Actively Recruiting
Sensor Ankle Brace for Special Operations Rehabilitation
Led by Indiana University · Updated on 2025-10-23
60
Participants Needed
1
Research Sites
35 weeks
Total Duration
On this page
Sponsors
I
Indiana University
Lead Sponsor
T
TAYCO BRACE, INC
Collaborating Sponsor
AI-Summary
What this Trial Is About
The primary purpose of this study is to conduct a clinical trial to test a prototype device for feasibility and not health outcomes. To do this, the investigators will evaluate the performance of commercially available inertial measurement unit sensors incorporated into an existing ankle brace ("sXAB") by TayCo Brace, Inc. We will compare the gait metrics calculated from the sensors incorporated into the brace with gold-standard equipment that is used in research and clinical settings to determine whether the sXAB performs adequately in terms of measurement or technical feasibility prior to further clinical evaluation. The sensors in the ankle brace will be validated in the lab, first on healthy subjects walking in standard tennis shoes/sneakers (protocol 1), and secondarily in the lab on healthy subjects wearing combat boots performing walking, running, jumping, and stair climbing (protocol 2). These movements were selected because they simulate key movements performed during operational activities. Protocol 1 will take place first, then aspects of the sXAB will be evaluated and implemented, then protocol 2 will take place. Participants completing protocol 1 are eligible to complete protocol 2. The study includes two cohorts of participants completing different functional tasks. All participants experience both conditions: with an ankle brace and without an ankle brace. Comparisons are made within-subject between brace and no-brace conditions. It is hypothesized that the sensor-enabled ankle brace will measure gait metrics with a high degree of accuracy (within 5%) when compared against the gold-standard lab equipment (i.e., motion capture and research-grade inertial measurement units).
CONDITIONS
Official Title
Sensor Ankle Brace for Special Operations Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy adults aged 18 to 40 years
- Considered healthy to exercise as determined by the physical activity readiness questionnaire (PAR-Q)
- For cohort 2 only: Moderate or high activity level based on the International Physical Activity Questionnaire - Short Form (IPAQ)
- For cohort 2 only: Ability to comfortably fit into combat boots provided by the laboratory (Men's sizes 8-12, Women's sizes 6-10, foot length 22.54-29.27 cm)
You will not qualify if you...
- Regular tobacco smoking
- Previous lower back or lower limb surgery including joints of pelvis and lower limbs
- Musculoskeletal injury within 12 weeks prior to enrollment causing physical activity reduction for at least 3 days and no pain-free return for 6 weeks
- Pregnant women
- Current or history of unresolved musculoskeletal, neurological, cardiovascular, pulmonary/respiratory, metabolic, or renal conditions
- Torn anterior or posterior cruciate ligament (ACL or PCL)
- Any other disease or problem affecting movement or ability to exercise even at low intensity
- For cohort 2 only: Identification of Functional Ankle Instability (IDFAI) score less than 11
- For cohort 2 only: Unable to comfortably perform drop landing condition
- For cohort 2 only: Feet too large or small to fit combat boots provided
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Indiana University, School of Public Health - Bloomington
Bloomington, Indiana, United States, 47405
Actively Recruiting
Research Team
A
Allison H Gruber, PhD
CONTACT
A
Adriana M Alamilla, MS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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