Actively Recruiting
Neuromechanisms of Falls in Older Adults With Mild Cognitive Impairment: Assessment and Training of Reactive Balance Control
Led by University of Illinois at Chicago · Updated on 2024-11-26
142
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
Sponsors
U
University of Illinois at Chicago
Lead Sponsor
N
National Institute on Aging (NIA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to study older adults with mild cognitive impairment (OAwMCI) who often have more balance and walking problems than cognitively intact older adults (CIOA), leading to a higher risk of falls and reduced mobility. The study focuses on understanding how combined cognitive and physical challenges affect balance and brain function, aiming to improve fall prevention strategies using new training methods. The study is a stage 1 pilot designed to test the feasibility and effects of a novel training approach. Participants will engage in a dual-task perturbation training using a motorized treadmill that delivers controlled balance disturbances while they perform cognitive tasks. The training includes playing cognitive games targeting memory, executive function, visuomotor skills, and language while standing and walking. Participants will experience slips on the treadmill both with and without cognitive tasks to train reactive stepping and balance control. The study includes single and multiple session groups over four weeks. During the study, participants will be assessed on their balance, muscle responses, walking patterns, and cognitive function before, immediately after, and four weeks following training. Measurements include stability during slips, walking step length and cadence, accuracy on cognitive tests, brain imaging, and questionnaires on physical activity and perceived task load. The study also monitors safety through heart rate, blood pressure, and oxygen levels. The total involvement lasts at least four weeks with follow-up assessments to evaluate lasting effects on fall risk and mobility.
CONDITIONS
Brief Title
Dual Task Perturbation Training for OAwMCI
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Older adults aged 55 years or older
- Mild cognitive impairment defined by MOCA score less than 26 out of 30 or cognitively intact with MOCA above 26
- No acute or chronic neurological (e.g., stroke, Parkinson's, Alzheimer's), cardiopulmonary, musculoskeletal, or systemic diagnoses
- No recent major surgery within 6 months or hospitalization within 3 months
- Not currently taking sedative medications
- Ability to understand and communicate in English
- Ability to walk more than 10 meters without an assistive device
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
- Resting oxygen saturation below 90%
- History of bone fracture or significant systemic disease or surgery in the last six months
- For MRI participants: presence of pacemaker, metal implants except orthopedic, claustrophobia, or incompatible cataract surgery
- Weight over 220 lbs (harness weight limit)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 4 weeks
Participants undergo dual task perturbation training involving cognitive games and treadmill-induced slips to improve reactive balance and fall-resisting skills.
Weekly visits for up to 4 weeks
Duration - At least 3 months post-treatment
Participants are monitored for sustained improvements in stability control, cognition, and fall reduction after completing the training.
Approximately 1 to 2 visits during follow-up period
Trial Site Locations
Total: 1 location
1
University of Illinois at Chicago
Chicago, Illinois, United States, 60612
Actively Recruiting
Research Team
T
Tanvi S Bhatt
L
Lakshmi Kannan
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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