Skip to main content
Clinical Trials/NCT05694494
NCT05694494Enrolling By InvitationNot Applicable

Training- and Cost-effectiveness of an Internet-based Lifestyle-integrated Functional Exercise Program (iLiFE) on Reducing Falls, and Promoting Exercise Adherence in Community Older Fallers: a Randomized Controlled Trial

Chinese University of Hong Kong1 site in 1 country322 target enrollmentStarted: May 2, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
322
Locations
1
Primary Endpoint
fall incidence as assessed by monthly telephone or internet follow-up

Study Overview

Brief Summary

Falls are the second leading cause of unintentional injury and death around the globe. About one in every three older adults falls each year worldwide. With the aging population, the cost of treating fall-related injuries is increasing exponentially. There is a pressing need for a cost-effective fall prevention program. Ample evidence has shown the substantial standalone effectiveness of well-designed physical exercises in preventing falls. However, continuous exercise adherence is required for a long-lasting fall prevention effect. Unfortunately, adherence to an exercise program was generally only 21%. Building up the habit of doing regular exercise is thus crucial in preventing falls. Lifestyle integrated Functional Exercise program (LiFE) has been shown to be able to reduce the fall rate by 31% and maintain 64% of the participants exercising at 12 months follow-up. This proposed randomized controlled trial aims at comparing the effectiveness of an internet-based LiFE in reducing subsequent falls and promoting exercise adherence in community-dwelling older adults.

Detailed Description

All subjects will then be randomly assigned to receive either an internet-based therapist-led LiFE program with a home environment safety assessment (iLiFE) or attention control intervention. Randomization into block groups of four in a 1:1 ratio (the iLiFE group or the attention control group) will be generated in a password-protected excel file by independent research personnel not involved in data collection or intervention after the baseline assessment. The randomization will be concealed by the independent personnel. Research assistants who are blinded to the group allocation will conduct all the subsequent monthly surveillance and assessments at baseline and follow-up sessions. All data will also be entered and checked by the blinded research assistants. All procedures concur with the Declaration of Helsinki (2013).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •aged ≥ 65 years,
  • •community-dwelling,
  • •have a fall history in the previous 12 months,
  • •have a moderate or above risk of falls as assessed by the Physiological Profile Assessment (total z-score ≥ 1)
  • •can ambulate on level surfaces without physical contact of another person as assessed by Functional Ambulation Category (score ≥ 3)
  • •cognitively intact as assessed by the Hong Kong version of the Montreal Cognitive Assessment-5-minute protocol (score ≥ 16th percentile of the age and education-adjusted cut-off score)
  • •able to communicate effectively.

Exclusion Criteria

  • •uncorrected vision or hearing impairment,
  • •unstable medical condition that may preclude the planned exercises, and
  • •have been receiving or planning to receive any fall prevention program within the study period.

Arms & Interventions

iLiFE

Experimental

receiving Lifestyle-integrated Functional Exercise training and home safety assessment

Intervention: internet-based Lifestyle-integrated Functional Exercise (iLiFE) (Behavioral)

attention control

Placebo Comparator

upper limb exercise training

Intervention: upper limb exercise training (Behavioral)

Outcomes

Primary Outcomes

fall incidence as assessed by monthly telephone or internet follow-up

Time Frame: 12 months

Secondary Outcomes

  • health-related quality of life as assessed by EQ-5D-5L(12 months)
  • mobility as assessed by the Ten Metre Walk Test(4 months)
  • muscle mass as assessed by the Bioimpedance Analysis (BIA)(4 months)
  • postural hypotension as assessed by the blood pressure in sitting and standing(4 months)
  • physiological fall risk as assessed by the Physiological Profile Assessment (PPA)(4 months)
  • Cognitive flexibility as assessed by Trail Making Test(4 months)
  • balance confidence as assessed by the Short version of the Chinese version of the Activities-specific Balance Confidence Scale(12 months)
  • balance as assessed by the 4-stage stance(4 months)
  • physical activity level as assessed by thigh-worn accelerometer (ActivPAL4 physical activity monitor, PAL Technologies Ltd., Glasgow, UK)(4 months)
  • exercise adherence as assessed by Section B of the Exercise Adherence Rating Scale(12 months)
  • balance as assessed by functional reach tests(4 months)
  • mobility as assessed by the Short Physical Performance Battery Test(4 months)
  • mobility as assessed by the Timed Up and Go Test(4 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Timothy Kwok

Professor

Chinese University of Hong Kong

Study Sites (1)

Loading locations...

Similar Trials