{"type":"trials","record":{"id":22218,"source_id":"clinicaltrials-gov","external_id":"NCT07787663","title":"Promoting Autonomy Through ExerCisE (PACE) in Outpatient Geriatric Clinics","brief_summary":"Physical inactivity is highly prevalent among older adults and is associated with declines in physical function, independence, quality of life, and social participation. The PACE tool provides 35 tailored physical activity programs for frail, community-dwelling older adults. Programs are prescribed by healthcare professionals using simple clinical criteria and can be delivered remotely. Previous research has demonstrated the feasibility, acceptability, safety, and effectiveness of adapted physical activity programs. The main objective of the project is to implement PACE in the geriatric outpatient clinics (CEG) of the Institut Universitaire de Gériatrie de Montréal (IUGM) to prevent deconditioning, promote autonomy, and reduce the burden on caregivers and healthcare resources.","overall_status":"Completed","phases":[],"study_type":"INTERVENTIONAL","sponsor":"Université du Québec a Montréal","enrollment":162,"countries":["Canada"],"start_date":"2021-03-23","completion_date":"2025-09-11","last_update_date":"2026-08-26","source_url":"https://clinicaltrials.gov/study/NCT07787663","editorial_summary":"A registered study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.","first_seen_at":"2026-09-24T01:17:16.887272+00:00","last_seen_at":"2026-09-25T06:10:25.747+00:00","metadata":{"sex":"ALL","acronym":"PACE - OGC","age_range":"60 Years","comparator":"Control Group","organization":"Université du Québec a Montréal","interventions":["PACE"],"registry_source":"ClinicalTrials.gov","outcome_measures":["Feasibility of the PACE tool — 12 weeks","Adherence to the pace tool — 12 weeks","Usability of the PACE TOOL — 12 weeks","Acceptability of the PACE Tool — 12 weeks","Changes in objective physical measures — 12 weeks","Changes in caregiver burden after intervention — 12 weeks","Changes in the quality of life after intervention (12-Item Short Form Survey: SF-12) — 12 weeks"],"design_description":"RANDOMIZED · PARALLEL · TREATMENT · NONE","source_has_results":false},"controlled_terms":["Frailty","Sarcopenia","PACE"],"relevance_confidence":100,"source_quality_score":100,"freshness_score":100,"publication_state":"published","match_explanation":"Title contains controlled term: exercise.","quality_checked_at":"2026-09-25T06:10:37.875473+00:00","duplicate_cluster_key":"id:nct07787663","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2021-03-23 to 2025-09-11","comparator":"Control Group","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":"2026-09-25T06:10:25.758Z","intervention":["PACE"],"participants":162,"study_design":"RANDOMIZED · PARALLEL · TREATMENT · NONE","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":["Feasibility of the PACE tool — 12 weeks","Adherence to the pace tool — 12 weeks","Usability of the PACE TOOL — 12 weeks","Acceptability of the PACE Tool — 12 weeks","Changes in objective physical measures — 12 weeks","Changes in caregiver burden after intervention — 12 weeks","Changes in the quality of life after intervention (12-Item Short Form Survey: SF-12) — 12 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: physical activity.","Title supplies longevity context: geriatric.","Study type is explicitly identified as INTERVENTIONAL."],"matched_fields":["title","abstract","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/22218","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}