococcal vaccination coverage in adults turning 65 years old in Chile. The main questions it aims to answer are:\n\nDo text message reminders increase the proportion of adults aged 65 years who receive the pneumococcal vaccine compared to usual care? Do text message reminders increase pneumococcal vaccination coverage within the first 7 days after the message is sent? Is there an association between socioeconomic factors and pneumococcal vaccination coverage in adults aged 65 years in Chile?\n\nResearchers will compare adults who receive a text message reminder to adults who receive no reminder (usual care) to see if the reminders increase vaccination uptake.\n\nParticipants will:\n\nBe randomly assigned to receive a WhatsApp text message reminder about the pneumococcal vaccine or to receive no reminder Receive a second reminder on day 14 if they have not yet been vaccinated (intervention group only) Be followed for 6 weeks, with vaccination status checked at days 7, 21, and 42 from the start of the intervention",[60,61,62,63,64,30,65],"Pneumococcal Infections","Immunization Programs","Vaccination Coverage","Text Messaging (Intervention)","Reminder Systems","Aged 65 Years or Older",[67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85],"Pneumococcal vaccine","Vaccination coverage","Text message reminder","WhatsApp","Older adults","National Immunization Program","Randomized controlled trial","Health behavior nudge","Digital health intervention","Public health","Streptococcus pneumoniae","Behavioral intervention","Vaccine uptake","Low-cost intervention","Population-based intervention","Pneumococcal polysaccharide vaccine","Immunization registry","Latin America","Chile","NOT_YET_RECRUITING","2026-06-15",{"date":89,"type":36},"2026-06-22",{"date":91,"type":23},"2026-07-15",{"date":93,"type":23},"2026-10-01",{"name":95,"class":43},"Pablo Tomás Valenzuela García",1,{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":102,"acronym":103,"eligibilityCriteria":104,"healthyVolunteers":17,"sex":52,"minAge":19,"maxAge":54,"enrollmentInfo":105,"targetDuration":4,"studyType":24,"phases":106,"briefSummary":107,"conditions":108,"keywords":111,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":96},"100639143","digital-engagement-for-lifelong-health-100639143","NCT07612852","Digital Engagement for Lifelong Health","Digital Engagement for Lifelong Prevention and Health Improvement","DELPHI","Inclusion Criteria:\n\n* Apparent good general health status, confirmed by medical history and initial self-assessment.\n* Ability to understand the study information and provide informed consent.\n* Availability and motivation to participate for the entire duration of the study (12 months).\n* Access to a smartphone compatible with the DELPHI application.\n* Willingness to wear the wearable devices for continuous monitoring of physiological parameters.\n* Basic familiarity with mobile applications or willingness to receive training on their use.\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Presence of severe chronic diseases in active phase (e.g., oncological, cardiovascular, or neurological diseases).\n* Acute or unstable conditions that could compromise participation in the protocol.\n* Current pregnancy.\n* Diagnosed major cognitive or psychiatric disorders that hinder understanding of or adherence to the protocol.\n* Current use of medications that significantly affect the parameters being monitored (e.g., psychotropic drugs, beta-blockers).\n* Simultaneous participation in other clinical studies.\n* Logistical difficulties that prevent frequent interaction with the platform (e.g., lack of connection, unwillingness to attend periodic follow-ups).",{"count":22,"type":23},[26],"The DELPHI project (Digital Engagement for Lifelong Prevention and Health Improvement) aims to develop, implement, and validate an advanced digital platform for promoting well-being and personalized prevention of chronic non-communicable diseases in healthy adults. By integrating wearable sensors, artificial intelligence, federated learning, and the Human Digital Twin (HDT) paradigm, the DELPHI platform is designed to collect, analyze, and interpret multidimensional data in order to deliver dynamic and personalized recommendations for healthy lifestyles.\n\nThe study adopts a multicenter, randomized controlled pilot design, with a maximum duration of 12 months per participant. A total of 200 healthy adults aged 18-65 will be recruited in Southern Italy (Sicily, Campania, and Basilicata) and randomly assigned to either: (1) an experimental group using the full DELPHI platform, including personalized recommendations, adaptive content, and continuous feedback; or (2) a control group using a basic version limited to passive monitoring.\n\nAs a non-clinical primary prevention pilot study, DELPHI aims to assess the operational feasibility, usability, and acceptability of the platform in real-world settings, while also exploring preliminary signals of impact on health and lifestyle domains without confirmatory purposes. Secondary objectives include monitoring physiological indicators, adherence to the app and wearable devices, and evaluating the feasibility of implementing the platform in workplace environments.\n\nData collection will rely on wearable devices, digital questionnaires, and behavioral analysis, with strong safeguards for personal data protection in compliance with GDPR and advanced security approaches such as federated learning and encryption.\n\nSpecific subgroups, including workers from the Fondazione Don Carlo Gnocchi (FDG) as well as university staff and students, will be involved in targeted assessments related to mental well-being and distress. In addition, workers from the FDG will test a virtual reality module designed to evaluate biomechanical overload risks during manual handling activities in simulated environments. These additional physiological and virtual reality components are exploratory and non-diagnostic.\n\nOverall, DELPHI seeks to provide a solid foundation for the adoption of predictive and personalized models in digital health, contributing to the development of a sustainable and accessible prevention ecosystem, particularly in Southern Italy.",[109,110,30],"Life Style, Healthy","Risk Reduction",[112,113,114],"health","digitalization","prevention","2026-05-25",{"date":117,"type":36},"2026-05-29",{"date":119,"type":36},"2026-05-04",{"date":121,"type":23},"2027-03-30",{"name":123,"class":43},"Istituto per la Ricerca e l'Innovazione Biomedica",{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":128,"acronym":4,"eligibilityCriteria":129,"healthyVolunteers":17,"sex":52,"minAge":130,"maxAge":19,"enrollmentInfo":131,"targetDuration":4,"studyType":24,"phases":133,"briefSummary":134,"conditions":135,"keywords":143,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":149,"lastUpdatePostDateStruct":150,"startDateStruct":152,"completionDateStruct":154,"leadSponsor":156,"locationsCount":96},"100613449","pursuit-a-technologically-augmented-school-based-program-to-improve-child-coping-and-prevent-substance-use-100613449","NCT07266740","PURSUIT: A Technologically Augmented School-based Program to Improve Child Coping and Prevent Substance Use.","Inclusion Criteria:\n\n* Aged eight to 18 years\n* Enrolled in a Michigan elementary, middle, or high school\n\nExclusion Criteria:\n\n* Age under 8\n* Age over 18 years\n* Non-enrollment in A Michigan school.","8 Years",{"count":132,"type":23},100,[26],"The study investigators aim to test an online support platform for Michigan youth aged 8-18 years enrolled in elementary, middle, or high school and their parent\u002Fcaregiver. The online support platform will be hosted on the Computerized Intervention Authoring System (CIAS) 3.0 and will provide evidence-based cognitive behavioral coping skills for physical (pain) and mental (stress, mood) health symptoms, with additional substance use prevention content for youth aged 12 and older. Evaluations will occur at baseline and then a post assessment approximately 8 weeks later.",[136,137,138,139,140,141,30,142],"Pediatric Pain","Anxiety","Mood","Stress","Feasibility Studies","Acceptability","Online Mental Health Program",[144,145,146,139,147,137,138,148],"Cognitive-behavioral","School","Pediatrics","Pain","Substance use","2026-05-05",{"date":151,"type":36},"2026-05-07",{"date":153,"type":23},"2026-05-01",{"date":155,"type":23},"2026-10",{"name":157,"class":43},"Michigan State University",{"id":159,"slug":160,"hasResults":11,"nctId":161,"briefTitle":162,"officialTitle":163,"acronym":164,"eligibilityCriteria":165,"healthyVolunteers":17,"sex":52,"minAge":166,"maxAge":167,"enrollmentInfo":168,"targetDuration":4,"studyType":24,"phases":170,"briefSummary":171,"conditions":172,"keywords":177,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":192,"locationsCount":96},"100576989","eplatform-for-promoting-health-in-schools-100576989","NCT06792461","ePlatform for Promoting Health in Schools","A Randomized Controlled Trial to Evaluate the Implementation of an eHealth Platform for Promoting Healthy Habits Among Adolescents From Socially Disadvantaged Settings: the ePro-Schools Project","ePro-Schools","Inclusion Criteria\n\nAdolescents:\n\n* Students enrolled in 1st, 2nd, or 3rd year of ESO (ages approximately 11-16) at participating secondary schools located in the Central Catalonia region, particularly those in socially disadvantaged settings.\n* All genders will be eligible.\n* Written informed consent must be provided by both the adolescent and their parent(s)\u002Flegal guardian(s).\n\nPhysical Education Teachers:\n\n* Physical education teachers currently working at the participating secondary schools.\n* Must be 18 years of age or older.\n* Must provide written informed consent to participate.\n\nExclusion Criteria\n\n* Individuals (adolescents or teachers) who do not provide written informed consent will be excluded.\n* No other exclusion criteria will be applied.","11 Years","16 Years",{"count":169,"type":23},1000,[26],"There are few public health and educational policies specifically aimed at promoting physical activity, healthy dietary habits, and reducing sedentary behaviour among adolescents from socially disadvantaged backgrounds. ePro-Schools will co-design, pilot and evaluate an evidence-based program, delivered via a modular eHealth platform, to promote physical activity and healthy eating, and reduce time in sedentary behaviours. A profound co-creation process involving adolescents, school staff, and policymakers-alongside the adaptation of previous interventions by consortium members-will support the program's development. The ePro-Schools platform will contain modules for adolescents and their parents, teachers and school administration. Although the platform will be implemented through schools, it will include content to be implemented outside the school setting. The intervention program will be evaluated through a randomised controlled trial conducted in six secondary schools in Central Catalonia that aims to include 1000 adolescents. Schools have been randomised (1:1) into an intervention and a waiting-list control group.\n\nThe evaluation of the program includes effectiveness, cost-effectiveness and process evaluation. Physical activity, sedentary behaviour and eating habits are the primary effectiveness outcomes of the trial. Secondary outcomes include fitness, water consumption, quality of life, depressive symptoms, social isolation and sleep quality. Using implementation science methodology, ePro-Schools will co-design transferable evidence-based practices and methodologies and guidance for scaling up the platform with policymakers and stakeholders, as well as informing specialists, policymakers and the general public.",[30,173,174,175,176],"Health Education","Physical Activity","Nutrition","Behaviour Change",[178,179,180,181,182,183,184],"eHealth","Adolescents","Socially disadvantaged settings","Randomized control trial","Co-design","School-based interventions","Health promotion","2026-04-23",{"date":187,"type":36},"2026-04-29",{"date":189,"type":36},"2025-09-08",{"date":191,"type":23},"2027-03",{"name":193,"class":43},"Fundació Sant Joan de Déu",{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":4,"eligibilityCriteria":200,"healthyVolunteers":17,"sex":52,"minAge":201,"maxAge":4,"enrollmentInfo":202,"targetDuration":4,"studyType":24,"phases":204,"briefSummary":205,"conditions":206,"keywords":209,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":219,"lastUpdatePostDateStruct":220,"startDateStruct":221,"completionDateStruct":223,"leadSponsor":225,"locationsCount":96},"100634471","social-prescribing-intervention-for-health-promotion-in-community-dwelling-older-adults-100634471","NCT07540117","Social Prescribing Intervention for Health Promotion in Community-Dwelling Older Adults","Social Prescribing for Health Promotion in Community-Dwelling Older Adults: Prospective Cohort Study Combining Mindfulness Meditation and Nordic Walking Pole Exercise","Inclusion Criteria:\n\n* Adults aged 55 years and older\n* Community-dwelling older adults\n* Able to walk independently or with assistive devices\n* Normal cognitive function or mild cognitive impairment, with ability to understand and follow study procedures\n* Willing to sign informed consent\n* Willing to participate in the intervention and complete study assessments\n\nExclusion Criteria:\n\n* Major surgery or hospitalization within the previous 3 months\n* Severe cardiovascular disease or other medical condition making exercise inappropriate, based on physician assessment\n* Moderate to severe dementia or other severe psychiatric disorder\n* Inability to comply with the 4-week mindfulness meditation program or the 12-week walking-pole exercise program","55 Years",{"count":203,"type":23},1500,[26],"This study evaluates the effects of a social prescribing intervention on health promotion outcomes in community-dwelling older adults. The intervention consists of a 4-week mindfulness meditation program followed by a 12-week walking-pole exercise program. The purpose of the study is to determine whether this combined intervention improves physical function, psychological well-being, and sleep quality.\n\nEligible participants aged 55 years and older will be enrolled from community settings and will receive the same 16-week intervention. Assessments will be conducted at baseline, after the mindfulness phase, after completion of the full intervention, and 3 months after the intervention ends. Study outcomes include physical function, mood, well-being, sleep quality, and indicators of continued participation and lifestyle change.\n\nThe investigators hypothesize that the combined social prescribing intervention will lead to improvements in physical and psychological health among community-dwelling older adults and support healthy aging.",[207,30,208],"Aging","Mental Health",[210,211,212,213,214,215,30,216,217,218],"Social Prescribing","Mindfulness Meditation","Walking Pole Exercise","Older Adults","Community-Dwelling Older Adults","Healthy Aging","Psychological Well-Being","Sleep Quality","Physical Function","2026-04-20",{"date":185,"type":36},{"date":222,"type":36},"2026-04-14",{"date":224,"type":23},"2029-04",{"name":226,"class":43},"National Health Research Institutes, Taiwan",{"id":228,"slug":229,"hasResults":11,"nctId":230,"briefTitle":231,"officialTitle":232,"acronym":4,"eligibilityCriteria":233,"healthyVolunteers":17,"sex":234,"minAge":19,"maxAge":4,"enrollmentInfo":235,"targetDuration":4,"studyType":24,"phases":237,"briefSummary":238,"conditions":239,"keywords":4,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":241,"lastUpdatePostDateStruct":242,"startDateStruct":244,"completionDateStruct":245,"leadSponsor":247,"locationsCount":96},"100590224","the-ku-ola-project-enhancing-health-promotion-among-native-hawaiian-men-100590224","NCT06964633","The Ku Ola Project: Enhancing Health Promotion Among Native Hawaiian Men.","The Ku Ola Project","* Inclusion Criteria Self-identified as male At least 18 years of age Hawaii residency Able to read and understand English\n* Exclusion Criteria Under 18 years of age Not proficient in English Any medical condition or situation that, in the investigator's judgment, would make continued participation not in the participant's best interest","MALE",{"count":236,"type":23},600,[26],"The Ku Ola Project: The goal of this study is to determine if community-based discussion groups and small educational sessions enhance health awareness and behaviors among Native Hawaiian men. The study will examine if these interventions improve participants' health knowledge, attitudes, and self-efficacy while fostering local networks to support ongoing health promotion. Participants will engage in group discussions and educational sessions designed to build capacity and encourage healthy lifestyle choices.",[30,240],"Health","2026-03-29",{"date":243,"type":36},"2026-03-31",{"date":153,"type":23},{"date":246,"type":23},"2028-05-31",{"name":248,"class":43},"University of Hawaii",{"id":250,"slug":251,"hasResults":11,"nctId":252,"briefTitle":253,"officialTitle":253,"acronym":4,"eligibilityCriteria":254,"healthyVolunteers":17,"sex":52,"minAge":255,"maxAge":256,"enrollmentInfo":257,"targetDuration":4,"studyType":24,"phases":259,"briefSummary":260,"conditions":261,"keywords":4,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":262,"lastUpdatePostDateStruct":263,"startDateStruct":265,"completionDateStruct":267,"leadSponsor":269,"locationsCount":96},"100627253","reframing-retirement-an-examination-of-identity-change-and-self-regulation-approaches-to-promote-physical-activity-100627253","NCT07446231","Reframing Retirement: An Examination of Identity Change and Self-Regulation Approaches to Promote Physical Activity","Inclusion Criteria:\n\n* Adults aged 60-70 years\n* Recently retired (within the past 1.5 years) from occupational work\n* Access to the internet via computer or smartphone\n* Able to engage in moderate-to-vigorous physical activity (MVPA) independently\n* Participating in less than 150 minutes of MVPA per week, based on:\n\nScreening with Godin's Leisure Time Exercise Questionnaire, and Baseline accelerometry as secondary confirmation\n\nExclusion Criteria:\n\n\\- Participation in 150 minutes or more of MVPA per week, based on questionnaire or accelerometry screening","60 Years","70 Years",{"count":258,"type":23},159,[26],"The primary objective of this clinical trial is to test the efficacy of an innovative multimodal eHealth \\& mHealth intervention (focused on emphasizing identity\u002Fhabit and\u002For self-regulation) on increasing moderate to vigorous (MVPA) across 12 months among newly retired adults not meeting Physical Activity guidelines at study baseline, thus at higher risk of age-related chronic diseases.\n\nThe secondary objectives are to examine whether these approaches improve physical and mental well-being and health related fitness-outcomes.\n\nPrincipal Research Question 1: Does an intervention focused on identity\u002Fhabit + self-regulation skills + education (ID) increase moderate-to-vigorous intensity physical activity (MVPA) compared with an intervention focused on self-regulation skills + education (SR), and an education control condition (ED)? Three-arm parallel design single blinded randomized controlled trial. Participants will be randomized to one of three groups (ID, SR, ED) for 12 months duration.\n\n* After the initial screening process, eligible participants will be provided with an accelerometer-mailed or delivered in person-to wear for seven consecutive days. Data collected will verify baseline physical activity levels and determine final eligibility based on adherence to physical activity guideline thresholds.\n* Participants will visit the lab for fitness testing and complete an online questionnaire See below in \"detailed description\" the breakdown\u002Fdelivery given for each of the 3 arms.",[174,30],"2026-02-25",{"date":264,"type":36},"2026-03-03",{"date":266,"type":23},"2026-03-01",{"date":268,"type":23},"2030-03-31",{"name":270,"class":43},"University of Victoria",{"id":272,"slug":273,"hasResults":11,"nctId":274,"briefTitle":275,"officialTitle":276,"acronym":277,"eligibilityCriteria":278,"healthyVolunteers":11,"sex":52,"minAge":19,"maxAge":4,"enrollmentInfo":279,"targetDuration":4,"studyType":24,"phases":281,"briefSummary":282,"conditions":283,"keywords":286,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":289,"lastUpdatePostDateStruct":290,"startDateStruct":292,"completionDateStruct":294,"leadSponsor":296,"locationsCount":298},"100580892","teaching-health-resilience-in-a-hospital-setting-a-peer-led-intervention-100580892","NCT06843213","Teaching Health Resilience in a Hospital Setting: A Peer-led Intervention","Teaching Health Promotion and Resilience in Varied Environments: a Peer-led Intervention Following Hospital Discharge","THRIVE","Inclusion Criteria:\n\n* Participants who are: a) admitted to University of Pittsburgh Medical Center (UPMC) Shadyside Hospital, UPMC Presbyterian-Montefiore Hospital, UPMC Mercy Hospital for inpatient or observation status, or b) seen in the Emergency Department setting at UPMC Presbyterian-Montefiore Hospital and UPMC Mercy Hospital.\n* Participants must have a current diagnosis of Opioid Use Disorder based on the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) diagnostic criteria.\n* Participants must be at least 18 years of age on day of admission.\n* Participants must be able to speak and read English.\n\nExclusion Criteria:\n\n* Participants diagnosed with dementia and\u002For cognitive impairments.\n* Participants with acute psychiatric complications, such as schizophrenia with acute psychosis, acute mania, or suicidal ideation (which may impact the ability of a participant to consent and actively participate in treatment).\n* Participants who are pregnant or lactating at onset of study.\n* Participants who cannot read or speak English.",{"count":280,"type":23},390,[26],"The purpose of the study is to develop an acceptable, feasible, and effective peer-led bundle of health resilience and promotion services to be delivered in the hospital setting, called the THRIVE intervention.\n\nThe main question it aims to answer is: Will participants receiving the THRIVE intervention have a reduced risk of self-reported non-fatal overdoses OR skin\u002Fsoft tissue infections compared to participants receiving enhanced usual care?\n\nResearchers will compare the THRIVE model to enhanced usual care to see if the THRIVE model helps participants reduce their number of self-reported non-fatal overdoses OR skin\u002Fsoft tissue infections.\n\nIntervention participants will:\n\n* Receive one in-person session from a peer support specialist while in the hospital\n* Receive weekly text messages from the peer support specialist for a 12-week period\n* Receive monthly, multiple-choice assessments via text message at Month 1, 2, 3, 4, 5, and 6\n* Complete a baseline, 3-month, and 6-month assessment with Research Assistants\n\nEnhanced usual care participants will:\n\n* Receive a handout with health resilience education and resources in their local area\n* Receive monthly, multiple-choice assessments via text message at Month 1, 2, 3, 4, 5, and 6\n* Complete a baseline, 3-month, and 6-month assessment with Research Assistants",[284,285,30],"Opioid Use Disorder","Harm Reduction",[284,285,287,288],"Peer Support","Peer Support Specialists","2026-02-24",{"date":291,"type":36},"2026-02-27",{"date":293,"type":36},"2025-02-18",{"date":295,"type":23},"2028-08-01",{"name":297,"class":43},"University of Pennsylvania",3,{"id":300,"slug":301,"hasResults":11,"nctId":302,"briefTitle":303,"officialTitle":304,"acronym":4,"eligibilityCriteria":305,"healthyVolunteers":17,"sex":52,"minAge":306,"maxAge":307,"enrollmentInfo":308,"targetDuration":4,"studyType":24,"phases":310,"briefSummary":311,"conditions":312,"keywords":318,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":328,"lastUpdatePostDateStruct":329,"startDateStruct":331,"completionDateStruct":333,"leadSponsor":335,"locationsCount":44},"100622607","a-comparative-intervention-study-on-strategies-for-fruit-distribution-and-awareness-campaigns-in-schools-100622607","NCT07385820","A Comparative Intervention Study on Strategies for Fruit Distribution and Awareness Campaigns in Schools","An Interventional Study Evaluating Two Different School Deployment Strategies, Testing the Effects of Onsite Awareness Raising on the Adoption of the Fruit-stands by Local Student Populations","Inclusion Criteria:\n\n* Students enrolled in a Swedish school (elementary, middle, or high school)\n* Ages 7-19 years\n* Able to use a mobile phone to document meals and snacks\n* Provided informed consent (with parental consent required for participants under 15 years old)\n\nExclusion Criteria:\n\n\\- Presence of any clinically significant disease or condition that, in the opinion of the research team, may interfere with participation or influence study outcomes","7 Years","19 Years",{"count":309,"type":23},300,[26],"This implementation study evaluates two strategies to increase fruit consumption among Swedish students. (1) installing fruit stands in schools and (2) combining fruit stands with a health-awareness campaign. The intervention is implemented in a set of participating schools, each following one of the predefined strategies. Students are asked to use a research app to photograph their meals and snacks during three data-collection periods before, during, and after the intervention. The study collects information on fruit intake, eating patterns, and the number of fruits taken from the stands to assess effectiveness and reduce food waste. The aim is to identify which strategy better supports healthy eating habits in school environments.",[313,314,315,316,30,317],"Dietary Behaviors","Fruit Consumption","Dietary Habits","Healthy Eating","Schools",[319,320,321,322,145,184,323,324,325,326,76,327],"Healthy eating","Dietary behavior","Fruit consumption","School environment","Prevention","Behavior change","Implementation study","School-based intervention","Adolescent health","2026-02-04",{"date":330,"type":36},"2026-02-06",{"date":332,"type":36},"2026-01-12",{"date":334,"type":23},"2026-12-31",{"name":336,"class":43},"Karolinska Institutet",{"id":338,"slug":339,"hasResults":11,"nctId":340,"briefTitle":341,"officialTitle":342,"acronym":343,"eligibilityCriteria":344,"healthyVolunteers":17,"sex":52,"minAge":19,"maxAge":255,"enrollmentInfo":345,"targetDuration":4,"studyType":24,"phases":347,"briefSummary":348,"conditions":349,"keywords":351,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":366,"lastUpdatePostDateStruct":367,"startDateStruct":369,"completionDateStruct":371,"leadSponsor":373,"locationsCount":96},"100613099","dance-mindfulness-intervention-for-well-being-in-recreational-adults-100613099","NCT07262177","Dance-Mindfulness Intervention for Well-Being in Recreational Adults","Mindful Embodied Movement: A 12-Week Modern Dance-Mindfulness Intervention and Mixed-Methods Randomized Controlled Trial in Recreational Adult Dancers","DanceMind","Inclusion Criteria:\n\n* Adults aged 18 years and older\n* Enrolled in dance classes (preferring modern\u002Fcontemporary) at participating schools for at least 6 months prior to study enrollment\n* Able and willing to attend weekly sessions for 12 consecutive weeks (minimum 70% attendance required)\n* Able to understand and complete study questionnaires in Greek language\n* Able to engage in moderate-intensity movement and dance activities without acute medical contraindications\n* Written informed consent provided\n* Willing to be randomly assigned to intervention or waitlist control group\n\nExclusion Criteria:\n\n* Musculoskeletal or neurological conditions limiting safe participation in moderate-intensity movement (e.g., acute injury, severe arthritis, neurological disease affecting coordination\u002Fbalance)\n* Current severe psychological distress or mental health crisis requiring immediate clinical intervention (screened via DASS-21; cutoff: Severe or Extremely Severe on any subscale)\n* Pregnancy or planning pregnancy during the 12-week study period\n* Current concurrent participation in other psychological interventions, therapy, or mind-body programs (Pilates, yoga, tai-chi, other mindfulness-based interventions)\n* Unable to attend ≥70% of weekly sessions due to scheduling constraints or anticipated absences\n* Inability to provide informed consent or complete questionnaires in Greek\n* Acute medical illness or hospitalization within 2 weeks of study start\n* History of substance abuse disorder currently active or untreated",{"count":346,"type":23},160,[26],"This 12-week study protocol outlines a randomized controlled trial designed to evaluate the effectiveness of a Dance-Mindfulness intervention integrating Modern Theatre Dance with mindfulness-based embodied practices to enhance psychological wellbeing, nervous system regulation, and embodied awareness in adults. The intervention combines: (1) polyvagal-informed breath-movement synchronization (nasal breathing, grounding); (2) ISTD (Imperial Society of Teachers of Dancing) Modern Theatre Dance technique progression and dance movements (Grades 2-4); (3) nervous system regulation through somatic practices; and (4) phenomenological reflection via weekly journaling and post-session integration.\n\nStudy Design: Parallel-assignment randomized controlled trial (approx. N=320; n=160 intervention, n=160 waitlist control). Randomization uses computer-generated block randomization (block sizes 4-6).\n\nOutcomes: Perceived stress, mindfulness psychological wellbeing (happiness, life satisfaction), emotional regulation, social connection, movement confidence.\n\nQualitative Component: Phenomenological interviews and weekly reflective journals from subsample (approx. n=20) analyzed via Interpretative Phenomenological Analysis and Reflexive Thematic Analysis.\n\nIntervention Delivery: 90-100 minute weekly sessions delivered over 12 weeks by qualified facilitator(s) trained in Modern Theatre Dance, mindfulness (≥3 years personal practice, MBSR, yoga or equivalent), trauma-informed care, and group facilitation. Sessions include 8 structured components: breath-grounding (9-10 min), technical dance work (14-15 min), conditioning (9-10 min), break-settling (4-5 min), rhythm improvisation (8-9 min), choreographed sequences (15-17 min), cool-down-integration (8-9 min), and phenomenological journaling (10-20 min).\n\nSafety \\& Fidelity: Structured facilitator guidelines, session checklists, weekly supervision, adverse event protocols, and external fidelity monitoring ensure protocol integrity. Classroom size: 15-18 participants per session.\n\nData Collection: Baseline (Week 0), mid-intervention (Week 6 only for qualitative), post-intervention (Week 12), and optional 1-3 month follow-up. Intent to treat analysis and mixed-effects modeling for between-group comparisons. Population: Adults (age 18+) seeking wellbeing enhancement through recreation or stress reduction. Eligible participants without acute mental health crisis. Primary Purpose: Health promotion and mental health improvement through nervous system regulation, embodied awareness, and psychosocial wellbeing enhancement.",[350,30],"Healthy Volunteers",[352,353,354,355,356,357,358,359,360,361,362,363,364,365],"somatic education","embodied phenomenology","community-based dance education","dance movement therapy","psychological wellbeing","mindfulness","creative movement","interoception","autonomic regulation","embodied awareness","emotional regulation","vagal regulation","stress reduction","motor learning","2026-01-01",{"date":368,"type":36},"2026-01-06",{"date":370,"type":36},"2025-09-02",{"date":372,"type":23},"2026-05-31",{"name":374,"class":43},"University of Thessaly",{"id":376,"slug":377,"hasResults":11,"nctId":378,"briefTitle":379,"officialTitle":380,"acronym":4,"eligibilityCriteria":381,"healthyVolunteers":11,"sex":52,"minAge":19,"maxAge":4,"enrollmentInfo":382,"targetDuration":4,"studyType":24,"phases":384,"briefSummary":385,"conditions":386,"keywords":388,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":392,"lastUpdatePostDateStruct":393,"startDateStruct":395,"completionDateStruct":397,"leadSponsor":399,"locationsCount":96},"100611435","xylitol-gum-for-promoting-smoking-cessation-100611435","NCT07240545","Xylitol Gum for Promoting Smoking Cessation","The Effectiveness of Chewing Gum for Reducing Cigarette Consumption and Promoting Smoking Cessation: A Pilot Randomized Controlled Trial","Inclusion Criteria:\n\n* Residents of Hong Kong aged 18 or above who smoke at least 1 cigarette per day over the past 3 months\n* Have the habit of chewing gum or are willing to use chewing gum\n* Can communicate in Cantonese (including reading Chinese)\n* Express an intention to quit or reduce smoking\n* Capable of using instant messaging tools (e.g., WhatsApp, WeChat) for communication\n\nExclusion Criteria:\n\n* Have communication barriers (either physical or cognitive)\n* Currently participating in other smoking cessation programs or services",{"count":383,"type":23},134,[26],"The goal of this clinical trial is to learn if 4-week xylitol gum intervention works to promote smoking cessation in daily smokers. It will also learn about the feasibility and acceptability of using xylitol gum. The main questions it aims to answer are:\n\n（1）Does xylitol gum help to reduce cigarette consumption and promote smoking cessation?\n\nResearchers will compare 4-week xylitol gum intervention to the brief advice to see if xylitol gum works to promote smoking cessation.\n\nParticipants in the intervention group will receive a 3-month behavioral intervention comprising a 4-week xylitol gum aligned with 12 weeks of instant reminder message support.",[387,30],"Smoking Cessation",[389,390,391],"Xylitol gum","Smoking cessation","Hybrid type 1 effectiveness-implementation design","2025-11-16",{"date":394,"type":36},"2025-11-21",{"date":396,"type":23},"2025-11-24",{"date":398,"type":23},"2026-09-30",{"name":400,"class":43},"The University of Hong Kong",{"id":402,"slug":403,"hasResults":11,"nctId":404,"briefTitle":405,"officialTitle":406,"acronym":4,"eligibilityCriteria":407,"healthyVolunteers":17,"sex":52,"minAge":19,"maxAge":4,"enrollmentInfo":408,"targetDuration":4,"studyType":410,"phases":4,"briefSummary":411,"conditions":412,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":415,"lastUpdatePostDateStruct":416,"startDateStruct":418,"completionDateStruct":420,"leadSponsor":422,"locationsCount":96},"100606330","qualitative-study-among-migrant-and-socially-vulnerable-populations-on-their-interest-in-collective-approaches-to-health-promotion-100606330","NCT07174154","Qualitative Study Among Migrant and Socially Vulnerable Populations on Their Interest in Collective Approaches to Health Promotion.","Despite Socio-economic, Cultural, and Institutional Barriers: How Can Migrant and Socially Vulnerable Populations Who Visit The World Doctors in Nice be Involved in Collective Health Promotion Initiatives? An Exploratory Qualitative Study Based on Semi-structured Interviews.","Inclusion Criteria:\n\n* Age ≥ 18 years.\n* Sufficient understanding and expression in French to answer the questions.\n* Migrant or socially vulnerable user attending the Médecins du Monde CASO (Reception, Care and Orientation Center) in Nice.\n* Willing to participate in the interview (oral consent provided)\n\nExclusion Criteria:\n\n* Minor (\\\u003C 18 years).\n* Non-French-speaking.\n* Refusal to participate.",{"count":409,"type":23},10,"OBSERVATIONAL","This exploratory qualitative study aims to collect the health needs and representations of migrant and socially vulnerable populations attending the Doctors in the World center in Nice, and to assess their interest in collective approaches to health promotion. Semi-structured interviews were conducted between June and August 2025. Data are analyzed thematically to identify needs, barriers and facilitators to the implementation of collective health groups",[30,413,414],"Vulnerable Populations","Access to Health Care","2025-09-11",{"date":417,"type":36},"2025-09-15",{"date":419,"type":36},"2025-06-01",{"date":421,"type":23},"2026-01-31",{"name":423,"class":43},"Centre Hospitalier Universitaire de Nice",{"id":425,"slug":426,"hasResults":11,"nctId":427,"briefTitle":428,"officialTitle":429,"acronym":430,"eligibilityCriteria":431,"healthyVolunteers":17,"sex":52,"minAge":432,"maxAge":19,"enrollmentInfo":433,"targetDuration":4,"studyType":24,"phases":434,"briefSummary":435,"conditions":436,"keywords":439,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":415,"lastUpdatePostDateStruct":445,"startDateStruct":447,"completionDateStruct":449,"leadSponsor":450,"locationsCount":452},"100530006","yopa---a-youth-centred-participatory-action-100530006","NCT06181162","YoPA - A Youth-centred Participatory Action","YoPA - A Youth-centred Participatory Action Approach Towards Co-created Implementation of Socially and Physically Activating Environmental Interventions in Africa and Europe.","YoPA","Inclusion Criteria:\n\n* aged 12 to 18 years\n* living in a disadvantaged area in Aalborg (Denmark), Amsterdam (the Netherlands), Osogbo (Nigeria), or Soweto (South Africa)\n* active informed consent by the adolescents and at least one parent\u002Fcaregiver where applicable for the participation of the adolescent\n\nExclusion Criteria:\n\n* none","12 Years",{"count":169,"type":23},[26],"Background\n\nA vast majority of adolescents do not meet guidelines for healthy physical activity, sedentary behaviour, and sleep, posing major risks for developing multiple non-communicable diseases. Unhealthy lifestyles seem more prevalent in urban than rural areas, with the neighbourhood environment as a mediating pathway linking urban living and poor health. How to develop and implement sustainable and effective interventions focused on adolescent health and wellbeing in urban vulnerable life situations is a key challenge and research gap. This paper describes the protocol of a Youth-centred Participatory Action (YoPA) project aiming to tailor, implement, and evaluate social and physical environmental interventions using an evidence-informed youth-centred co-creation approach, for structural improvement of the lifestyles of adolescents in urban vulnerable life situations.\n\nMethods\n\nIn diverse urban environments in Denmark, the Netherlands, Nigeria, and South Africa, academic researchers will engage adolescents (12-19 years) growing up in vulnerable life situations and other key stakeholders (e.g., policy makers, urban planners, community leaders) in local co-creation communities. Together with academic researchers and local stakeholders, adolescents will take a leading role in mapping the local system for needs and opportunities; tailoring interventions to their local context; implementing and evaluating interventions during participatory meetings over the course of three years. YoPA applies a participatory mixed methods design guided by the newly developed SUPER-AIM framework assessing: (i) the local Systems, (ii) User perspectives, (iii) the Participatory co-creation process, (ii) Effects, iv) Reach, (vi) Adoption, (vii) Implementation, and (viii) Maintenance of interventions, in an integrated manner.\n\nDiscussion\n\nYoPA aims to fill various research gaps, including the development of a practical protocol guiding the application of co-creation to tailor evidence-informed interventions to divers, multi-country contexts. Additionally, it focuses on advancing the research gap in physical activity and health within Sub-Saharan Africa and the involvement of adolescents in shaping their physical and social environments. Academic researchers envision that the YoPA co-creation approach will serve as a guide for participation of adolescents in vulnerable life situations in implementation of health promotion and urban planning in Europe, Africa and globally.",[174,30,437,438],"Sleep","Screen Use",[440,30,441,179,442,443,444],"Participatory Action Research","Systems Approach","24-hour movement behaviour","Physical activity","Urban health",{"date":446,"type":36},"2025-09-17",{"date":448,"type":36},"2023-11-01",{"date":334,"type":23},{"name":451,"class":43},"Amsterdam UMC, location VUmc",4,{"id":454,"slug":455,"hasResults":11,"nctId":456,"briefTitle":457,"officialTitle":458,"acronym":459,"eligibilityCriteria":460,"healthyVolunteers":11,"sex":52,"minAge":432,"maxAge":461,"enrollmentInfo":462,"targetDuration":4,"studyType":24,"phases":464,"briefSummary":465,"conditions":466,"keywords":475,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":481,"lastUpdatePostDateStruct":482,"startDateStruct":484,"completionDateStruct":485,"leadSponsor":487,"locationsCount":96},"100587090","controlled-evaluation-of-an-exercise-program-for-overweight-adolescents-100587090","NCT06923865","Controlled Evaluation of an Exercise Program for Overweight Adolescents","Now! Project - a Controlled Evaluation of a Physical Activity Program for Adolescents With Overweight","Now!","Inclusion Criteria:\n\n* BMI above the 90th percentile for their age and gender (WHO reference table)\n* Deficits in movement motivation and motor skills\n* No health complaints or movement-restricting conditions\n* No health risks for maximal exertion\n* Ability to verbally communicate pain or discomfort\n* Unremarkable PAR-Q questionnaire\n* Signed parental consent form\n\nExclusion Criteria:\n\n* Acute or chronic illness\n* Inability to follow the study procedures (e.g., language barriers, psychological disorders)","14 Years",{"count":463,"type":23},150,[26],"Physical activity decreases as young people get older, especially during the shift from early to late adolescence. Unfortunately, around 81% of school-aged children worldwide between the ages of 11 and 17 do not meet the recommendation of at least one hour of physical activity per day - and this is also true in Switzerland. Not being active enough, whether normal weight or overweight, can lead to long-term health problems and is a major factor in becoming overweight over time. This results in healthcare costs and negatively affects quality of life. Supporting physical activity in overweight youth requires well-rounded, thoughtful programs.\n\nThe investigators studying the impact of the movement programs now! and now!+ on the physical activity and health of young people. The goal is to look at both physical and mental changes equally.\n\nTaking part in this study involves minimal physical or mental risk for the participants. These small risks from the testing methods and activities are taken into account in how the program is explained and carried out.\n\nThe benefits for the participants - feeling healthier and fitter physically, and more confident and capable mentally - clearly outweigh any potential risks, thanks to the additional, guided, and personalized exercise program.\n\nThe participants take part in the now! and now!+ exercise programs run by the Basel-Stadt Sports Office and the DSBG. now! is a 90-minute group session with up to 14 young people, while now!+ is a 90-minute small-group session with 2 to 4 participants. Both programs take place once a week over a 12-month period and pause during school holidays (38 training weeks in total).\n\nEach session includes a warm-up, a strength or endurance training block, and a coordination phase. The program is modular and adapted to the physical and personal needs of each participant. This ensures that overweight adolescents are not overstrained and don't develop symptoms like pain, frustration, or lack of motivation (Behringer et al., 2011), while still allowing for a training stimulus that supports physical improvement.\n\nThe results of the evaluations are directly used to improve and further develop the exercise program. The overall project includes three rounds, each consisting of one year of training and three test sessions, each lasting about two hours. The now! and now!+ programs are held weekly for a total of 38 weeks per year, with breaks during school holidays.\n\nEach of the three test sessions includes the same set of assessments (see \"Study Intervention\") and follows a set order: The process begins with measuring body size and blood pressure, followed by a static retinal vessel analysis. After these medical checks, participants do a 5-minute warm-up on a stationary bike at a set resistance level. Then, strength tests are performed: knee extension on the IsoMed 2000, handgrip strength, and jump power on the Leonardo force plate. The endurance test using spiroergometry marks the end of the physical assessments.\n\nFinally, impulse control is tested, and participants complete a set of questionnaires. At the end of the session, each participant is given an actigraph (a small motion sensor worn on the body) to track their physical activity over the following seven days.",[467,468,469,30,470,471,29,472,473,474],"Adolescent","Pediatric Obesity","Exercise Therapy","Program Evaluation","Impulse Control Disorders","Retinal Vessels","Strength Training Effects","Aerobic Capacity",[476,477,478,479,480],"Overweight adolescents","Youth physical activity","Motor performance in children","Impulse control and fitness","training in peer groups","2025-04-04",{"date":483,"type":36},"2025-04-11",{"date":419,"type":23},{"date":486,"type":23},"2029-12",{"name":488,"class":43},"University Hospital, Basel, Switzerland",{"id":490,"slug":491,"hasResults":11,"nctId":492,"briefTitle":493,"officialTitle":493,"acronym":494,"eligibilityCriteria":495,"healthyVolunteers":17,"sex":52,"minAge":255,"maxAge":4,"enrollmentInfo":496,"targetDuration":4,"studyType":24,"phases":497,"briefSummary":498,"conditions":499,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":506,"lastUpdatePostDateStruct":507,"startDateStruct":509,"completionDateStruct":511,"leadSponsor":513,"locationsCount":96},"100584514","a-service-learning-program-for-comprehensive-geriatric-assessment-and-health-promotion-in-older-adults-100584514","NCT06890325","A Service-Learning Program for Comprehensive Geriatric Assessment and Health Promotion in Older Adults","GEROS","Inclusion Criteria:\n\nA) For users:\n\n* Any person aged 60 or older who can move to the facility (Faculty of Health Sciences and Welfare) independently or accompanied by a caregiver.\n\nB) For students:\n\n* Students from Nursing, Physiotherapy, Nutrition and Dietetics, Occupational Therapy and Psychology degrees of UVic-UCC.\n\nExclusion Criteria:\n\n* For users: Individuals institutionalized in a long-term care institution.",{"count":132,"type":23},[26],"The GEROS Project aims to develop and implement a Service-Learning (S-L) program that integrates Comprehensive Geriatric Assessment (CGA) and health promotion, for students at the Faculty of Health Sciences and Welfare at the University of Vic - Central University of Catalonia (UVic-UCC). This initiative engages university students, healthcare professionals, and older adults (60+) in a participatory, intergenerational approach that fosters mutual learning and community engagement.\n\nThe study follows a non-experimental mixed-method design, involving students from Nursing, Physiotherapy, Human Nutrition and Dietetics, Occupational Therapy, and Psychology. Participants include older adults (60+) who can independently travel to the university.\n\nThe project is integrated into different subjects, in groups of 4-5 students, participants conduct a Comprehensive Geriatric Assessment (CGA), evaluating frailty using VIG-Frail, intrinsic capacity with ICOPE, quality of life with EUROQOL 5D-5L, and specific health indicators with Nursing Outcomes Classification (NOC).\n\nTo assess the program's effectiveness, several outcome measures will be analyzed including students' perceived knowledge, competencies, and skills, as well as older adults' awareness of their health status, lifestyle, and risk factors. Additionally, the satisfaction levels of both will be evaluated. The items will be evaluated using a 1-5 Likert Scale, and the analysis will be conducted with SPSS. Data recording will be carried out through REDCap.\n\nThe GEROS Project aligns with the United Nations' Sustainable Development Goals (SDGs), specifically SDG 3 (Good Health and Well-being) and SDG 10 (Reduced Inequalities). By offering care to the aging population and providing them with personalized health recommendations, the project promotes preventive strategies, active aging, and intergenerational learning.\n\nFurthermore, GEROS integrates innovative educational methodologies, encouraging experiential learning, collaboration with healthcare professionals, and the development of practical skills in real-world contexts. The program's scalability and adaptability could serve as a model for other universities and healthcare institutions aiming to enhance geriatric care through service-learning initiatives.",[500,501,502,30,503,504,505],"Frailty","Older People","Comprehensive Geriatric Assessment","SERVICE LEARNING","Students","Student Education","2025-03-19",{"date":508,"type":36},"2025-03-24",{"date":510,"type":36},"2024-11-11",{"date":512,"type":23},"2025-12-20",{"name":514,"class":43},"University of Vic - Central University of Catalonia",{"id":516,"slug":517,"hasResults":11,"nctId":518,"briefTitle":519,"officialTitle":520,"acronym":4,"eligibilityCriteria":521,"healthyVolunteers":17,"sex":52,"minAge":19,"maxAge":4,"enrollmentInfo":522,"targetDuration":4,"studyType":24,"phases":524,"briefSummary":525,"conditions":526,"keywords":529,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":534,"lastUpdatePostDateStruct":535,"startDateStruct":537,"completionDateStruct":539,"leadSponsor":541,"locationsCount":96},"100557117","blue-green-space-physical-activity-the-parco-del-mare-study-100557117","NCT06533943","Blue-green Space Physical Activity: the \"Parco Del Mare\" Study","Engaging in Physical Activity Carried Out in a Blue-green Space to Improve Health, Quality of Life and Physical Performance Among the Population: the \"Parco Del Mare\" Study Protocol","Inclusion Criteria:\n\n* Adult population aged \\>18 years old\n* Resident in Rimini\n\nExclusion Criteria:\n\n* Any alterations in communication skills and\u002For sensory functions so severe as to make it impossible to understand and\u002For execute the instructions given by the trainer (dementia, aphasia, blindness, deafness)",{"count":523,"type":23},30,[26],"This study protocol, describe the innovative study intervention which will be performed in a green-blue space in Italy in order to investigate on the improvements in wellbeing following participation in the study. This will be significant because it will provide evidence on the effectiveness of the supervised physical activities carried out in green-blue space in improving health, quality of life, physical performance, anthropometric outcomes and physiological parameters in adults, indicating the reasonableness for public health authorities to developing such activities.",[527,528,30],"Healthy Adults","Natural Outdoor Environment",[530,531,532,533],"blue-green space setting","physical activity intervention","outdoor exercise","public health","2024-12-09",{"date":536,"type":36},"2024-12-13",{"date":538,"type":36},"2022-02-01",{"date":540,"type":23},"2024-12-20",{"name":542,"class":43},"Università degli Studi 'G. d'Annunzio' Chieti e Pescara",{"id":544,"slug":545,"hasResults":11,"nctId":546,"briefTitle":547,"officialTitle":547,"acronym":548,"eligibilityCriteria":549,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":550,"targetDuration":4,"studyType":410,"phases":4,"briefSummary":551,"conditions":552,"keywords":555,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":559,"lastUpdatePostDateStruct":560,"startDateStruct":562,"completionDateStruct":564,"leadSponsor":566,"locationsCount":96},"100556702","evaluation-of-a-health-promotion-intervention-on-food-safety-in-women-during-pregnancy-100556702","NCT06528535","Evaluation of a Health Promotion Intervention on Food Safety in Women During Pregnancy","NPTM2","Inclusion Criteria:\n\n* Intervention group : Pregant women living in French Guiana during their pregancy and who benefited from the intervention\n* Control group : Pregant women living in French Guiana during their pregancy and who did not benefit from the intervention\n\nExclusion Criteria:\n\n* Refusal to participate to the study\n* No authorisation of participation from legal representatives for minor participants\n* Participants under guardianship or trusteeship",{"count":22,"type":23},"This is a comparative, observational study aiming to compare the diversity of the diet during pregnancy of women who have benefited from a health promotion intervention and who have not",[553,554,30],"Food Safety","Pregnancy Related",[556,557,558,184,175],"French Guiana","Pregnancy","Food safety","2024-07-31",{"date":561,"type":36},"2024-08-01",{"date":563,"type":36},"2023-09-22",{"date":565,"type":23},"2025-09",{"name":567,"class":43},"Centre Hospitalier de Cayenne",{"id":569,"slug":570,"hasResults":11,"nctId":571,"briefTitle":572,"officialTitle":573,"acronym":4,"eligibilityCriteria":574,"healthyVolunteers":17,"sex":52,"minAge":19,"maxAge":575,"enrollmentInfo":576,"targetDuration":4,"studyType":410,"phases":4,"briefSummary":578,"conditions":579,"keywords":581,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":587,"lastUpdatePostDateStruct":588,"startDateStruct":590,"completionDateStruct":592,"leadSponsor":594,"locationsCount":4},"100555616","comparative-study-of-empathy-and-anxiety-in-the-different-academic-years-at-the-beginning-of-academic-year-and-exam-period-in-healthy-students-100555616","NCT06514404","Comparative Study of Empathy and Anxiety in the Different Academic Years, at the Beginning of Academic Year and Exam Period in Healthy Students.","Comparative Study of Empathy and Anxiety in the Different Academic Years, at the Beginning of Academic Year and Exam Period and the Relationship of These Variables With Personality at the University of León and Madrid in the Degree of Nursing, Physiotherapy and Podiatry.","Inclusion Criteria:\n\n* Men and women who are studying a health grade.\n* Subjects that wish to participate in the study.\n\nExclusion Criteria:\n\n* Students who do not wish to participate in the study.","99 Years",{"count":577,"type":23},65,"Students from different health science degrees will carry out a study on the variables of empathy, anxiety and personality profile.",[173,30,580],"Health Behavior",[582,583,584,585,586],"health students","anxiety","empahty","assessment personality","Health behavior","2024-07-17",{"date":589,"type":36},"2024-07-23",{"date":591,"type":23},"2024-09-01",{"date":593,"type":23},"2024-09-10",{"name":595,"class":43},"Mayuben Private Clinic"]