{"type":"trials","record":{"id":35510,"source_id":"clinicaltrials-gov","external_id":"NCT06536985","title":"Effect of an Oral Frailty Measures Intervention Programs in Institutionalized Elders","brief_summary":"This is a compelling 16-week prospective, double-blind, whole-cluster randomized controlled trial(RCT).This study will recruit 226 older adults over the age of 65.Based on King's goal attainment theory, a program to promote oral health is developed.The study aims to evaluate the effectiveness of a mixed face-to-face and eHealth oral health promotion program for older adults with oral frailty in nursing homes, based on the Theory of Planned Behavior.","overall_status":"Not Yet Recruiting","phases":[],"study_type":"INTERVENTIONAL","sponsor":"Hangzhou Normal University","enrollment":226,"countries":["China"],"start_date":"2024-11-11","completion_date":"2025-11-11","last_update_date":"2024-11-04","source_url":"https://clinicaltrials.gov/study/NCT06536985","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":"2026-09-25T01:20:20.087268+00:00","last_seen_at":"2026-09-25T06:25:08.953+00:00","metadata":{"sex":"ALL","acronym":null,"age_range":"65 Years","comparator":"Contral group","organization":"Hangzhou Normal University","interventions":["treatment group","Contral group"],"registry_source":"ClinicalTrials.gov","outcome_measures":["Assessing changes in the risk of oral frailty — Before and 16 weeks after the intervention","Assessing changes in oral function status — Before and 16 weeks after the intervention","Assessment of changes in body composition — Before and 16 weeks after the intervention","Nutrition Screening — Before and 16 weeks after the intervention","Changes in Social Support — Before and 16 weeks after the intervention","Self Efficacy — Before and 16 weeks after the intervention","Changes in frailty — Before and 16 weeks after the intervention"],"design_description":"RANDOMIZED · PARALLEL · TREATMENT · DOUBLE","source_has_results":false},"controlled_terms":["Frailty","treatment group","Contral group"],"relevance_confidence":100,"source_quality_score":100,"freshness_score":65,"publication_state":"published","match_explanation":"Title contains controlled term: frailty.","quality_checked_at":"2026-09-25T06:25:14.10514+00:00","duplicate_cluster_key":"id:nct06536985","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2024-11-11 to 2025-11-11","comparator":"Contral 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":"2026-09-25T06:25:09.006Z","intervention":["treatment group","Contral group"],"participants":226,"study_design":"RANDOMIZED · PARALLEL · TREATMENT · 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":["Assessing changes in the risk of oral frailty — Before and 16 weeks after the intervention","Assessing changes in oral function status — Before and 16 weeks after the intervention","Assessment of changes in body composition — Before and 16 weeks after the intervention","Nutrition Screening — Before and 16 weeks after the intervention","Changes in Social Support — Before and 16 weeks after the intervention","Self Efficacy — Before and 16 weeks after the intervention","Changes in frailty — Before and 16 weeks after the intervention"],"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/35510","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}