{"type":"trials","record":{"id":35212,"source_id":"clinicaltrials-gov","external_id":"NCT07085000","title":"Cognitive and Physical Frailty as Predictors of Decision Satisfaction in Geriatric Gynecologic Oncology","brief_summary":"This prospective observational study aims to evaluate the association between preoperative cognitive function, measured by the Montreal Cognitive Assessment (MoCA), and physical frailty, assessed using the Clinical Frailty Scale (CFS), with postoperative decision satisfaction and adaptation in geriatric patients undergoing gynecologic cancer surgery. Approximately 60 to 70 female patients aged 65 years or older will be enrolled. Participants will complete preoperative assessments of cognitive status and frailty. Postoperative outcomes including decision satisfaction, medication adherence, mobilization, respiratory exercise compliance, and return to functional baseline will be evaluated. The study is conducted at İzmir City Hospital and is designed to generate preliminary data to inform larger-scale research.","overall_status":"Completed","phases":[],"study_type":"OBSERVATIONAL","sponsor":"Izmir City Hospital","enrollment":68,"countries":["Turkey (Türkiye)"],"start_date":"2025-05-10","completion_date":"2025-08-15","last_update_date":"2025-08-17","source_url":"https://clinicaltrials.gov/study/NCT07085000","editorial_summary":"A registered study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.","first_seen_at":"2026-09-25T01:20:20.087268+00:00","last_seen_at":"2026-09-25T06:10:07.378+00:00","metadata":{"sex":"FEMALE","acronym":"GYNCOGFRAIL","age_range":"65 Years","comparator":null,"organization":"Izmir City Hospital","interventions":["No Intervention - Observational Assessment"],"registry_source":"ClinicalTrials.gov","outcome_measures":["Postoperative Decision Satisfaction Score — From the day of surgery to postoperative day 15.","Preoperative Cognitive Function (MoCA) — Up to 1 day before surgery","Preoperative Physical Frailty (CFS) — Up to 1 day before surgery","Postoperative Adaptation Score — From the day of surgery to 30 days after surgery","Length of Hospital Stay — From date of surgery until hospital discharge, assessed up to 14 days","30-Day Postoperative Complications — Within 30 days after surgery"],"design_description":null,"source_has_results":false},"controlled_terms":["Gynecologic Cancer","Frailty","Cognitive Impairment","Geriatric Oncology","No Intervention - Observational Assessment"],"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:nct07085000","duplicate_of_id":null,"evidence_snapshot":{"status":"structured","version":1,"duration":"2025-05-10 to 2025-08-15","comparator":null,"confidence":"structured-source","population":"FEMALE · 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":"2026-09-25T06:10:07.491Z","intervention":["No Intervention - Observational Assessment"],"participants":68,"study_design":"OBSERVATIONAL","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":["Postoperative Decision Satisfaction Score — From the day of surgery to postoperative day 15.","Preoperative Cognitive Function (MoCA) — Up to 1 day before surgery","Preoperative Physical Frailty (CFS) — Up to 1 day before surgery","Postoperative Adaptation Score — From the day of surgery to 30 days after surgery","Length of Hospital Stay — From date of surgery until hospital discharge, assessed up to 14 days","30-Day Postoperative Complications — Within 30 days after surgery"],"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 OBSERVATIONAL."],"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/35212","automation_disclosure":"Generated automatically from cited source metadata. No scientist, clinician, researcher, editor, or human reviewer evaluates this publication before release."}