{"type":"trials","record":{"id":31410,"source_id":"clinicaltrials-gov","external_id":"NCT06633614","title":"PREhabilitation of Frail Elderly PAtients Undergoing majoR surgEry at HOME (PREPARE-HOME) Using Smart Wearables","brief_summary":"The goal of this clinical trial is to evaluate whether a prehabilitation program using wearable technology can improve physical function and postoperative outcomes in elderly patients (65 years or older) undergoing major elective non-cardiac surgery. The main questions it aims to answer are: Does the prehabilitation program improve physical function, as measured by the 6-minute walk test (6MWT), from baseline to pre-surgery? Does the prehabilitation program reduce postoperative complications and enhance recovery? Researchers will compare participants who receive the prehabilitation program with wearable technology (intervention group) to those receiving standard preoperative care (control group) to see if the intervention results in greater improvements in physical function and postoperative outcomes. Participants will: Follow a personalized exercise program monitored remotely via telemedicine. Wear a Fitbit Aspire 3 device to track vital signs such as heart rate and physical activity. Undergo assessments of physical function and quality of life before surgery.","overall_status":"Not Yet Recruiting","phases":[],"study_type":"INTERVENTIONAL","sponsor":"Singapore General Hospital","enrollment":190,"countries":[],"start_date":"2025-08-01","completion_date":"2028-01-31","last_update_date":"2025-05-15","source_url":"https://clinicaltrials.gov/study/NCT06633614","editorial_summary":"A registered study indexed because it matched monitored longevity research terms. Registry status: Not Yet Recruiting. Registration does not establish safety or effectiveness.","first_seen_at":"2026-09-25T01:16:21.317971+00:00","last_seen_at":"2026-09-25T06:10:07.378+00:00","metadata":{"sex":"ALL","acronym":"PREPARE@HOME","age_range":"65 Years","comparator":"Control","organization":"Singapore General Hospital","interventions":["Supervised prehabilitation programme"],"registry_source":"ClinicalTrials.gov","outcome_measures":["Change in Physical Function (6-Minute Walk Test) from baseline to before surgery. — baseline to 1-3 days pre-surgery.","Functional assessments — Baseline to 1-3 days before the surgery","Postoperative complications — Preoperative to up to 4 weeks after surgery.","Health Services outcomes — Preoperative to up to 8 weeks after surgery."],"design_description":"RANDOMIZED · PARALLEL · SUPPORTIVE CARE · NONE","source_has_results":false},"controlled_terms":["Frailty Syndrome","Supervised prehabilitation programme"],"relevance_confidence":100,"source_quality_score":100,"freshness_score":65,"publication_state":"published","match_explanation":"Title contains controlled term: wearable.","quality_checked_at":"2026-09-25T06:10:20.034853+00:00","duplicate_cluster_key":"id:nct06633614","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2025-08-01 to 2028-01-31","comparator":"Control","confidence":"structured-source","population":"ALL · 65 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":"2026-09-25T06:10:07.510Z","intervention":["Supervised prehabilitation programme"],"participants":190,"study_design":"RANDOMIZED · PARALLEL · SUPPORTIVE CARE · 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":["Change in Physical Function (6-Minute Walk Test) from baseline to before surgery. — baseline to 1-3 days pre-surgery.","Functional assessments — Baseline to 1-3 days before the surgery","Postoperative complications — Preoperative to up to 4 weeks after surgery.","Health Services outcomes — Preoperative to up to 8 weeks after surgery."],"regulatory_context":"Trial registration is not regulatory approval and does not establish that an intervention is available."},"clinical_trial_topics":[{"topic_slug":"digital-biomarkers","is_published":true,"match_reasons":["Title contains controlled term: wearable.","Abstract contains controlled term: wearable.","Title supplies longevity context: frail, elderly.","Study type is explicitly identified as INTERVENTIONAL."],"matched_fields":["title","abstract","title context","study type"],"relevance_score":100,"intelligence_topics":{"name":"Digital biomarkers","slug":"digital-biomarkers"}}],"content_sources":{"name":"ClinicalTrials.gov","homepage_url":"https://clinicaltrials.gov/"}},"canonical_url":"https://www.immortal.life/trials/31410","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}