{"type":"trials","record":{"id":28427,"source_id":"clinicaltrials-gov","external_id":"NCT07733726","title":"Oral Motor and Cognitive Dual-Task Training (OMCDT) Program for Improving Oral and Cognitive Functions Among People With Oral Frailty","brief_summary":"The goal of this clinical trial is to proposes a novel Oral Motor and Cognitive Dual-Task Training (OMCDT) program that combines both oral motor exercises and cognitive tasks to improve brain and oral function at the same time. It will also learn about the safety of drug ABC. The main questions it aims to answer is: Does the OMCDT training can improve the oral and cognitive functions? Participants will: Take the OMCDT training once a week for 32 weeks Visit the lab twice in the intervention period (16-week, 32-week) for checkups and tests","overall_status":"Enrolling By Invitation","phases":[],"study_type":"INTERVENTIONAL","sponsor":"The Hong Kong Polytechnic University","enrollment":66,"countries":["Hong Kong"],"start_date":"2026-05-01","completion_date":"2027-06-15","last_update_date":"2026-07-29","source_url":"https://clinicaltrials.gov/study/NCT07733726","editorial_summary":"A registered study indexed because it matched monitored longevity research terms. Registry status: Enrolling By Invitation. Registration does not establish safety or effectiveness.","first_seen_at":"2026-09-25T00:17:13.911889+00:00","last_seen_at":"2026-09-25T06:25:08.953+00:00","metadata":{"sex":"ALL","acronym":"OMCDT","age_range":"50 Years","comparator":"Control Group","organization":"The Hong Kong Polytechnic University","interventions":["Oral Motor and Cognitive Dual-Task Training (OMCDT)","Oral motor exercise"],"registry_source":"ClinicalTrials.gov","outcome_measures":["Proportion of participant randomized divided by proportion of people eligible — Week 16; Week-32","Number of participants that withdraw divided by number of participants randomized — 16-week; 32-week","Proportion of participants who complete the allocated intervention with a minimum of 80% attendance — 16-week; 32-week","Maximum tongue pressure — Baseline, 16-week, 32-week","Oral motor coordination — baseline; 16-week; 32-week","Masticatory ability — baseline; 16-week; 32-week","Self-reported oral health — Baseline, 16-week, 32-week","Global cognitive status — Baseline, 16-week, 32-week","Executive function — baseline; 16-week; 32-week","Memory — baseline; 16-week; 32-week"],"design_description":"RANDOMIZED · PARALLEL · TREATMENT · SINGLE","source_has_results":false},"controlled_terms":["Oral Frailty","Mild Cognitive Impairment (MCI)","Moderate Cognitive Impairment","Oral Motor and Cognitive Dual-Task Training (OMCDT)","Oral motor exercise"],"relevance_confidence":100,"source_quality_score":100,"freshness_score":100,"publication_state":"published","match_explanation":"Title contains controlled term: frailty.","quality_checked_at":"2026-09-25T06:25:14.10514+00:00","duplicate_cluster_key":"id:nct07733726","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2026-05-01 to 2027-06-15","comparator":"Control Group","confidence":"structured-source","population":"ALL · 50 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":"2026-09-25T06:25:08.962Z","intervention":["Oral Motor and Cognitive Dual-Task Training (OMCDT)","Oral motor exercise"],"participants":66,"study_design":"RANDOMIZED · PARALLEL · TREATMENT · SINGLE","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":["Proportion of participant randomized divided by proportion of people eligible — Week 16; Week-32","Number of participants that withdraw divided by number of participants randomized — 16-week; 32-week","Proportion of participants who complete the allocated intervention with a minimum of 80% attendance — 16-week; 32-week","Maximum tongue pressure — Baseline, 16-week, 32-week","Oral motor coordination — baseline; 16-week; 32-week","Masticatory ability — baseline; 16-week; 32-week","Self-reported oral health — Baseline, 16-week, 32-week","Global cognitive status — Baseline, 16-week, 32-week","Executive function — baseline; 16-week; 32-week","Memory — baseline; 16-week; 32-week"],"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.","Source terminology contains: frailty.","Title supplies longevity context: frailty, frail.","Study type is explicitly identified as INTERVENTIONAL."],"matched_fields":["title","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/28427","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}