Impact of a new sock design on ankle and balance stability
Effectiveness of a Novel Sock Design on Ankle and Postural Stability
This study tests if a new sock design can help adults improve their ankle stability and balance while also seeing if it makes them feel more confident during balance exercises.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Central Florida Academic / other |
| Locations | 1 site (Orlando, Florida) |
| Trial ID | NCT06871085 on ClinicalTrials.gov |
What this trial studies
This study investigates how a novel sock design affects ankle stability and overall postural stability in adults. Using a prospective cohort design, participants will be assessed on their functional performance and muscle activation while wearing the sock compared to not wearing it. The study also aims to measure subjective changes in participants' confidence levels when performing balance exercises. Participants will undergo screening to ensure eligibility and will provide informed consent before participating.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who can perform specific physical activities without pain or discomfort.
Not a fit: Patients with recent ankle injuries, surgeries, or existing foot conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance ankle stability and improve balance in individuals, potentially reducing the risk of falls.
How similar studies have performed: While similar studies on stability interventions exist, the specific approach of using a novel sock design is relatively novel and untested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Minimum of 18 years old or older * Able to perform the following actions with no pain or discomfort: sit-to-stand, jump, one leg stand * Must read, write, and speak sufficient English in order to complete subjective questionnaire Exclusion Criteria: * Had a previous foot or leg injury * Had a foot condition at the time of their participation in the study * Had feelings of instability at the ankle * Had an ankle injury within the past 12 months * Had surgery on either lower extremity in the past * Had any torn ligaments or cartilage at the hip, knee, or ankle * Experienced radicular symptoms down either lower extremity * Had any allergies to the sock material used in the study 1. 80% nylon 2. 14% polyester 3. 6% elastane * Is currently pregnant
Where this trial is running
Orlando, Florida
- University of Central Florida — Orlando, Florida, United States (Recruiting)
Study contacts
- Study coordinator: William J Hanney, PhD
- Email: william.j.hanney@ucf.edu
- Phone: 407-823-0217
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.