Effects of Pilates Training on Ankle Proprioception, Postural Control and Performance in Footballers With Chronic Ankle Instability (CAI)

This study aims to contribute to the effects of Pilates training on ankle proprioception, postural control, and performance in football players with chronic ankle instability. Eighty eight participants will be randomly allocated into two groups and will receive both Pilates and balance training for eight weeks. it is hypothesized that the group that will receive Pilates taring will produce greater improvements as compared to other group.

Study Overview

Detailed Description

Chronic ankle instability is a frequently encountered issue in footballers, characterized by repeated episodes of the ankle "giving way," resulting in functional limitations and increased risk of future injuries. Conventional rehabilitation protocols often fail to restore optimal neuromuscular control, particularly proprioceptive and postural capabilities. Given the demands of football, this deficit can significantly hinder athletic performance and increase injury susceptibility. While Pilates-based rehabilitation has shown promise in improving core strength, balance, and neuromuscular coordination, there is a paucity of research examining its role in the context of CAI. This study addresses this research gap by assessing the effectiveness of Pilates training in improving key functional deficits among footballers with CAI, potentially informing more effective and sport-specific rehabilitation strategies.

Participants will be randomized into two groups:

  1. Pilates Training Group
  2. Control Group Intervention The intervention will last [insert duration 8 weeks], with participants attending three supervised sessions per week. Each session will last 60 minutes and will be led by a qualified physical therapist experienced in Pilates and sports rehabilitation.

After the intervention period, post-intervention assessments using the same outcome tools will be conducted by the same blinded assessor under identical conditions to the baseline evaluation. Any adverse events or dropouts will be recorded throughout the study.

Group A: Pilates Intervention Group Duration: 8 weeks (3 sessions/week) Session Duration: 60 minutes per session Equipment Used: Yoga mat, resistance bands, Pilates ring, small stability ball, foam roller.

Structure of Each Session:

Phase Time Activities Warm-Up 10 min Gentle dynamic stretches and mobility exercises (e.g., neck rolls, shoulder circles, hip openers, ankle circles) Core Pilates Training 40 min - Beginner-Intermediate Mat Pilates targeting core, hips, gluts, and lower leg muscles - Sample Exercises: - Pelvic tilts - Hundred - Single-leg stretch - Shoulder bridge with ankle engagement - Side-lying leg circles - Toe taps and leg lifts with ankle focus Cool Down 10 min Static stretching, deep breathing, and relaxation techniques

Progression:

Exercises will be progressed weekly by:

  • Increasing repetitions and sets
  • Reducing support (e.g., double leg to single leg)
  • Incorporating dynamic and unstable surfaces (foam pads, balance discs) Group B: Control Group Duration: 8 weeks (3 sessions/week) Session Duration: 60 minutes per session Equipment Used: Balance board, wobble disc, cones, foam pads, resistance bands.

Structure of Each Session:

Phase Time Activities Warm-Up 10 min Light jogging, ankle mobility drills, dynamic stretching Balance Training 40 min - Static and Dynamic Balance Drills: - Single-leg stance (eyes open/closed) - Wobble board balancing - Star excursion balance test practice - Tandem walking on a line - Forward/backward hops on one leg - Cone drills with reach tasks and steps up Cool Down 10 min Ankle and lower limb stretching, breathing techniques

Progression:

  • Decrease base of support
  • Introduce perturbations (e.g., partner tapping)
  • Dual-task activities (catching, counting, etc.)

Study Type

Interventional

Enrollment (Estimated)

88

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

Male footballers aged 22-35

  • History of unilateral ankle sprain in past 12 months
  • Inability to bear weight post-injury
  • CAIT score < 24
  • Minimum of 1-year experience in football

Exclusion Criteria:

  • Bilateral ankle sprains
  • Lower limb fractures or surgeries
  • Neurological conditions (e.g., MS, CMT, Stroke)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group A
Pilates training group

Duration: 8 weeks (3 sessions/week) Session Duration: 60 minutes per session Equipment Used: Yoga mat, resistance bands, Pilates ring, small stability ball, foam roller.

Structure of Each Session:

Phase Time Activities Warm-Up 10 min Gentle dynamic stretches and mobility exercises (e.g., neck rolls, shoulder circles, hip openers, ankle circles) Core Pilates Training 40 min - Beginner-Intermediate Mat Pilates targeting core, hips, gluts, and lower leg muscles - Sample Exercises: - Pelvic tilts - Hundred - Single-leg stretch - Shoulder bridge with ankle engagement - Side-lying leg circles - Toe taps and leg lifts with ankle focus Cool Down 10 min Static stretching, deep breathing, and relaxation techniques

Progression:

Exercises will be progressed weekly by:

  • Increasing repetitions and sets
  • Reducing support (e.g., double leg to single leg)
  • Incorporating dynamic and unstable surfaces (foam pads, balance discs)
Experimental: Group B
Balance training group

Group B: Control Group Duration: 8 weeks (3 sessions/week) Session Duration: 60 minutes per session Equipment Used: Balance board, wobble disc, cones, foam pads, resistance bands.

Structure of Each Session:

Phase Time Activities Warm-Up 10 min Light jogging, ankle mobility drills, dynamic stretching Balance Training 40 min - Static and Dynamic Balance Drills: - Single-leg stance (eyes open/closed) - Wobble board balancing - Star excursion balance test practice - Tandem walking on a line - Forward/backward hops on one leg - Cone drills with reach tasks and steps up Cool Down 10 min Ankle and lower limb stretching, breathing techniques

Progression:

  • Decrease base of support
  • Introduce perturbations (e.g., partner tapping)
  • Dual-task activities (catching, counting, etc.)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postural control
Time Frame: Base line before intervention after 8 weeks post intervention
The YBT has the patient stand on one leg while reaching out in 3 different directions with the other lower extremity. They are anterior, posteromedial and posterolateral. When using the Y-Balance test kit, the 3 reaches yield a "composite reach distance" or composite score used to predict injury.
Base line before intervention after 8 weeks post intervention
ankle proprioception
Time Frame: Baseline: Before intervention 8 weeks post-intervention
The goniometer was used to measure the ankle proprioception. Testing was performed the way that the person would sit on a chair so that a 90-degree angle of thigh and knee was maintained, and the height of the chair was such that the soles of the individual could not reach the ground. Then the person's foot was positioned with the goniometer in such a way that the eyes of the person were closed. Then the individual foot was inactively taken to the midrange. This angle was 10 degrees for dorsiflexion, 20 degrees for plantar flexion, 15 degrees for inversion and 10 degrees for eversion. Afterwards, the person was asked to actively re-create the desired angle with his closed eye; the test was performed three times, and the mean of three times of the angle of reconstruction determined the individual's score in each of the state.
Baseline: Before intervention 8 weeks post-intervention
performance
Time Frame: base line before intervention and 8 weeks post intervention
The Foot and Ankle Ability Measure (FAAM) is a self-report outcome instrument developed to assess physical function for individuals with foot and ankle related impairments. This self-report outcome instrument is available in English, German, French and Persian. The Foot and Ankle Ability Measure is a 29-item questionnaire divided into two subscales: The Foot and Ankle Ability Measure, 21-item Activities of Daily Living Subscale and the Foot and Ankle Ability Measure, 8-item Sports Subscale. The Sports subscale assesses more difficult tasks that are essential to sport, it is a population-specific subscale designed for athletes.
base line before intervention and 8 weeks post intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Muhammad Tariq Shafi, Lahore University of Biological and Applied Sciences

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

November 25, 2025

Primary Completion (Estimated)

May 25, 2026

Study Completion (Estimated)

May 30, 2026

Study Registration Dates

First Submitted

November 24, 2025

First Submitted That Met QC Criteria

November 24, 2025

First Posted (Actual)

December 5, 2025

Study Record Updates

Last Update Posted (Actual)

December 5, 2025

Last Update Submitted That Met QC Criteria

November 24, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • UBAS/ERB/FoRS/25/020

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Performance

Clinical Trials on Pilates exercises

Subscribe