{"type":"trials","record":{"id":30150,"source_id":"clinicaltrials-gov","external_id":"NCT07634406","title":"Nurse-Led Telehealth Frailty Management in Older Adults","brief_summary":"Frailty is an important geriatric syndrome associated with reduced physiological reserve, functional decline, falls, hospitalization, and increased health care use among older adults. This randomized controlled trial aims to evaluate the effect of a nurse-led telehealth-supported multicomponent frailty management program on frailty level and functional status in older adults living at home. The study will be conducted as a single-center, two-arm, parallel-group randomized controlled trial. A total of 100 older adults aged 65 years and older who are living at home and are frail or at risk of frailty will be randomly assigned to either the intervention group or the control group in a 1:1 ratio. Participants in the intervention group will receive an 6-week nurse-led telehealth-supported frailty management program, including weekly telephone counseling and individualized follow-up. Participants in the control group will continue usual care. Data will be collected at baseline, at 6 weeks, and at 18 weeks. The primary outcome is frailty level measured using the FRAIL Scale. Secondary outcomes include functional status, depressive symptoms, number of falls, emergency department visits, and hospitalizations.","overall_status":"Recruiting","phases":[],"study_type":"INTERVENTIONAL","sponsor":"Kutahya Health Sciences University","enrollment":100,"countries":["Turkey (Türkiye)"],"start_date":"2026-06-05","completion_date":"2026-10-15","last_update_date":"2026-07-27","source_url":"https://clinicaltrials.gov/study/NCT07634406","editorial_summary":"A registered study indexed because it matched monitored longevity research terms. Registry status: Recruiting. Registration does not establish safety or effectiveness.","first_seen_at":"2026-09-25T01:16:16.485702+00:00","last_seen_at":"2026-09-25T06:10:07.378+00:00","metadata":{"sex":"ALL","acronym":null,"age_range":"65 Years","comparator":"Usual Care","organization":"Kutahya Health Sciences University","interventions":["Nurse-Led Telehealth-Supported Multicomponent Frailty Management Program"],"registry_source":"ClinicalTrials.gov","outcome_measures":["Frailty Level Assessed by the FRAIL Scale — Baseline, 6 weeks, and 18 weeks","Functional Status Assessed by the Lawton-Brody Instrumental Activities of Daily Living Scale — Baseline, 6 weeks, and 1…","Depressive Symptoms Assessed by the 15-Item Geriatric Depression Scale — Baseline, 6 weeks, and 18 weeks","Number of Falls During the Study Period — From baseline to 18 weeks","Number of Emergency Department Visits During the Study Period — From baseline to 18 weeks","Number of Hospitalizations During the Study Period — From baseline to 18 weeks"],"design_description":"RANDOMIZED · PARALLEL · SUPPORTIVE CARE · NONE","source_has_results":false},"controlled_terms":["Frailty","Nurse-Led Telehealth-Supported Multicomponent Frailty Management Program"],"relevance_confidence":100,"source_quality_score":100,"freshness_score":100,"publication_state":"published","match_explanation":"Title contains controlled term: frailty.","quality_checked_at":"2026-09-25T06:10:20.034853+00:00","duplicate_cluster_key":"id:nct07634406","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2026-06-05 to 2026-10-15","comparator":"Usual Care","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":"2026-09-25T06:10:07.405Z","intervention":["Nurse-Led Telehealth-Supported Multicomponent Frailty Management Program"],"participants":100,"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":["Frailty Level Assessed by the FRAIL Scale — Baseline, 6 weeks, and 18 weeks","Functional Status Assessed by the Lawton-Brody Instrumental Activities of Daily Living Scale — Baseline, 6 weeks, and 1…","Depressive Symptoms Assessed by the 15-Item Geriatric Depression Scale — Baseline, 6 weeks, and 18 weeks","Number of Falls During the Study Period — From baseline to 18 weeks","Number of Emergency Department Visits During the Study Period — From baseline to 18 weeks","Number of Hospitalizations During the Study Period — From baseline to 18 weeks"],"regulatory_context":"Trial registration is not regulatory approval and does not establish that an intervention is available."},"clinical_trial_topics":[{"topic_slug":"frailty","is_published":true,"match_reasons":["Title contains controlled term: frailty.","Abstract contains controlled term: frailty.","Source terminology contains: frailty.","Title supplies longevity context: frailty, frail.","Study type is explicitly identified as INTERVENTIONAL."],"matched_fields":["title","abstract","controlled terminology","title context","study type"],"relevance_score":100,"intelligence_topics":{"name":"Frailty","slug":"frailty"}}],"content_sources":{"name":"ClinicalTrials.gov","homepage_url":"https://clinicaltrials.gov/"}},"canonical_url":"https://www.immortal.life/trials/30150","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}