- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06672640
Effects of Remote Exercise on Physical Function in Pre-Frail Older Adults
November 1, 2024 updated by: Kyeongjin Lee, Kyungdong University
Effects of Remote Exercise on Physical Function in Pre-Frail Older Adults: A Randomized Controlled Trial
This study aims to compare the effects of remote versus in-person exercise interventions on physical function, balance, gait stability, and fall efficacy in pre-frail older adults aged 65 years and above.
Participants are randomly assigned to either a remote exercise group, an in-person exercise group, or a control group.
The exercise intervention includes balance, strength, and gait training conducted twice weekly for eight weeks.
The control group receives educational materials on physical activity.
The primary outcome measures include assessments of balance, lower limb strength, gait ability, and fall efficacy.
This study seeks to determine if remote exercise is as effective as in-person exercise in enhancing physical function in pre-frail older adults, potentially providing a feasible alternative to traditional in-person programs and addressing barriers such as limited mobility and access to exercise facilities.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
90
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Gangwon-do
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Wonju, Gangwon-do, Korea, Republic of, 26495
- Department of Physical Therapy, Kyungdong University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Aged 65 years or older
- Classified as pre-frail based on Fried's frailty criteria (meeting at least two out of five specified indicators)
- Experienced a fall in the preceding six months or have impaired gait and balance (TUG ≥ 13.5 seconds, BBS ≤ 45)
- Mini-Mental State Examination (MMSE) score of 24 or higher
- Demonstrate the physical capacity to engage in the remote exercise (e.g., ability to stand from a seated position and walk short distances)
Exclusion Criteria:
- Neurological or musculoskeletal conditions that impede physical activity
- Recent history of severe cardiovascular disease (within the past three months)
- Inability to commit to continuous participation throughout the study period
- Any other medical condition that might interfere with the intervention or pose a risk to the participant
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: remote exercise group
Participants in the remote exercise group will engage in exercise sessions conducted twice weekly for eight weeks using video conferencing software.
The intervention includes balance, strength, and gait training, supervised by a licensed physical therapist.
Sessions are performed at participants' homes with assistance from caregivers to ensure safety and compliance.
|
Participants in this group will engage in an eight-week exercise program conducted via video conferencing software.
The sessions, which focus on balance, lower limb strength, and gait function, will be held twice weekly for 50 minutes each.
Licensed physical therapists will supervise the sessions, and participants will exercise at home, with assistance from caregivers if necessary.
The program aims to evaluate the effectiveness of remote exercise interventions in improving physical function and reducing the risk of falls in pre-frail older adults.
|
|
Experimental: in-person exercise group
Participants in the in-person exercise group will attend supervised exercise sessions at a senior welfare center twice weekly for eight weeks.
The sessions, conducted by a licensed physical therapist, focus on improving balance, lower limb strength, and gait stability.
The intervention is identical to the remote exercise group, except the mode of delivery is in person at the welfare center.
|
Participants in this group will take part in an eight-week in-person exercise program at a senior welfare center.
The sessions will be held twice weekly for 50 minutes and will be led by a licensed physical therapist.
The exercise program, which includes balance, lower limb strength, and gait training, is identical to that of the remote exercise group, with the primary difference being the mode of delivery (in-person at the welfare center).
This group aims to assess the effectiveness of direct supervision in a controlled environment.
|
|
Other: control group
Participants in the control group will receive an informational booklet on exercise and attend a single educational session about physical activity.
They will be encouraged to maintain their usual activities, and their physical activity levels will be self-reported and periodically monitored by the research team.
|
Participants in this group will receive educational materials about physical activity, including a booklet and one educational session.
They will not participate in any structured exercise program but will be encouraged to maintain their usual activities.
The control group serves as a baseline to compare the outcomes of exercise interventions against no structured exercise, focusing on evaluating usual care versus targeted exercise programs.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance ability
Time Frame: Baseline and post-intervention at 8 weeks
|
Balance performance will be assessed using the Timed Up and Go (TUG) test and Berg Balance Scale (BBS).
The TUG measures the time taken for a participant to stand up from a chair, walk three meters, turn around, walk back, and sit down.
The BBS is a comprehensive assessment of balance ability during various tasks.
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Baseline and post-intervention at 8 weeks
|
|
Lower Limb Strength
Time Frame: Baseline and post-intervention at 8 weeks
|
Lower limb strength will be evaluated using the Five Times Sit-to-Stand Test (FTSTS) and the 30-Second Chair Stand Test (30SCS).
The FTSTS measures the time it takes for participants to rise from a chair five times, and the 30SCS measures the number of times participants can rise from a chair in 30 seconds.
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Baseline and post-intervention at 8 weeks
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Gait Ability
Time Frame: Baseline and post-intervention at 8 weeks
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Gait ability will be assessed using the Dynamic Gait Index (DGI) and the 10-Meter Walk Test (10MWT).
The DGI assesses participants' ability to modify balance while walking in response to external demands, and the 10MWT measures the time taken to walk 10 meters at a comfortable speed.
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Baseline and post-intervention at 8 weeks
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Fall Efficacy
Time Frame: Baseline and post-intervention at 8 weeks
|
Fall efficacy will be measured using the Modified Falls Efficacy Scale (MFES).
This scale evaluates participants' confidence in performing daily activities without falling, providing an indication of fall-related self-efficacy.
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Baseline and post-intervention at 8 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2023
Primary Completion (Actual)
December 31, 2023
Study Completion (Actual)
December 31, 2023
Study Registration Dates
First Submitted
November 1, 2024
First Submitted That Met QC Criteria
November 1, 2024
First Posted (Estimated)
November 4, 2024
Study Record Updates
Last Update Posted (Estimated)
November 4, 2024
Last Update Submitted That Met QC Criteria
November 1, 2024
Last Verified
November 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2024-05-014
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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