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Development of an Integrated Frailty Care Model for Older Adults

Development of an Integrated Frailty Care Model for Older Adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002983
Enrollment
40
Registered
2018-07-05
Start date
2018-06-07
Completion date
Unknown
Last updated
2019-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Behavioral : A. Usual care - 40 subjects from both groups(20 individuals from each intervention and control group) received usual care, which consist of CGA(comprehensive geriatric assessment) and med
of maximum heart rate, gradually increasing to 65&#37
) - Encourage people to work out as much as possible at home for more than 30 minutes every day. - Exercise therapy consists of aerobic exercise + strength exercise + balance training. ? At least tw

Sponsors

Ajou University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria

Exclusion criteria: - 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 ?

Design outcomes

Primary

MeasureTime frame
Improvement of frailty status;Change in the number of criteria of Fried’s frailty index

Secondary

MeasureTime frame
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)

Countries

Korea, Republic of

Contacts

Public ContactSooJeong Lee

Ajou University Hospital

rainbow.lsj.1004@gmail.com+82-31-219-5302

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026