Postural Control in Adults
Part of paid clinical trials in Oklahoma City, Oklahoma.
- Sponsor
- University of Oklahoma
- Study ID
- NCT07554118
- Status
- Recruiting
Conditions
- Adults
- Older
- Older Adults, Balance
Eligibility Criteria
- Sex
- ALL
- Age
- 65 Years - 80 Years
- Healthy Volunteers
- Accepted
Interventions
- restricted vision (no-V) — BEHAVIORALno-V group will perform the dynamic balance task with blind-fold. The 2 weeks dynamic balance training involves standing and maintaining balance on a stabilometer, which consists of a platform (1.3m long by 1.4m wide) connected to a single axis that allows bidirectional sway (Lafayette Instrument Co.; Fig. 2). The maximum angular deviation of the platform is 18°. A safety harness may be provided to prevent falls but does not provide support during the performance of the task. Participants are required to maintain balance with feet in a medio-lateral orientation while standing on the balance board. A potentiometer monitors the sway angle of the platform. An integrated timer measures time in balance, which is defined as when the platform angle is within ± 5° of horizontal. The participants will be encouraged to maintain the platform in horizontal for as long as possible within a 30 s trial. Participants assigned to no-V group will perform the task with blind-fold.
- full vision (full-V) — BEHAVIORALThe participants will be performing the dynamic balance training with their full vision.
Study Details
The investigators propose a 2-week intervention involving adults over 65 years old. Participants will undergo dynamic balance training on an movable platform (stabilometer) with either restricted or full vision. The primary objective is to facilitate sensory re-weighting, hypothesizing that restricted vision training will increase somatosensory input utilization for postural control. Pre- and post-training assessments will measure postural control during gait initiation under a dual-task condition. The investigators hypothesize that the restricted vision group will demonstrate: 1. Improved postural control, indicated by increased center of pressure displacement during gait initiation. 2. Improved ability to utilize somatosensory input during a balance task.
Key Dates
- Start date
- Jan 30, 2026
- Status verified
- Apr 2026
- Primary completion
- Oct 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: restricted vision (no-V)The participant will be blind-folded in the following dynamic balance training. The 2 weeks dynamic balance training involves standing and maintaining balance on a stabilometer, which consists of a platform (1.3m long by 1.4m wide) connected to a single axis that allows bidirectional sway (Lafayette Instrument Co.; Fig. 2). The maximum angular deviation of the platform is 18°. A safety harness may be provided to prevent falls but does not provide support during the performance of the task. Participants are required to maintain balance with feet in a medio-lateral orientation while standing on the balance board. A potentiometer monitors the sway angle of the platform. An integrated timer measures time in balance, which is defined as when the platform angle is within ± 5° of horizontal. The participants will be encouraged to maintain the platform in horizontal for as long as possible within a 30 s trial. Participants assigned to no-V group will perform the task with blind-fold.
- Active Comparator: full vision (full-V)The participants in this arm will be doing the dynamic balance training with eyes open. The 2 weeks dynamic balance training involves standing and maintaining balance on a stabilometer, which consists of a platform (1.3m long by 1.4m wide) connected to a single axis that allows bidirectional sway (Lafayette Instrument Co.; Fig. 2). The maximum angular deviation of the platform is 18°. A safety harness may be provided to prevent falls but does not provide support during the performance of the task. Participants are required to maintain balance with feet in a medio-lateral orientation while standing on the balance board. A potentiometer monitors the sway angle of the platform. An integrated timer measures time in balance, which is defined as when the platform angle is within ± 5° of horizontal. The participants will be encouraged to maintain the platform in horizontal for as long as possible within a 30 s trial. Participants assigned to no-V group will perform the task with blind-fold
Primary Outcome Measure
Dynamic postural control [ Time Frame: From enrollement to one week within the last training days (within 3 weeks from enrollment) ]
Central Contacts
- Yo Shih, PhD405-271-2131
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Oklahoma Health Sciences Center | Oklahoma City | Oklahoma | 73117 |
Find similar trials in Oklahoma City, OK
Related Studies
- PhoRTE® Therapy Efficacy: In-Person Versus TelehealthNot Yet Recruiting · University of Southern California · Arcadia, California
- Adapting, Implementing and Evaluating the Effectiveness of HARP for People With DisabilitiesRecruiting · Washington University School of Medicine · St Louis, Missouri
- Mindfulness Walking Intervention to Enhance Resilience (iWalk)Recruiting · University of Illinois at Urbana-Champaign · Urbana, Illinois
- Study of LGW16-03 To Identify NervesPHASE1 · Recruiting · Eric R. Henderson · Lebanon, New Hampshire