NCT07812454

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
12mo left

Started Oct 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 3, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 10, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

October 26, 2026

Expected
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 26, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 26, 2027

Last Updated

September 10, 2026

Status Verified

September 1, 2026

Enrollment Period

1 year

First QC Date

September 3, 2026

Last Update Submit

September 3, 2026

Conditions

Keywords

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

Outcome Measures

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.

    7 days

Secondary Outcomes (5)

  • Side Hop Test

    7 days

  • Biodex Balance System

    7 days

  • Grip Strength

    7 days

  • Tensiomyography

    7 days

  • Confidence Survey

    7 days

Study Arms (2)

Novel Tensioning Compression Sock

EXPERIMENTAL

Participants wear the Trak Ground Wear C001 High-Performance Compression Sock during waking hours for at least 6 hours per day for 7 days.

Other: Novel Tensioning Compression Sock

Elastic Compression Sock

ACTIVE COMPARATOR

Participants wear a commercially available elastic foot and ankle compression sock during waking hours for at least 6 hours per day for 7 days.

Other: Elastic Compression Sock

Interventions

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.

Novel 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.

Elastic Compression Sock

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (4)

  • Tashiro T, Maeda N, Sasadai J, Kotoshiba S, Sakai S, Suzuki Y, Fujishita H, Urabe Y. Tensiomyographic Neuromuscular Response of the Peroneus Longus and Tibialis Anterior with Chronic Ankle Instability. Healthcare (Basel). 2021 Jun 10;9(6):707. doi: 10.3390/healthcare9060707.

    PMID: 34200684BACKGROUND
  • Ditroilo M, Smith IJ, Fairweather MM, Hunter AM. Long-term stability of tensiomyography measured under different muscle conditions. J Electromyogr Kinesiol. 2013 Jun;23(3):558-63. doi: 10.1016/j.jelekin.2013.01.014. Epub 2013 Feb 23.

    PMID: 23461833BACKGROUND
  • Harry-Leite P, Paquete M, Parada T, Fraiz JA, Ribeiro F. Kinesiology taping improves balance in football players with chronic ankle instability. J Bodyw Mov Ther. 2024 Oct;40:455-460. doi: 10.1016/j.jbmt.2024.04.048. Epub 2024 Apr 23.

    PMID: 39593625BACKGROUND
  • Alawna M, Mohamed AA. Short-term and long-term effects of ankle joint taping and bandaging on balance, proprioception and vertical jump among volleyball players with chronic ankle instability. Phys Ther Sport. 2020 Nov;46:145-154. doi: 10.1016/j.ptsp.2020.08.015. Epub 2020 Aug 29.

    PMID: 32937273BACKGROUND

Study Officials

  • William J Hanney, PhD

    UCF

    PRINCIPAL INVESTIGATOR

Central Study Contacts

William J Hanney, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants are assigned to one of two sock groups and remain in that group throughout the 7-day intervention period.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

September 3, 2026

First Posted

September 10, 2026

Study Start (Estimated)

October 26, 2026

Primary Completion (Estimated)

October 26, 2027

Study Completion (Estimated)

October 26, 2027

Last Updated

September 10, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared outside the research team. Results will be reported only in aggregate.