- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04139837
Frailty in Daily Practice: Screening, Consultation and Education Activities
The present study is designed to to estimate the prevalence of frailty and pre-frailty and their associated factors in community-dwelling populations aged 50 years and above in Hong Kong, and to explore the views of participants taking part in a community health talks or activities on frailty about what the participants felt or had gained from participating, concerns, and suggestions for change or improvement.
A survey of 15000 people aged 50 years or older identified in community facilities will be conducted. The participants will be invited to their affiliated centres for a brief screening using the FRAIL scale and assessment. A series of community health talks or activities on frailty will be offered to the participants based on the frailty status.Questionnaire and screening tools will be administered by trained researchers.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A 30-month community survey will be conducted, and the survey will be divided into three phases, namely study preparation and subject recruitment (6 months), data collection (18 months), and data entry and analysis (6 months).
A survey of 15000 people aged 50 years or older identified in community facilities (e.g., neighbourhood elderly centre, social centre for the elderly) will be conducted. The participants will be invited to their affiliated centres for a brief screening using the FRAIL scale and assessment. A series of community health talks or activities on frailty will be offered to the participants based on the frailty status. Questionnaire and screening tools will be administered by trained researchers.
The primary outcome will be the prevalence of frailty and pre-frailty. Secondary outcomes will cover physical performance measures including hand-grip strength and 5-chair stand test. Anthropometric and demographic data will also be collected using standardized methods and questionnaires respectively.
Views of participants taking part in a community health talks or activities on frailty about what the participants felt or had gained from participating, concerns, and suggestions for change or improvement will be explored by client satisfaction questionnaires.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Hong Kong, China
- Chinese University of Hong Kong
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- People aged 50 years or older
- Chinese origin
- Normally reside in Hong Kong
- Could speak and understand Chinese
- Willing to follow the study procedures
Exclusion Criteria:
-Live in a residential aged care facility
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Frailty status
Time Frame: 1 day (Once only at screening)
|
Frailty status (i.e.
robust, prefrail or frail) measured using the frailty scale (FRAIL) in which unabbreviated scale name is unavailable for this scale.
Frailty scores from 0 to 5 (i.e., 1 point for each component; 0 = best to 5 = worst) and represent robust (0), pre-frail (1-2), and frail (3-5) health status.
|
1 day (Once only at screening)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Handgrip strength
Time Frame: 1 day (Once only at screening)
|
Handgrip strength measured using a dynamometer
|
1 day (Once only at screening)
|
|
5 chair stands
Time Frame: 1 day (Once only at screening)
|
Muscle endurance in the lower extremities - Participant will be required to rise from a chair a total of 5 times, as quickly as they could, with arms across their chest.
The amount of time required to complete all 5 repetitions will be recorded.
|
1 day (Once only at screening)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight
Time Frame: 1 day (Once only at screening)
|
Weight in kilogram measured using standardized method
|
1 day (Once only at screening)
|
|
Height
Time Frame: 1 day (Once only at screening)
|
Height in centimeter measured using standardized method
|
1 day (Once only at screening)
|
|
Waist circumference
Time Frame: 1 day (Once only at screening)
|
Waist circumference in centimeter measured using standardized method
|
1 day (Once only at screening)
|
|
Systolic blood pressure
Time Frame: 1 day (Once only at screening)
|
Systolic blood pressure in mmHg measured using standardized method
|
1 day (Once only at screening)
|
|
Diastolic blood pressure
Time Frame: 1 day (Once only at screening)
|
Diastolic blood pressure in mmHg measured using standardized method
|
1 day (Once only at screening)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jean Woo, MD, Chinese University of Hong Kong
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019.475
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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