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NCT Number: NCT07273097

Effects of Ankle Evertor Fatigue on Perturbed Gait

This study will investigate the effects of ankle evertor muscle fatigue on gait stability during treadmill walking with mechanical perturbations. Participants will walk at two speeds (0.4 m/s and 1.0 m/s) while random medial and lateral perturbations (<10% body weight) are applied to the pelvis. Surface EMG from ankle muscles and center of pressure (COP)-based gait parameters (e.g., step length, step width, single support duration, COP trajectory) will be analyzed before and immediately after an isotonic fatigue protocol of the ankle evertors.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Rehabilitation Institute Republic of Slovenia - URI Soča

Ljubljana, 1000, Slovenia

Location status: Recruiting

Location contact

Urška Puh, PhD, PT, Assoc. Prof

CONTACT

[email protected]

+38640577131

About this study

The purpose of this study is to examine how ankle evertor muscle fatigue affects gait stability and neuromuscular responses during treadmill walking with mechanical perturbations. Perturbations will be applied randomly in the medial or lateral direction, but always shortly after initial foot contact, to specifically challenge ankle stabilization in stance.

The study will include individuals with chronic ankle instability (CAI) and matched healthy controls. In the CAI group, the symptomatic side will be targeted with the fatigue protocol, whereas in healthy controls the tested side will be assigned to match the distribution of sprain laterality in the CAI group.

Walking and perturbation protocol:

Participants will first complete familiarization at 1.0 m/s, including both normal and perturbed walking. After familiarization, the measurements will consist of 2 minutes of unperturbed walking followed by 3 minutes of perturbed walking. The same procedure will then be repeated at 0.4 m/s, with familiarization (normal and perturbed walking) preceding the measurement block.

The fatigue protocol will be applied immediately after these baseline blocks. Following fatigue, participants will immediately perform perturbed walking at 1.0 m/s. The fatigue protocol will then be repeated, followed by perturbed walking at 0.4 m/s.

Fatigue protocol:

Ankle evertor muscles will be fatigued using elastic resistance bands through repeated concentric and eccentric eversion contractions. The task will be paced using a metronome at a rate of one repetition per second, and will continue until the active eversion range of motion decreases by 50% compared to baseline.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for the healthy control group (no CAI):

  • Age between 18 and 45 years,
  • No history of injuries or surgical procedures to the lower limbs,
  • No peripheral or central neurological impairments.

Inclusion criteria

for the chronic ankle instability (CAI) group:

  • Age between 18 and 45 years,
  • No history of major surgical procedures on the lower limbs
  • No peripheral or central neurological impairments,
  • Diagnosed chronic ankle instability:
  • First ankle sprain occurred at least one year prior to testing,
  • At least three months since the most recent ankle sprain,
  • Subjective feeling of ankle instability - CAIT (Cumberland Ankle Instability Tool) score < 24.

Exclusion criteria

for the CAI group:

  • Other pathologies of the ankle joint.
  • Acute pain

Treatment and study plan

muscle fatigue

Other

The fatigue protocol will consist of repeated concentric-eccentric ankle eversion contractions against elastic resistance at a pace of one repetition per second, guided by a metronome, and performed in a seated position. Fatigue will be defined as a clear inability to perform the full range of eversion, i.e. the range of motion falling below 50% of the initial value despite evident effort by the participant.

Primary outcomes

  1. Surface EMG root mean square (RMS) amplitude of ankle muscles

    Time frame: Baseline (Day 1, prior to fatigue protocol) and immediately post-fatigue (Day 1, within 5 minutes after fatigue protocol).

    Surface EMG RMS amplitude from peroneus longus (PL), tibialis anterior (TA), soleus (SOL), gastrocnemius medialis (GM), and gluteus medius (GMed), recorded bilaterally during treadmill walking. EMG will be time-normalized to the gait cycle (0-100%). The primary epoch is the perturbation step (shortly after initial contact through stance). For each muscle and speed, EMG during perturbed walking will be normalized to matched unperturbed walking.

  2. Center of Pressure mediolateral displacement (COPx)

    Time frame: Baseline (Day 1, prior to fatigue protocol) and immediately post-fatigue (Day 1, within 5 minutes after fatigue protocol).

    Mediolateral displacement of the center of pressure (COPx) during walking, time-normalized to the gait cycle (0-100%). In addition, COPx will be expressed relative to the sacral marker (COPx-SACRx). Values will be presented in absolute units (cm) and compared between matched perturbed steps at the same walking speed (before and after fatigue).

Secondary outcomes

  1. Step Length and width

    Time frame: Baseline (Day 1, prior to fatigue protocol) and immediately post-fatigue (Day 1, within 5 minutes after fatigue protocol).

    Step length (heel-to-heel) and step width of the perturbation step, derived from 3D motion capture with reflective markers placed on anatomical landmarks. Both parameters will be compared against matched unperturbed steps.

  2. Ground reaction forces (GRF)

    Time frame: Baseline (Day 1, prior to fatigue protocol) and immediately post-fatigue (Day 1, within 5 minutes after fatigue protocol).

    Vertical GRF (Fz; peak, mean, loading rate), with optional analysis of anteroposterior (Fy) and mediolateral (Fx) components, time-normalized to the gait cycle (0-100%). Values reported in absolute units (N for forces; N/s for loading rate).

  3. Ratings of perceived exertion

    Time frame: Baseline (Day 1, prior to fatigue protocol) and immediately post-fatigue (Day 1, within 5 minutes after fatigue protocol).

    Description: Ratings of perceived exertion (RPE) will be assessed at the end of each fatigue protocol using the Borg 10 category-ratio scale, with 0 is no effort and 10 is an extreme physical effort.

Study contacts

Contact information is provided by the study sponsor or research team.

Alan Kacin, PhD, PT, Prof

CONTACT

[email protected]

+38613001119

Tjaž Brezovar

CONTACT

[email protected]

+38640777919

Sponsors and collaborators

Lead sponsor

University of Ljubljana

Other

Registry information

Official study title

Effects of Ankle Evertor Fatigue on Gait Perturbation Responses in Individuals With and Without Chronic Ankle Instability

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 9, 2025
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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