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Recruiting Not applicable

Acute Effect of Graded Motor Imagery on Ankle Rehabilitation: A Pilot Study

NCT07376915 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-02-09
Last updated
2026-02-11

Condition(s) studied

Ankle InstabilityHealthy Controls

Investigational drug(s) / intervention(s)

graded motor imagery

graded motor imagery: The Graded Motor Imagery (GMI) program will be applied six consecutive days nd will consist of three progressive stages: Laterality Training: Participants will perform right-left ankle discrimination tasks using validated foot and ankle images. Accuracy and response time will be recorded. Motor Imagery: Participants will mentally rehearse ankle movements such as dorsiflexion, plantarflexion, inversion, and eversion without performing the motion. Imagery tasks will progress from simple movements to functional patterns based on tolerance. Mirror Therapy: A mirror will be placed in the midsagittal plane, allowing participants to view the reflection of the non-affected ankle while performing movements. The visual illusion of normal movement is intended to improve motor control and proprioception.

Study summary

The primary aim of this study is to evaluate the immediate and short-term effects of the Graded Motor Imagery (GMI) method on individuals with chronic ankle instability (CAI). In this context, the effects of the Graded Motor Imagery intervention on pain level, muscle stiffness, muscle strength, functional performance, and subjective instability level will be investigated. Additionally, these effects will be comparatively analyzed with an age- and sex-matched control group consisting of healthy individuals.

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Aged between 18 and 40 years. * Diagnosed with chronic ankle instability (CAIT ≤ 24). * History of an acute ankle sprain occurring more than 3 months prior to enrollment. * Has not received ankle rehabilitation treatment. * Voluntarily participated in this study Exclusion Criteria: * Vestibular or neurological disorders * Other lower extremity injuries * History of surgery

Primary outcome measure(s)

  • Subjective Instability (CAIT) — baseline
    A valid-reliable questionnaire that questions the perceived instability in daily life and sports activities. Clinical Significance: ≥ 3 point increase is considered clinically significant
  • Subjective Instability (CAIT) — 1-week post-intervention
    A valid-reliable questionnaire that questions the perceived instability in daily life and sports activities. Clinical Significance: ≥ 3 point increase is considered clinically significant
  • Ground Reaction Force & Static Balance (ForceDecks) — baseline
    Device: ForceDecks dual force platform. 1. Single-Leg Jump Test\* Values: Net vertical ground reaction force (N·kg-¹), flight time (ms), asymmetry (%). 2. Single-Leg Static Balance\* Values: Total sway path (mm), ellipse area (mm²). Clinical Importance:\* Captures short-term changes in neuromuscular control and explosive strength in a detailed manner.
  • Ground Reaction Force & Static Balance (ForceDecks) — 1-week post-intervention
    Device: ForceDecks dual force platform. 1. Single-Leg Jump Test\* Values: Net vertical ground reaction force (N·kg-¹), flight time (ms), asymmetry (%). 2. Single-Leg Static Balance\* Values: Total sway path (mm), ellipse area (mm²). Clinical Importance:\* Captures short-term changes in neuromuscular control and explosive strength in a detailed manner.

Trial sites (1)

FacilityCityRegionStatus
İstanbul Üniversitesi-Cerrahpaşa Istanbul Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07376915 on ClinicalTrials.gov ↗ ← All trials in Turkey