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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05731167
Other study ID # 202112187RIND
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 7, 2023
Est. completion date July 31, 2025

Study information

Verified date February 2023
Source National Taiwan University Hospital
Contact Kun-Pei Lin, MD
Phone +886223123456
Email dtmed512@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

We aim to (1) use a multifaceted, frailty assessment model. (2) use randomized controlled trials to deal with and intervene with cross-field, multi-faceted and intelligent remote management strategies for the elderly with different degrees of frailty, to further observe functional changes and analyze the probability of adverse prognosis such as falls, hospitalization, and death in the future


Description:

Background: Frailty is a common problem among the elderly, and it is closely related to their own age, chronic diseases, physical function, and nutritional status. The higher the incidence, the higher the age. Frailty is also associated with many adverse outcomes, such as falls, disability and even mortality. At present, there is no ideal treatment for frailty. It is best to start with prevention and take precautions against various frailty factors in advance. There are two types of frailty assessments in this study. The Clinical Frailty Scale is a single observational assessment method, which can roughly know your frailty degree. Frailty indicators are further combined with questionnaires and instrumental measurements, which can be subdivided to explore different weaknesses such as subjective frailty, objective frailty, sarcopenia, osteoporosis risk, and fall risk for analysis. Objects: Elderly people in the community (over 65 years old) who seek medical treatment in the Geriatrics Department of National Taiwan University Hospital, and who are willing to accept the frailty index test are eligible for admission. We expect to enroll about 216 cases from 2023.2.1 to 2024.12.31 with intervene and follow up for 1 year. Method:. All the elders were given questionnaires and instruments to measure various frailty indicators, such as walking speed, standing up and walking test, muscle mass index, grip strength, 5 times of sitting and standing speed, and various physiological indicators such as blood oxygen, body fat, etc. The subjects will be randomly assigned to the intervention group or the control group. The control group will receive routine outpatient care. The intervention group will receive multi-faceted frailty prevention and treatment programs such as physical exercises, nutritional advice, cognitive training, and drug education. After that, the prognosis will be tracked by telephone every 3 months, and the self-evaluation questionnaire and the measurement of frailty indicators will be carried out at the 6th and 12th months. In order to observe the changes in the prognosis and frailty indicators of the two groups in one year.


Recruitment information / eligibility

Status Recruiting
Enrollment 216
Est. completion date July 31, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - adults aged greater than 65 years in outpatient department Exclusion Criteria: - with dementia - with active cancer and those unable to operate or follow measuring instructions. - Individuals with pacemakers or metal implants were excluded because those devices may interfere with measurement of body composition using the bioelectrical impedance analysis (BIA) technique

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Multidomain frailty prevention method
We use the nutrition, physical training, medication consultation, cognition training to prevent the occurrence of frailty or other adverse outcome.
Other:
Regular follow up
Subjects will receive regular follow up and suggestion in outpatient department.

Locations

Country Name City State
Taiwan Kun-Pei Lin Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fall fall rate will be evaluated by phone contact to subjects. 1 year
Primary Emergency room visits Emergency room visits will be evaluated by phone contact to subjects. 1 year
Primary Hospitalization Hospitalization times will be evaluated by phone contact to subjects. 1 year
Secondary Skeletal muscle index Skeletal muscle index will be measured by Bioelectrical impedance analysis. 1 year
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