Obstacle Negotiation in Older People With and Without Vision Impairment
Part of paid clinical trials in Bloomington, Indiana.
- Sponsor
- Indiana University
- Study ID
- NCT05888441
- Status
- Recruiting
Conditions
- Low Vision
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Obstacle characteristics — OTHERIn the walking trials, when an obstacle is present, the obstacle height and obstacle contrast level will be varied across the trial repetitions. Each participant will be exposed to obstacles of two heights: the first will be 1 centimeter in height, and the second will be approximately 20% of the subject's leg length (ranging in physical height between 15 - 22 centimeters to cover a range of leg lengths in the population). Obstacles (of both heights) will also be painted such that their measured luminance (or contrast) level against the floor luminance is varied. High contrast obstacles will have ≥80% Michelson contrast and low contrast obstacles will have ≤30% Michelson contrast.
Study Details
Falls are common among people with vision impairment and can lead to devastating health consequences. Understanding the functions of vision and how the visual characteristics of obstacles in the walking path impact the gait of people with vision impairment is necessary to create strategies to prevent falls in this population. The purpose of this study is to determine how adults with vision impairment change their gait behavior when stepping over obstacles that vary in height and contrast to the ground. We will then determine the mechanisms of gaze behavior that correlate to the gait behavior.
Key Dates
- Start date
- Apr 14, 2023
- Status verified
- Nov 2025
- Primary completion
- Dec 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 200 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: Low Vision GroupAt a single study visit, the group of low vision participants will be asked to perform a series of short walking trials. During each trial they will walk at a self-selected speed along a walkway (6 meters in length) that may or may not contain an obstacle to step over. The trials will be randomly varied with regard to an obstacle's presence, height, and contrast from the walkway surface. Repeated trials of each condition variation will be performed during the visit.
- Active Comparator: Control GroupAt a single study visit, the group of age-matched participants without low vision will be asked to perform a series of short walking trials. During each trial they will walk at a self-selected speed along a walkway (6 meters in length) that may or may not contain an obstacle to step over. The trials will be randomly varied with regard to an obstacle's presence, height, and contrast from the walkway surface. Repeated trials of each condition variation will be performed during the visit.
Primary Outcome Measure
Vertical foot clearance, lead limb [ Time Frame: During a single intervention visit (Study Visit 2), up to 2-3 hours in duration. ]
Central Contacts
- Kierstyn A Napier-Dovorany, OD8128554426
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Indiana University | Bloomington | Indiana | 47405 |
Find similar trials in Bloomington, IN
Related Studies
- Socially Assistive Robots to Enhance Magnification Device Use for ReadingPHASE1 · Recruiting · University of California, Los Angeles · Los Angeles, California
- Beacon Sensors and Telerehabilitation to Assess and Improve Use of Devices (BeST-AID) for Low VisionRecruiting · University of California, Los Angeles · Fullerton, California
- Wearable Echolocation Aids Using Parametric SoundRecruiting · The University of Texas Medical Branch, Galveston · Galveston, Texas
- Vision Rehabilitation Training With Multimodal Feedback in Central Vision LossRecruiting · New England College of Optometry · Boston, Massachusetts