[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100544058":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":23,"centralContacts":27,"locations":33,"responsibleParty":52,"collaborators":18,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":18,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":62,"minAge":63,"maxAge":18,"enrollmentInfo":64,"targetDuration":18,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":77,"overallStatus":36,"whyStopped":18,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},{"fullName":5,"class":6},"McGill University Health Centre\u002FResearch Institute of the McGill University Health Centre","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"SAFE program","EXPERIMENTAL","Participants will be asked to carry out the SAFE program with the help of a caregiver. Our healthcare professionals will visit them during the first week to explain to them and their caregivers how to perform the exercises correctly while using our website. All exercises will be performed using video capsules available on our website (https:\u002F\u002Fsafe-seniors.com\u002Ffr). The exercises are divided into 4 levels of difficulty: level 1 (light); level 2 (moderate); level 3 (moderate to vigorous); and level 4 (vigorous). Each level lasts 25 to 30 minutes and includes 5 exercise categories split into 5 videos: warm-up, strength, balance, flexibility, and endurance. The exercise intervention will include 3 sessions per week over 12 weeks.",[13],"Other: SAFE program (exercise intervention)",{"label":15,"type":16,"description":17,"interventionNames":18},"Control group","NO_INTERVENTION","Participants will be asked to continue their activities of daily living without making any changes.",null,[20],{"type":6,"name":21,"description":11,"armGroupLabels":22,"otherNames":18},"SAFE program (exercise intervention)",[9],[24],{"name":25,"affiliation":5,"role":26},"Jose Morais, MD","PRINCIPAL_INVESTIGATOR",[28],{"name":29,"role":30,"phone":31,"phoneExt":18,"email":32},"Guy Hajj Boutros","CONTACT","514-501-9975","guyelhajj@gmail.com",[34],{"facility":35,"status":36,"city":37,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"Royal Victoria Hospital - Glen site","RECRUITING","Montreal","Quebec","H4A 3J1","Canada","CA",{"type":43,"coordinates":44},"Point",[45,46],-73.58781,45.50884,{"lat":46,"lon":45},[49],{"name":29,"role":30,"phone":50,"phoneExt":51,"email":32},"514-8934-1934","35016",{"type":26,"investigatorFullName":53,"investigatorTitle":54,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"Jose Morais","Medical director","100544058","a-personalized-video-based-exercise-program-for-fall-prevention-in-frail-and-pre-frail-older-adult-100544058",false,"NCT06363942","A Personalized Video-based Exercise Program for Fall Prevention in Frail and Pre-frail Older Adult","Inclusion Criteria:\n\n* Considered Frail or Pre frail according to Fried's criteria\n\nExclusion Criteria:\n\n* Smoked within 6 months prior to study enrollment,\n* dementia diagnosos,\n* Abused drugs, medication or alcohol within up to 30 days prior to the start of the study.\n* drug or alcohol-addiction,\n* Heart disease, history of heart attacks or electrocardiogram abnormalities\n* Any family history of thrombosis, thrombosis risk,\n* hypocalcaemia,\n* uric acidemia,\n* orthostatic intolerance,\n* vestibular disorders,\n* considerable musculoskeletal issues,\n* chronic back pain,\n* head trauma,\n* seizures,\n* ulcers,\n* renal stones,\n* gastro-esophageal reflux disease,\n* renal function disorder,\n* hiatus hernia,\n* migraines,\n* mental illness diagnosis\n* prescribed medication that may interfere with the interpretation of the results",true,"ALL","70 Years",{"count":65,"type":66},100,"ESTIMATED","INTERVENTIONAL",[69],"NA","This is a randomized interventional clinical trial, whereby 100 participants will be randomized to either follow the SAFE exercise program (experimental group) or not (control group). At the end of the intervention, the experimental group will be encouraged to continue doing the exercises, and the control group will have the opportunity to participate in the SAFE exercises. 12 weeks post-intervention, the investigators will follow up with participants by telephone to follow up whether they are still following the SAFE program or not.",[72,73,74,75,76],"Fall Injury","Frailty","Old Age; Atrophy","Age-Related Atrophy","Age-Related Sarcopenia",[78,79,80,81],"frailty","exercise","older adult","ageing","2024-07-11",{"date":84,"type":85},"2024-07-12","ACTUAL",{"date":87,"type":85},"2024-07-01",{"date":89,"type":66},"2026-04-15",{"name":5,"class":6},1]