KCT0006270
Recruiting
未知
Establishment of comprehensive geriatric assessment based multidisciplinary teamapproach for hospitalized frail patients
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Symptoms, signs and abnormal clinical and laboratory findings, NEC
- Sponsor
- Seoul National University Bundang Hospital
- Enrollment
- 1040
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients 65 years of age or older who are hospitalized or scheduled to be hospitalized due to acute illness.
- •2\. Patients categorized to Frail or Prefrail assessed by Korean version of the Fatigue, Resilience, Ambulation, Illness and Loss of Weight scale (K\-FRAIL)
- •3\. Patients having two or more of the following diseases (hypertension, diabetes, ischemic heart disease, chronic lung disease, arthritis, stroke, depression, chronic kidney disease, dementia)
- •4\. Patient who are living at home for more than 3 months before hospitalisation.
- •5\. (For substudy 3 only) Patients who subject to conventional primary chemotherapy because local treatment for curative purposes (such as surgery, concurrent chemoradiotherapy, radiation therapy, etc.) is ineligible (stage stage 3 or higher)
- •6\. (For substudy 3 only) Patients confirmed histologically as cancer (gastric adenocarcinoma, colon adenocarcinoma, non\-small cell and small cell lung cancer, pancreatic adenocarcinoma, biliary adenocarcinoma)
Exclusion Criteria
- •1\. Patients who planned hospitalisation in the specialised care unit, such as an intensive care unit and/or acute stroke ward, at the time of admission
- •2\. Patients whose stage is terminal requiring hospice or palliative care.
- •3\. Life expectancy is less than 6 months
- •4\. Serious conditions that limit the participation in the research
- •5\. (For substudy 3 only) Patients who planned to use oral targeted therapy as a palliative first\-line chemotherapy
- •6\. (For substudy 3 only)) Patients who recur within 6 months after completion of adjuvant chemotherapy.
Outcomes
Primary Outcomes
Not specified
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