Actively Recruiting
Reactive Balance Training for Fall Prevention
Led by University of Illinois at Chicago · Updated on 2025-08-24
90
Participants Needed
1
Research Sites
465 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this pilot study is to evaluate and compare the effect of three different perturbation based training devices on the reactive balance control among healthy young adults, healthy older adults, and neurologically impaired stroke individuals. Furthermore, the project aims to determine the feasibility and tolerability of 30-minutes of perturbation training using the SureFooted Trainer. Overall, the project directs to find out the long term effect of training on fall risk reduction and fall prevention. This study investigates the effects of perturbation training (slip and trip) based on the principles of motor learning. Perturbations in the form of slips and trips induced by the three different types of perturbation devices will displace the center of mass outside the base of support and challenge the stability, thereby inducing a fall and demand compensatory strategies in order to prevent it. Such perturbation training would train the motor system to improve stability control and vertical limb support. The project design aims to examine the ability of the central nervous system to mitigate the interference in stability control (if any) that is induced by opposing types of perturbations. The hypothesis of this study if supported by the results, will provide the difference in motor learning with training on three different perturbation devices. Furthermore, it would help to determine which of the three training devices is the most effective in developing defense mechanisms necessary to reduce fall-risk among community-living older adults and the neurological population.
CONDITIONS
Official Title
Reactive Balance Training for Fall Prevention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy young adults aged 18 to 55 years
- Healthy older adults aged 56 to 90 years
- Stroke survivors aged 18 to 90 years with stroke onset over 6 months ago
- No acute or chronic neurological, cardiopulmonary, musculoskeletal, or systemic diagnosis except stroke for stroke survivors
- No recent major surgery within 6 months or hospitalization within 3 months
- Not taking any sedative drugs
- Ability to walk 10 meters with or without an assistive device (for older adults and stroke survivors)
- Ability to understand and communicate in English
- Berg balance scale score less than 45/56 for healthy older adults
You will not qualify if you...
- Heart rate above 85% of age-predicted maximum at baseline
- Resting systolic blood pressure above 165 mmHg or diastolic blood pressure above 110 mmHg at baseline
- Oxygen saturation below 95% at rest
- Body weight over 250 pounds
- Heel bone density with T-score less than -2 (osteoporotic)
- Mild cognitive impairment (Mini-mental State Exam score below 25/30)
- During 6-minute walk test, shortness of breath, uncontrolled pain over 3 on VAS, oxygen saturation below 92%, or inability to achieve age-specified walking distance (for older adults and stroke survivors)
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Illinois at Chicago
Chicago, Illinois, United States, 60612
Actively Recruiting
Research Team
S
Shamali Dusane, MPT
CONTACT
L
Lakshmi Kannan, MS PT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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