Reactive Balance Training for Fall Prevention
Launched by UNIVERSITY OF ILLINOIS AT CHICAGO · Dec 18, 2019
Trial Information
Current as of August 20, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a type of training designed to help people improve their balance and reduce the risk of falls. Researchers will compare three different devices that create slips and trips to see which one works best in helping healthy young adults, older adults, and individuals who have had a stroke. The hope is that by practicing with these devices, participants can learn to control their balance better and feel more secure while moving around.
To be eligible for the trial, participants should be aged 18-90 years and generally healthy, without serious medical conditions or recent surgeries. For older adults, they need to be able to walk at least 10 meters, while stroke survivors must have had their stroke more than six months ago. Participants can expect to take part in 30-minute sessions of balance training and will be closely monitored throughout the study. This research aims to find effective ways to keep people safe from falls, which is especially important for maintaining independence as we age.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Healthy Young participants
- • Age group: 18-55 years.
- • Absence of any acute or chronic neurological, cardiopulmonary, musculoskeletal or systemic diagnosis.
- • No recent major surgery (\< 6 months) or hospitalization (\< 3 months)
- • Not on any sedative drugs.
- • Can understand and communicate in English
- • Healthy older adults
- • Age group: 56-90 years.
- • Absence of any acute or chronic neurological, cardiopulmonary, musculoskeletal or systemic diagnosis.
- • No recent major surgery (\< 6 months) or hospitalization (\< 3 months)
- • Not on any sedative drugs.
- • Ability to walk with or without an assistive device for 10 meters
- • Can understand and communicate in English
- • Berg balance scale score \<45/56.
- • Persons with stroke
- • Age group: 18-90 years.
- • Absence of any acute or chronic neurological diagnosis except stroke (self reported)
- • Onset of stroke (\> 6 months)
- • Absence of any cardiopulmonary, musculoskeletal or systemic diagnosis.
- • No recent major surgery (\< 6 months) or hospitalization (\< 3 months)
- • Not on any sedative drugs.
- • Ability to walk with or without an assistive device for 10 meters
- • Can understand and communicate in English
- Exclusion Criteria:
- Healthy subject:
- • Subjects will not proceed with the test if any of the following occurs at baseline measurement: 1) HR \> 85% of age-predicted maximal heart rate (HRmax) (HRmax = 220 - age), 2) systolic blood pressure (SBP) \> 165 mmHg and/or diastolic blood pressure (DBP) \> 110 mmHg during resting), and 3) oxygen saturation (measured by pulse oximeter) during resting \< 95%.
- • Body weight more than 250 lbs.
- Healthy Older adults:
- • Individuals with heel bone density with a T-score \< -2, is classified as osteoporotic and will be excluded.
- • Individuals with mild cognitive impairment (Mini-mental State Exam score \< 25/30) will be excluded.
- • Subjects will not proceed with the test if any of the following occurs at baseline measurement: 1) HR \> 85% of age-predicted maximal heart rate (HRmax) (HRmax = 220 - age), 2) systolic blood pressure (SBP) \> 165 mmHg and/or diastolic blood pressure (DBP) \> 110 mmHg during resting), and 3) oxygen saturation (measured by pulse oximeter) during resting \< 95%.
- • 6 minute walk test. Subjects will also be screened out if on the 6 minute walk test they complain of shortness of breath or uncontrolled pain (\> 3/10 on VAS) or pulse oxygen drops \< 92% or are unable to achieve the age-specified minimal ambulation distance.
- • Body weight more than 250 lbs.
- Persons with stroke:
- • Individuals with heel bone density with a T-score \< -2, is classified as osteoporotic and will be excluded.
- • Individuals with mild cognitive impairment (Mini-mental State Exam score \< 25/30) will be excluded.
- • Subjects will not proceed with the test if any of the following occurs at baseline measurement: 1) HR \> 85% of age-predicted maximal heart rate (HRmax) (HRmax = 220 - age), 2) systolic blood pressure (SBP) \> 165 mmHg and/or diastolic blood pressure (DBP) \> 110 mmHg during resting), and 3) oxygen saturation (measured by pulse oximeter) during resting \< 95%.
- • 6 minute walk test. Subjects will also be screened out if on the 6 minute walk test they complain of shortness of breath or uncontrolled pain (\> 3/10 on VAS) or pulse oxygen drops \< 92% or are unable to achieve the age-specified minimal ambulation distance.
- • Body weight more than 250 lbs.
About University Of Illinois At Chicago
The University of Illinois at Chicago (UIC) is a leading academic institution renowned for its commitment to advancing health sciences through innovative research and clinical trials. With a strong emphasis on interdisciplinary collaboration, UIC harnesses the expertise of its diverse faculty and state-of-the-art facilities to conduct cutting-edge clinical studies aimed at improving patient outcomes. The university's robust infrastructure for clinical research, combined with its dedication to ethical standards and regulatory compliance, positions UIC as a pivotal contributor to the development of new treatments and therapies in various medical fields. Through strategic partnerships and community engagement, UIC strives to translate research findings into real-world applications, enhancing the health and well-being of populations locally and globally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chicago, Illinois, United States
Patients applied
Trial Officials
Tanvi Bhatt, PhD
Principal Investigator
University of Illinois at Chicago
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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