{"type":"trials","record":{"id":21616,"source_id":"clinicaltrials-gov","external_id":"NCT07282951","title":"Strong Evidence: Digitally Delivered Exercise in Older Adults","brief_summary":"The investigators have successfully completed a pilot project focused on feasibility and user acceptability of a digitally delivered program for fall prevention in older adults. It was well received among a population of lower and moderate risk individuals. The investigators propose to extend this research by repeating the training program with the inclusion of a wait list control group. Group A (immediate intervention) will start their initial 12 week exercise program (Intensive Exercise) within 4 weeks of baseline (BL) measurement (as a cohort). This will be followed by an optional additional 12 week exercise program (Maintenance Exercise 2) that participants who complete at least 10 of the Exercise 1 classes will be invited to join. This will be followed by a 12 week wash out period. Measurements will occur each 12 weeks (BL, 12 week post randomization, 24 week post randomization, 36 week post randomization) Group B (waitlist control) will start with a 12 week life as normal period that is concurrent with Group A's intensive Exercise. They will start Intensive Exercise when Group A is doing Maintenance exercise. They will be invited to Maintenance Exercise while Group A is doing washout. They will not have a washout period. Measurements will occur at the same period(s) as Group A (i.e. all participants measured during the same time period). The intervention will be identical to what was offered in the past, and measurements will be very similar (removing those that did not show change with intervention or were deemed too difficult for participants).","overall_status":"Active Not Recruiting","phases":[],"study_type":"INTERVENTIONAL","sponsor":"University of California, San Diego","enrollment":60,"countries":["United States"],"start_date":"2025-12-01","completion_date":"2027-01-01","last_update_date":"2026-04-30","source_url":"https://clinicaltrials.gov/study/NCT07282951","editorial_summary":"A registered study indexed because it matched monitored longevity research terms. Registry status: Active Not Recruiting. Registration does not establish safety or effectiveness.","first_seen_at":"2026-09-24T01:17:08.26846+00:00","last_seen_at":"2026-09-25T06:10:07.378+00:00","metadata":{"sex":"ALL","acronym":null,"age_range":"60 Years","comparator":null,"organization":"University of California, San Diego","interventions":["Digitally Delivered Exercise"],"registry_source":"ClinicalTrials.gov","outcome_measures":["30 second chair stand — Baseline, 12 weeks, 24 weeks, 36 weeks","Grip Strength — Baseline, 12 weeks, 24 weeks, 36 weeks","Occipital to Wall Distance — BL, 12 weeks, 24 weeks, 36 weeks","Short Physical Performance Battery (SPPB) — Baseline, 12 weeks, 24 weeks, 36 weeks","The Timed Up and Go (TUG) — Baseline, 12 weeks, 24 weeks, 36 weeks","Body Muscle — Baseline, 12 weeks, 24 weeks, 36 weeks","Autophagy Flux — Baseline, 12 weeks, 24 weeks, 36 weeks"],"design_description":"RANDOMIZED · CROSSOVER · PREVENTION · DOUBLE","source_has_results":false},"controlled_terms":["Fall Prevention","Fall Prevention in Healthy Aging","Digitally Delivered Exercise"],"relevance_confidence":100,"source_quality_score":100,"freshness_score":100,"publication_state":"published","match_explanation":"Title contains controlled term: exercise.","quality_checked_at":"2026-09-25T06:10:20.034853+00:00","duplicate_cluster_key":"id:nct07282951","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2025-12-01 to 2027-01-01","comparator":null,"confidence":"structured-source","population":"ALL · 60 Years","provenance":{"duration":"start_date and completion_date","comparator":"registry arm fields","population":"registry eligibility fields","intervention":"registry intervention fields","participants":"enrollment","study_design":"study_type and registry design fields","evidence_stage":"phases","reported_outcome":"not available","outcomes_measured":"registry outcome-measure fields"},"generated_at":"2026-09-25T06:10:07.439Z","intervention":["Digitally Delivered Exercise"],"participants":60,"study_design":"RANDOMIZED · CROSSOVER · PREVENTION · DOUBLE","subject_scope":"Human clinical study registration","evidence_stage":"Phase not reported","safety_context":"Eligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians.","source_support":"Structured registry protocol metadata; no finding-level conclusion is generated.","main_limitation":"This is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.","reported_outcome":null,"outcomes_measured":["30 second chair stand — Baseline, 12 weeks, 24 weeks, 36 weeks","Grip Strength — Baseline, 12 weeks, 24 weeks, 36 weeks","Occipital to Wall Distance — BL, 12 weeks, 24 weeks, 36 weeks","Short Physical Performance Battery (SPPB) — Baseline, 12 weeks, 24 weeks, 36 weeks","The Timed Up and Go (TUG) — Baseline, 12 weeks, 24 weeks, 36 weeks","Body Muscle — Baseline, 12 weeks, 24 weeks, 36 weeks","Autophagy Flux — Baseline, 12 weeks, 24 weeks, 36 weeks"],"regulatory_context":"Trial registration is not regulatory approval and does not establish that an intervention is available."},"clinical_trial_topics":[{"topic_slug":"exercise","is_published":true,"match_reasons":["Title contains controlled term: exercise.","Abstract contains controlled term: exercise.","Source terminology contains: exercise.","Title supplies longevity context: older adult.","Study type is explicitly identified as INTERVENTIONAL."],"matched_fields":["title","abstract","controlled terminology","title context","study type"],"relevance_score":100,"intelligence_topics":{"name":"Exercise","slug":"exercise"}}],"content_sources":{"name":"ClinicalTrials.gov","homepage_url":"https://clinicaltrials.gov/"}},"canonical_url":"https://www.immortal.life/trials/21616","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}