# Corticomotor Excitability Changes Induced by Progressive Balance Exercises in Chronic Ankle Instability: a Randomized Clinical Trial

**Authors:** Mahdis Purzolfi, Cyrus Taghizadeh Delkhoush, Majid Mirmohammadkhani

PMC · DOI: 10.1002/brb3.71222 · 2026-01-29

## TL;DR

A 6-week balance exercise program increased brain-to-muscle signaling in people with chronic ankle instability, suggesting improved neural control.

## Contribution

This study demonstrates that progressive balance exercises can enhance corticomotor excitability in individuals with chronic ankle instability.

## Key findings

- Corticomotor thresholds and cortical silent period of the peroneus longus muscle decreased significantly after 6 weeks of progressive balance exercises.
- Normalized motor evoked potential of the peroneus longus muscle increased significantly following the exercise intervention.
- There was a significant interaction effect between groups for corticomotor excitability measures, indicating a stronger response in the intervention group.

## Abstract

Progressive balance exercises may change corticomotor excitability during the learning process of postural stability control. The primary purpose of the present study was to assess corticomotor excitability corresponding to the peroneus longus muscle under transcranial magnetic stimulation following 6 weeks of progressive balance exercises in individuals with chronic ankle instability.

Eligible volunteers diagnosed with chronic ankle instability were randomly assigned to either the intervention group or the control group. The intervention group practiced progressive balance exercises every other day for 6 weeks, while the control group continued their daily activities. The corticomotor excitability outcome measures included the active and resting corticomotor thresholds, the motor evoked potential, and the cortical silent period of the peroneus longus muscle, which were measured using an electromyography device under a transcranial magnetic stimulator. The outcome measures were measured in the intervention group before and after progressive balance exercises, and in the control group at baseline and again after a 6‐week interval.

The corticomotor thresholds and cortical silent period of the peroneus longus muscle were significantly decreased within groups (p‐values < 0.001; η
2
p > 0.580). In addition, the normalized motor evoked potential of the peroneus longus muscle exhibited a significant increase within groups (p‐value < 0.001; η
2
p = 0.265). Interestingly, a significant interaction effect was revealed between the within‐group and between‐group effects for the corticomotor excitability outcome measures related to the peroneus longus muscle (p‐values < 0.001; η
2
p > 0.311).

Six weeks of progressive balance exercises significantly increased corticomotor excitability corresponding to the peroneus longus muscle in individuals with chronic ankle instability.

Corticomotor excitability changes induced by progressive balance exercises in chronic ankle instability: A randomized clinical trial.

## Full-text entities

- **Diseases:** psychiatric disorders (MESH:D001523), migraines (MESH:D008881), proprioceptive (MESH:D020886), musculoskeletal disorders (MESH:D009140), Stroke (MESH:D020521), vestibular or visual disturbances (MESH:D014786), neurological diseases (MESH:D020271), muscular dysfunction (MESH:D009135), subcutaneous hemorrhage (MESH:D006470), drug or alcohol addiction (MESH:D019966), intracranial malignancy (MESH:D009369), intracranial hypertension (MESH:D019586), seizures (MESH:D012640), muscle fatigue (MESH:D005221), neuromuscular disorder (MESH:D009468), swelling (MESH:D004487), cardiovascular diseases (MESH:D002318), injuries (MESH:D014947), Neurological Disorders (MESH:D009461), CAI (MESH:D016512), balance disorders (MESH:D009358), chronic (MESH:D002908), impairments (MESH:D060825), rheumatologic diseases (MESH:D012216), systemic diseases (MESH:D034721), pain (MESH:D010146)
- **Chemicals:** AgCl (MESH:C037548), Ionta (-), gamma-aminobutyric acid (MESH:D005680), caffeine (MESH:D002110), alcohol (MESH:D000438), Ag (MESH:D012834)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12856227/full.md

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Source: https://tomesphere.com/paper/PMC12856227