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Clinical Trials/NCT04139837
NCT04139837
Completed
N/A

Frailty in Daily Practice: Screening, Consultation and Education Activities

Chinese University of Hong Kong1 site in 1 country5,951 target enrollmentJanuary 3, 2020
ConditionsFrailty

Overview

Phase
N/A
Intervention
Not specified
Conditions
Frailty
Sponsor
Chinese University of Hong Kong
Enrollment
5951
Locations
1
Primary Endpoint
Frailty status
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

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.

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.

Registry
clinicaltrials.gov
Start Date
January 3, 2020
End Date
May 25, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jean Woo

Professor

Chinese University of Hong Kong

Eligibility Criteria

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

Outcomes

Primary Outcomes

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.

Secondary Outcomes

  • Handgrip strength(1 day (Once only at screening))
  • 5 chair stands(1 day (Once only at screening))

Study Sites (1)

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