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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Central Florida

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Novel Tensioning Compression Sock

    Other intervention

    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.

  • Elastic Compression Sock

    Other intervention

    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.

Treatment groups

52 Participants
are divided into 2 treatment groups
Group A: Novel Tensioning Compression SockExperimental treatment 1 intervention
Group B: Elastic Compression SockActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Y-Balance Test

Mean 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.

Time frame
7 days

Secondary outcomes

1

Side Hop Test

Change 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.

Time frame
7 days
2

Biodex Balance System

Mean Change From Baseline in Biodex Athlete Single Leg Stability Score at day 7. Three 20-second trials are completed on each lower extremity.

Time frame
7 days
3

Grip Strength

Mean 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.

Time frame
7 days
4

Tensiomyography

Mean Change From Baseline in Tibialis Anterior Contraction Time at Day 7. Two tensiomyography measurements are obtained for each limb and averaged.

Time frame
7 days

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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