- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05993013
Improving Strength and Balance Through Exercise With LudoFit
Improving Strength and Balance in Older Adults at Risk of Falls With the LudoFit Exercise Program
The goal of this mixed methods cohort study is to explore how an innovative game-based, technology-enabled home exercise software compares to a conventional home-based exercise program in older adults at risk for falls. The main question[s] it aims to answer are:
- Does the exercise software lead to better or similar adherence to exercise recommendations compared to the conventional exercise program?
- Does the exercise software improve user strength and balance, as measured by relevant physical function scores?
- Do participants find the exercise software enjoyable and acceptable?
Participants will be approached during their initial fall risk assessment to see if they are interested in taking part. Those who agree to participate will choose either the exercise software or the conventional exercise program and will be instructed to:
- Perform their respective exercise program for a minimum of 3 times a week for 3 months.
- Return to clinic in 3 months to see our C-FAST physiotherapist for reassessment of their relevant physical functional tests.
- For conventional exercise program only - Document exercise compliance in an exercise log.
- For software program only - Complete a survey regarding the use of the technology.
Researchers will compare software-use cohort versus conventional exercise program cohort to see if adherence and physical function scores are comparable.
Study Overview
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Shirley Huang, MD, FRCPC, MSc, MSc (HQ)
- Phone Number: 14195 613-798-5555
- Email: shhuang@toh.ca
Study Locations
-
-
Ontario
-
Ottawa, Ontario, Canada, K1Y4E9
- Recruiting
- The Ottawa Hospital
-
Contact:
- Shirley CC Huang
- Phone Number: 613-761-4645
- Email: shhuang@toh.ca
-
Contact:
- Taryn Mackenzie
- Phone Number: 10225 613-798-5555
- Email: tmackenzie@toh.ca
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patient is interested in a home-based exercise program.
- The patient is independent with activities of daily living and instrumental activities of daily living.
- Patient agrees to return for 3-month follow-up.
- Patient must speak English or French.
Exclusion Criteria:
Patient has the following physical functional performance:
- Berg Balance Scale score of 45 or less
- Unable to safely and independently reach at least 5 inches to the side and forward
- Unable to safely and independently reach down, touch floor and then return to start position
- Patient has diagnosed or suspected cognitive impairment.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Conventional exercise
Normally physiotherapist-recommended, tailored strength and balance exercises.
These exercises are given in printed handouts and demonstrated by our physiotherapist with the patients during their initial clinic visit.
Exercise is recommended to be done at least 3 times per week.
|
|
|
Experimental: Game-based exercise
Strength and balance exercises using the LudoFit game-based exercise software.
Participants will be registered on the platform.
Exercise is recommended to be done at least 3 times per week.
|
Game-based, technology-enabled home exercise software, done at least 3 times per week.
Video games for a variety of exercises that promote balance, strength, endurance, and coordination.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical function test 1-Berg Balance Scale
Time Frame: 3 months
|
Berg Balance Scale is a series of balance maneuvers administered by a physiotherapist to assess the balance of a subject.
It is scored from 0 to 56.
The higher the score the better the balance.
Subject scores are also compared to age-matched normative values.
This measure will be collected at initial clinic visit and then again at 3-month follow-up visit and the values compared for any improvement.
|
3 months
|
|
Physical function test 2-Timed Up and Go Test
Time Frame: 3 months
|
Timed Up and Go Test documents time taken in seconds for a subject stand up from a chair, walk 3 meters forward and then return to the chair and sit down.
The longer the time taken, the worse the outcome.
Taking over 14 seconds in Timed Up and Go Test correlates with increased risk of falls.
This measure will be collected at initial clinic visit and then again at 3-month follow-up visit and the values compared for any improvement.
|
3 months
|
|
Physical function test 3-Five Time Sit to Stand Test
Time Frame: 3 months
|
Five Times Sit to Stand test scoring is based on the amount of time (to the nearest decimal in seconds) a subject is able to transfer from a seated to a standing position and back to sitting five times.
The lower the time to complete the test the better the outcome of the test.
Subject scores are also compared to age-matched normative values.
This measure will be collected at initial clinic visit and then again at 3-month follow-up visit and the values compared for any improvement.
|
3 months
|
|
Conventional exercise cohort - Exercise adherence
Time Frame: 3 months
|
Participants will be given an exercise log at the beginning of the study and asked to use this log to document frequency of exercise each week, minutes spent during each exercise session and any additional comments/feedback about each exercise session (e.g.
any discomfort or difficulty performing the exercise).
The researchers will collect the exercise log at the 3-month follow-up visit and the entries analyzed.
The more frequently the exercises were performed measured in total number of days per week and total minutes spent exercising, the better.
Any qualitative comments provide by subjects in the log will be collected and analyzed for any themes.
|
3 months
|
|
LudoFit exercise cohort - Exercise adherence
Time Frame: 3 months
|
LudoFit software automatically tracks user exercise adherence data, including minutes of use per day, as well as performance in each activity and rate of perceived exertion.
This data will be downloaded by researchers and analyzed.
The more frequently the exercises were performed measured in total number of days per week and total minutes spent exercising, the better.
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Satisfaction with LudoFit exercise software
Time Frame: 3 months
|
Participants will be given a standardized paper survey to complete at the 3-month follow-up visit where they will answer questions pertaining to their user experience with the software, such as acceptability and usability.
The survey includes both quantitative (13 statements where subjects rate their agreement with the statements on a 5-point Likert scale; the higher the score, the higher the agreement with the statement) and qualitative components (subjects can provide additional comments to express what they find most beneficial with using LudoFit software and what could have made their experience with LudoFit better).
|
3 months
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Other Study ID Numbers
- 4829
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.
Clinical Trials on Accidental Falls
-
The Hospital District of SatakuntaCompleted
-
University Hospital, Strasbourg, FranceRecruitingAccidental FallsFrance
-
Sigma Theta Tau InternationalRecruiting
-
University of Maryland, BaltimoreVA Maryland Health Care SystemCompletedAccidental FallsUnited States
-
Washington University School of MedicineUS Department of Housing and Urban DevelopmentCompleted
-
Universidad Miguel Hernandez de ElcheSocio- Health Center Puente Real ( Health Care for Older © ) of BadajozCompleted
-
The Hong Kong Polytechnic UniversityCompletedAccidental FallsHong Kong
-
Montana State UniversityCompletedAccidental FallsUnited States
-
University of PittsburghBoston University; Foundation for Physical Therapy, Inc.; Mt. Ascutney Hospital...CompletedAccidental FallsUnited States
-
Duke UniversityNational Institute of Nursing Research (NINR); The Carolinas Center for Medical...CompletedAccidental FallsUnited States