- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07427290
Effects of Combined Exercise and Kinesio Taping on Balance and Jump Performance in Athletes With Chronic Ankle Instability (NR-CAI)
Combined Neuromuscular Rehabilitation Enhances Static Balance in Athletes With Chronic Ankle Instability: A Randomized Controlled Trial
The goal of this clinical trial is to evaluate whether a combined neuromuscular rehabilitation program improves static balance in athletes with chronic ankle instability. It will also examine whether the addition of kinesio taping provides extra benefit compared with exercise alone. The main questions it aims to answer are:
Does a six-week balance and strength exercise program improve static postural control in athletes with chronic ankle instability?
Does adding kinesio taping to the exercise program lead to greater improvements in balance compared with exercise alone?
Researchers will compare three groups: an exercise group, an exercise plus kinesio taping group, and a control group, to determine which approach is most effective for improving balance.
Participants will:
Take part in a supervised rehabilitation program three times per week for six weeks (intervention groups)
Perform balance training on a wobble board and strength exercises using elastic resistance bands
Receive kinesio taping before each session if assigned to the taping group
Undergo balance assessments before and after the intervention using force-plate measurements
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Chronic ankle instability is a frequent condition among athletes and is associated with recurrent ankle sprains, impaired proprioception, muscle weakness, and deficits in postural control. These impairments negatively influence athletic performance and increase the risk of further injury. Neuromuscular rehabilitation programs that combine balance and strength training are commonly recommended to address these problems; however, evidence regarding the additional value of adjunctive interventions such as kinesio taping remains limited.
This randomized controlled trial was conducted to investigate the effectiveness of a structured neuromuscular rehabilitation program on static balance in athletes with chronic ankle instability and to determine whether the addition of kinesio taping enhances treatment outcomes. Participants meeting the diagnostic criteria for chronic ankle instability were recruited and randomly allocated into one of three study groups.
The intervention consisted of a supervised rehabilitation program focused on balance and strength exercises targeting the ankle joint. Training sessions were performed regularly over a six-week period. In one group, kinesio taping was applied before each training session in addition to the exercise program, while another group performed the same exercises without taping. A control group did not receive any specific rehabilitation intervention.
Balance performance was evaluated before and after the intervention period using objective laboratory-based assessments. The study design allowed for comparison of changes over time within each group and between groups in order to identify the most effective approach for improving postural stability in athletes with chronic ankle instability.
The findings of this trial are intended to provide practical clinical evidence for physiotherapists and sports rehabilitation professionals regarding optimal conservative management strategies for chronic ankle instability.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Tirana, Albania, 1001
- Sport University of Tirana
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria: History of at least one ankle sprain occurring at least 12 months prior to enrollment.
Presence of clinical signs of pain and inflammation. Most recent ankle sprain occurring at least 3 months before study inclusion. History of more than two episodes of "giving way". Self-reported ankle instability assessed using the Cumberland Ankle Instability Tool (CAIT) with a score of ≤25 points.
Exclusion Criteria:
History of musculoskeletal surgery. Presence of orthopedic conditions such as lower-limb fractures. Any musculoskeletal injury within the 3 months preceding the study. Known neurological disorders that could influence balance performance. Known vestibular disorders that could influence balance performance.
Study Plan
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: Combined Rehabilitation Group
Participants in this group received a combined rehabilitation program consisting of balance and strength exercises together with kinesio taping applied to the ankle.
The intervention was performed according to a standardized protocol for improving balance and ankle stability
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The same six-week balance and strength rehabilitation program as in the Exercise Group, combined with Kinesio Taping applied to the ankle before each training session.
Taping was applied by a certified physiotherapist using a standardized technique to enhance proprioceptive input and neuromuscular activation.
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|
Experimental: Exercise Only Group
Participants in this group received only the exercise program (balance and strength) without kinesio taping.
The exercises were identical to those used in the combined group and followed the same duration and frequency.
|
A structured rehabilitation program consisting of balance training on a wobble board and ankle strengthening exercises using Thera-Band.
Sessions were performed three times per week for six weeks under physiotherapist supervision.
Exercises included single-leg balance tasks with progressive difficulty and strengthening exercises targeting dorsiflexion, plantarflexion, inversion, and eversion.
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No Intervention: Control Group
Participants in this group did not receive any structured rehabilitation intervention during the study period.
They continued their usual daily activities without additional therapeutic exercises or kinesio taping.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Static Balance Measured by Center of Pressure Ellipse Area
Time Frame: From baseline assessment to post-intervention assessment after 6 weeks
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Static balance will be assessed using a force plate by analyzing center of pressure (COP) parameters, specifically the ellipse area.
Measurements will be performed in a single-leg stance position under two conditions: eyes open and eyes closed.
Smaller COP ellipse area values indicate better postural control.
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From baseline assessment to post-intervention assessment after 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vertical Jump Height
Time Frame: Baseline and post-intervention
|
Vertical jump height will be assessed using a force plate to quantify lower limb explosive power, measured at baseline and post-intervention.
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Baseline and post-intervention
|
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Drop Jump
Time Frame: Baseline and post-intervention
|
Drop jump performance will be assessed using a force plate to evaluate reactive strength and neuromuscular control, measured at baseline and post-intervention.
|
Baseline and post-intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CAI-RTC-2024-ALB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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