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Motion tracking virtual reality technology in improving gait in the elderly: A randomized controlled trial
Objective This study aimed to assess the effectiveness of virtual reality-based treadmill training on gait performance and tolerance in the elderly. Design Two-armed randomized controlled trial. Setting The Medical Rehabilitation Sciences Department, Umm Al Qura University, Saudi Arabia. Participant...
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Published in: | Clinical rehabilitation 2024-04, Vol.38 (4), p.520-529 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Objective
This study aimed to assess the effectiveness of virtual reality-based treadmill training on gait performance and tolerance in the elderly.
Design
Two-armed randomized controlled trial.
Setting
The Medical Rehabilitation Sciences Department, Umm Al Qura University, Saudi Arabia.
Participants
Sixty Saudi elderly of both sexes, aged 65–75 years, were included.
Interventions
Participants were divided into two groups. The control group received treadmill training without virtual reality, alongside a conventional exercise program. The experimental group received a training program that was similar to the control group's exercises but with C-Mill virtual reality treadmill training. The program lasted one hour, three times per week, over four consecutive weeks.
Main Measures
The study assessed changes in outcome measures at baseline, Post-1 (after four weeks of training), and Post-2 (four weeks post-training). These measures encompassed the primary outcome, the 6-minute walk test (meter), as well as secondary outcomes such as stride length (meter), stride time (second), cadence (steps/minute), and velocity (meter/second). These parameters were evaluated using the GaitRite electronic gait analysis walkway.
Results
The experimental group showed better improvement in the mean values of the 6-minute walk test, stride length, stride time, cadence, and velocity compared to the control group at post-1 and post-2. The P-values were respectively at post-1 (0.019, 0.015, 0.041, 0.013, and 0.021) and (0.011, 0.025, 0.073, 0.061, and 0.017) at post-2 (all, P |
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ISSN: | 0269-2155 1477-0873 |
DOI: | 10.1177/02692155231217468 |