Development of an Integrated Frailty Care Model for Older Adults
- Conditions
- Not Applicable
- Registration Number
- KCT0002983
- Lead Sponsor
- Ajou University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Active, not recruiting
- Sex
- All
- Target Recruitment
- 40
Participants should be able to participate in the trial consistently for 4 months, meeting the following criteria.
- 70 years or older
- Those visiting outpatient clinics or hospitalized
- Pre-frail or frail status determined by one or more categories of the K-Frail scale and one or more categories of the Fried’s phenotype criteria
- A person who has given written informed consent to conducting research
- Person in a vulnerable situation as defined by Article 30, Section 1 of the Pharmaceutical Act
- Medically identified dementia, Alzheimer’s disease, depression, bipolar disorder, or schizophrenia patients
- Patients with incident systemic arrhythmia thrombosis, myocardial infarction, coronary artery bypass graft surgery, or percutaneous coronary intervention within three months of screening
- Unstable angina patients with symptoms
- Patients identified as heart failure, classified as New York Heart Association Class III and IV
- Severe pulmonary hypertension uncontrolled with medication
- In case of chest pain, severe breathing difficulties or other safety problems detected during screening or evaluation
- Severe haemostatic disorder with platelets less than 75,000 ?
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement of frailty status;Change in the number of criteria of Fried’s frailty index
- Secondary Outcome Measures
Name Time Method Muscle mass;SPPB(Short Physical Performance Battery);MMSE(Mini-Mental State Examination);GDS(Geriatric Depression Scale);Other clinical indicators (CBC, total cholesterol, albumin, 25- OH-vitamin D)