Skip to content

Effects of Two Compression Socks on Balance and Ankle Stability in Healthy Adults

The Effect of a Novel Sock on Ankle Stability, Balance, and Muscle Contraction Time

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07812454
Acronym
Not provided
Enrollment
52
Registered
2026-09-10
Start date
2026-10-26
Completion date
2027-10-26
Last updated
2026-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postural Balance

Keywords

Ankle stability; dynamic balance; compression garments; muscle contraction; tensiomyography

Brief summary

This randomized study will compare a novel tensioning compression sock with a commercially available elastic foot and ankle compression sock in healthy adults. Participants will wear their assigned sock during waking hours for at least 6 hours per day for 7 days. Balance, ankle stability, grip strength, and tibialis anterior muscle contraction characteristics will be assessed at baseline and after the 7-day intervention. Participants will also report comfort and confidence in balance and stability after the intervention.

Detailed description

Participants will attend two in-person visits separated by 7 days. After consent, screening, and baseline testing, participants will be randomized using a computer-generated sequence concealed in sequentially numbered opaque envelopes. Participants will receive either the Trak Ground Wear C001 High-Performance Compression Sock or a commercially available elastic foot and ankle compression sock and will wear it for at least 6 hours per day during waking hours. Assessments include the Y-Balance Test, Side Hop Test, Biodex Balance System, handgrip dynamometry, and tensiomyography of the tibialis anterior. A post-intervention questionnaire will assess perceived comfort, balance confidence, stability, and willingness to wear the assigned sock.

Interventions

OTHERNovel Tensioning Compression Sock

Participants assigned to the control group will receive a commercially available elastic foot and ankle compression sock. Participants will be instructed to wear their assigned sock during waking hours for a minimum of 6 hours per day over the 7-day intervention period.

OTHERElastic Compression Sock

Participants assigned to the control group will receive a commercially available elastic foot and ankle compression sock. Participants will be instructed to wear their assigned sock during waking hours for a minimum of 6 hours per day over the 7-day intervention period.

Sponsors

University of Central Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants are assigned to one of two sock groups and remain in that group throughout the 7-day intervention period.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 18 years or older * Able to perform sit-to-stand, jumping, and single-leg standing without pain or discomfort * Able to read, write, and speak sufficient English to complete the study questionnaire * Shoe size within the study sock range: men's sizes 4-14 or women's sizes 6-13

Exclusion criteria

* Feelings of ankle instability * An ankle injury within the previous 12 months * Previous surgery on either lower extremity * History of torn ligaments or cartilage at the hip, knee, or ankle * Radicular symptoms in either lower extremity * Allergy to sock materials (80 percent nylon, 14 percent polyester, or 6 percent elastane) * Unable to consent * Pregnant * Prisoner

Design outcomes

Primary

MeasureTime frameDescription
Y-Balance Test7 daysMean Change From Baseline in Y-Balance Test Reach Distance at day 7 . Three recorded trials are completed in the anterior, posteromedial, and posterolateral directions on each limb and averaged.

Secondary

MeasureTime frameDescription
Side Hop Test7 daysChange From Baseline in Side Hop Test Score at day 7. Participants perform repeated single-leg side hops across lines 40 centimeters apart for 30 seconds; the highest of two trials is recorded.
Biodex Balance System7 daysMean Change From Baseline in Biodex Athlete Single Leg Stability Score at day 7. Three 20-second trials are completed on each lower extremity.
Grip Strength7 daysMean Change From Baseline in Handgrip Strength at Day 7. Two maximal contractions are performed with each hand; the highest value for each hand is recorded.
Tensiomyography7 daysMean Change From Baseline in Tibialis Anterior Contraction Time at Day 7. Two tensiomyography measurements are obtained for each limb and averaged.
Confidence Survey7 daysParticipant-Reported Comfort, Balance Confidence, Stability, and Willingness to Wear the Assigned Sock at Day 7.

Contacts

CONTACTWilliam J Hanney, PhD
william.j.hanney@gmail.com407-823-0217
PRINCIPAL_INVESTIGATORWilliam J Hanney, PhD

UCF

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 11, 2026