{"type":"trials","record":{"id":31437,"source_id":"clinicaltrials-gov","external_id":"NCT06875024","title":"The Effects of Intelligent Intervention Programs on Hospitalized Elderly People With Frailty.","brief_summary":"Background: As the aging population grows, hospitalized elderly individuals with frailty have become a major concern. Frailty is a complex syndrome linked to aging, marked by dependency and vulnerability. Elderly patients often face chronic diseases, making them more susceptible to frailty. Studies show frailty prevalence in hospitalized elderly patients is 88.7%, and 75.3% among kidney disease patients. Frailty is associated with advanced age, female gender, low body mass index, comorbidities, and poor nutrition, increasing the risks of falls, hospitalization, and mortality. Frail kidney disease patients face worse outcomes. However, frailty is reversible with early intervention. Current treatments, based on comprehensive geriatric assessment (CGA), require significant resources. This study aims to explore frailty prevention and care through research and intervention development. Purpose: To explore the effectiveness of an intelligent intervention program in improving frailty among hospitalized elderly individuals. Methods: An experimental research design was adopted. A total of 156 hospitalized elderly patients with kidney disease who met the inclusion criteria were recruited through convenience sampling. Participants were randomly assigned to either the experimental group (n = 78) or the control group (n = 78). The experimental group received a 12-week intelligent intervention program, while the control group received routine care.Subsequently, data on frailty level, daily living function 30 days after discharge, and unexpected readmission rate 30 days after discharge will be collected by researchers and analyzed using SPSS 22.0, including chi-square tests, repeated measures ANOVA, and Generalized Estimating Equations (GEE) for intra-group and inter-group comparisons of each outcome variable. Expected research results: This study aims to understand the current status and influencing factors of frailty among hospitalized elderly patients with kidney disease and to develop an intelligent intervention program. The goal is to provide clinical nursing staff with a frailty care strategy for hospitalized patients, effectively reducing frailty among elderly inpatients, improving their daily functional ability after discharge, and decreasing hospital readmission rates. Condition or disease: frailty Intervention/treatment: intelligent intervention program","overall_status":"Not Yet Recruiting","phases":[],"study_type":"INTERVENTIONAL","sponsor":"National Taipei University of Nursing and Health Sciences","enrollment":156,"countries":["Taiwan"],"start_date":"2025-04-15","completion_date":"2026-12-31","last_update_date":"2025-04-03","source_url":"https://clinicaltrials.gov/study/NCT06875024","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":null,"age_range":"65 Years","comparator":"Control group","organization":"National Taipei University of Nursing and Health Sciences","interventions":["Intelligent intervention programs"],"registry_source":"ClinicalTrials.gov","outcome_measures":["Fried frailty phenotype — pre-intervention, baseline (T0)","Fried frailty phenotype — 4 weeks after intervention, discharge(T1)","Fried frailty phenotype — 8 weeks after intervention(T2)","Fried frailty phenotype — 12 weeks after intervention(T3)","physical activity function- Activities of daily living(ADL) — pre-intervention, baseline (T0)","physical activity function- Activities of daily living(ADL) — 4 weeks after intervention, discharge(T1)","physical activity function- Activities of daily living(ADL) — 8 weeks after intervention(T2)","physical activity function- Activities of daily living(ADL) — 12 weeks after intervention(T3)","physical activity function-Chair Stand Test — pre-intervention, baseline (T0)","physical activity function-Chair Stand Test — 4 weeks after intervention, discharge(T1)","physical activity function-Chair Stand Test — 8 Weeks after intervention(T2)","physical activity function-Chair Stand Test — 12 Weeks after intervention(T3)","15-item geriatric depression scale(GDS-15) — pre-intervention, baseline (T0)","15-item geriatric depression scale(GDS-15) — 4 weeks after intervention, discharge(T1)","15-item geriatric depression scale(GDS-15) — 8 Weeks after intervention(T2)","15-item geriatric depression scale(GDS-15) — 12 Weeks after intervention(T3)","the Chinese version of the Pittsburgh Sleep Quality Index(CPSQI) — pre-intervention, baseline (T0)","the Chinese version of the Pittsburgh Sleep Quality Index(CPSQI) — 4 weeks after intervention, discharge(T1)","the Chinese version of the Pittsburgh Sleep Quality Index(CPSQI) — 8 Weeks after intervention(T2)","the Chinese version of the Pittsburgh Sleep Quality Index(CPSQI) — 12 Weeks after intervention(T3)"],"design_description":"RANDOMIZED · PARALLEL · HEALTH SERVICES RESEARCH · DOUBLE","source_has_results":false},"controlled_terms":["Frailty in Older Adults","Intelligent intervention programs"],"relevance_confidence":100,"source_quality_score":100,"freshness_score":65,"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:nct06875024","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2025-04-15 to 2026-12-31","comparator":"Control group","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":"2026-09-25T06:10:07.516Z","intervention":["Intelligent intervention programs"],"participants":156,"study_design":"RANDOMIZED · PARALLEL · HEALTH SERVICES RESEARCH · 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":["Fried frailty phenotype — pre-intervention, baseline (T0)","Fried frailty phenotype — 4 weeks after intervention, discharge(T1)","Fried frailty phenotype — 8 weeks after intervention(T2)","Fried frailty phenotype — 12 weeks after intervention(T3)","physical activity function- Activities of daily living(ADL) — pre-intervention, baseline (T0)","physical activity function- Activities of daily living(ADL) — 4 weeks after intervention, discharge(T1)","physical activity function- Activities of daily living(ADL) — 8 weeks after intervention(T2)","physical activity function- Activities of daily living(ADL) — 12 weeks after intervention(T3)","physical activity function-Chair Stand Test — pre-intervention, baseline (T0)","physical activity function-Chair Stand Test — 4 weeks after intervention, discharge(T1)","physical activity function-Chair Stand Test — 8 Weeks after intervention(T2)","physical activity function-Chair Stand Test — 12 Weeks after intervention(T3)","15-item geriatric depression scale(GDS-15) — pre-intervention, baseline (T0)","15-item geriatric depression scale(GDS-15) — 4 weeks after intervention, discharge(T1)","15-item geriatric depression scale(GDS-15) — 8 Weeks after intervention(T2)","15-item geriatric depression scale(GDS-15) — 12 Weeks after intervention(T3)","the Chinese version of the Pittsburgh Sleep Quality Index(CPSQI) — pre-intervention, baseline (T0)","the Chinese version of the Pittsburgh Sleep Quality Index(CPSQI) — 4 weeks after intervention, discharge(T1)","the Chinese version of the Pittsburgh Sleep Quality Index(CPSQI) — 8 Weeks after intervention(T2)","the Chinese version of the Pittsburgh Sleep Quality Index(CPSQI) — 12 Weeks after intervention(T3)"],"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/31437","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}