[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100640034":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":30,"centralContacts":38,"locations":48,"responsibleParty":65,"collaborators":17,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":74,"eligibilityCriteria":75,"healthyVolunteers":76,"sex":77,"minAge":78,"maxAge":17,"enrollmentInfo":79,"targetDuration":17,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":92,"overallStatus":50,"whyStopped":17,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":107},{"fullName":5,"class":6},"Sheba Medical Center","OTHER_GOV",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"intervention group","EXPERIMENTAL","a comprehensive assessment result report, which is divided into major areas of health: cardiovascular, lifestyle habits, mental health, cognitive function, sensory health, sleep patterns, metabolic health, physical strength (stamina), women's and men's health, and biological aging; a personalized recommendation program will be tailored to the participant's assessment results.",[13],"Other: healthspan personalized protocol",{"label":15,"type":16,"description":17,"interventionNames":18},"control group","SHAM_COMPARATOR",null,[19],"Other: Control",[21,26],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":17},"OTHER","healthspan personalized protocol","The study will include an extensive aging assessment and imaging protocol (baseline assessment), including comprehensive physical, functional, sensory, cognitive, and mental assessment. Each participant in the intervention group will receive a personalized intervention program based on an integrative systems approach analysis. In addition, a uniquely developed application will track compliance and monitor physiological data through a provided wearable device. Each participant will visit the center aging after 6 months for a blood test and after 12 months for a second extensive diagnostic protocol, similar to the baseline assessment protocol.",[9],{"type":22,"name":27,"description":28,"armGroupLabels":29,"otherNames":17},"Control","The control group will be assessed at baseline without receiving an intervention program. Each participant will visit the center aging after 6 months for a blood test and after 12 months for a second extensive diagnostic protocol, similar to the baseline assessment protocol.",[15],[31,34,36],{"name":32,"affiliation":5,"role":33},"Evelyne Bischof, MD PhD","PRINCIPAL_INVESTIGATOR",{"name":35,"affiliation":5,"role":33},"Abigail Goshen, PhD",{"name":37,"affiliation":5,"role":33},"Tzipi Strauss, MD",[39,44],{"name":40,"role":41,"phone":42,"phoneExt":17,"email":43},"tzipi strauss, MD","CONTACT","972526664446","zipora.strauss@sheba.heath.gov.il",{"name":45,"role":41,"phone":46,"phoneExt":17,"email":47},"evelyne bischof, MD PhD","972512504301","bischofevelyne@gmail.com",[49],{"facility":5,"status":50,"city":51,"state":52,"zip":53,"country":54,"countryCode":55,"cosmosGeoPoint":56,"geoPoint":61,"contacts":62},"RECRUITING","Ramat Gan","Tel Aviv","5220001","Israel","IL",{"type":57,"coordinates":58},"Point",[59,60],34.81065,32.08227,{"lat":60,"lon":59},[63],{"name":32,"role":41,"phone":64,"phoneExt":17,"email":47},"00972512504301",{"type":33,"investigatorFullName":66,"investigatorTitle":67,"investigatorAffiliation":5,"oldNameTitle":17,"oldOrganization":17},"Tzipi Strauss, MD MSc","PI","100640034","sheba-healthspan-research-population-sharp-trial---sheba-longevity-center-diagnostic-and-intervention-protocol-to-lower-biological-age-in-older-adults-100640034",false,"NCT07596576","Sheba Healthspan Research Population (SHARP) Trial - Sheba Longevity Center Diagnostic and Intervention Protocol to Lower Biological Age in Older Adults","Sheba Healthspan Research Population (SHARP) Trial","SHARP","Inclusion Criteria:\n\n* Healthy older adults \\>50 years old men and women\n\nExclusion Criteria:\n\n1. A former diagnostic of a significant cognitive reduction (MoCa score \\\u003C 24 ).\n2. Former diagnosis of neurodegenerative disease as Alzheimer's disease, Parkinson's disease, Lewy body dementia.\n3. Former diagnosis of psychiatric disease.\n4. In the past two years, underwent chemotherapy or radiation therapy.",true,"ALL","50 Years",{"count":80,"type":81},1500,"ESTIMATED","INTERVENTIONAL",[84],"NA","Background: Population aging is accelerating rapidly in Israel and worldwide, necessitating adaptation of the healthcare system and considering new approaches that serve the needs of older adult populations.\n\nWorking hypothesis and aims: We hypothesize that a personalized health and behavior intervention program will decrease the biological age as assessed by several biological aging clocks and improve functional and cognitive performance among older adults.\n\nMethods: We propose to conduct a randomized study among healthy community-dwelling elderly subjects (\\>50 years old). The study will include an extensive aging assessment and imaging protocol (baseline assessment), including comprehensive physical, functional, sensory, cognitive, and mental assessment. Each participant in the intervention group will receive a personalized intervention program based on an integrative systems approach analysis. In addition, a uniquely developed application will track compliance and monitor physiological data through a provided wearable device. The control group will be assessed at baseline without receiving an intervention program. Each participant will visit the center aging after 6 months for a blood test and after 12 months for a second extensive diagnostic protocol, similar to the baseline assessment protocol. About 1,500 subjects will be recruited to participate in the study.\n\nExpected results: Obtaining data at two points will allow us to examine efficiency and compliance with a personalized intervention program based on integrative systems analysis models. We expect biological age, general well-being, and various clinical and psychosocial outcomes in the intervention group will decrease and improve compared to the control group.\n\nStudy importance and relevance: The obtained results may help establish evidence-based healthy aging diagnostics protocols and an effective personalized intervention program that might be applied, with proper modifications, to national healthcare organizations for the general older adult population. In addition, to provides a scientific basis on which policymakers and intervention programs can rely to develop national guidelines for promoting extended health.",[87,88,89,90,91],"Healthy Aging","Healthspan","Biological Age","Intrinsic Capacity","Immunaging",[93,94,95,96,97],"healthy longevity","healthspan","geromedicine","biological age","health trajectories","2026-05-18",{"date":100,"type":101},"2026-05-19","ACTUAL",{"date":103,"type":101},"2024-03-01",{"date":105,"type":81},"2027-12-01",{"name":5,"class":6},1]