- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07584746
Lower Extremity Mobility for CAI
Effects of Targeted Mobility Interventions at the Ankle Versus Hip on Clinical and Functional Outcomes in Chronic Ankle Instability
This study will be conducted to determine the effect of addition of ankle mobility versus hip mobility exercises to traditional rehabilitation to patients with chronic ankle instability. the main purpose is to answer the following question:
- out of these interventions which would better improve lower limb flexibility, range of motion, severity of functional instability and dynamic postural control?
Researcher will compare between ankle mobility versus hip mobility exercises
Participants will be allocated in 2 experimental groups:
- group A will include 20 patients receiving conventional physiotherapy in addition to ankle mobility exercises
- group B will include 20 patients receiving conventional physiotherapy in addition to hip mobility exercises
Patients will receive 3 sessions per week for 6 weeks in a physiotherapy outpatient facility for both groups
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Amal Mounir Mohamed
- Phone Number: +201141099494
- Email: amalmunir26@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adults (18-30 years old) with chronic ankle instability
- Patient's Body mass index (BMI) will range from 18.5- 29.9 kg/m2
- A history of at least one ankle sprain with the initial sprain occurring 12 months prior to study
- Most recent injury 3 months prior to start of treatment with at least one day of interrupted desired physical activity and associated inflammatory symptoms (pain, swelling, etc.).
- A history of previous giving way and/or recurrent sprain, and/or feeling of instability to injured ankle.
- Cumberland Ankle Instability Tool: score of ≤ 24.
Exclusion Criteria:
- Other lower extremity injury surgery 6 months before testing
- Patient suffered an acute sprain in the previous 6 weeks to the start of the study.
- History of neuromuscular disorders.
- Systemic diseases that affect balance.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A
20 patients (10 males and 10 females) will receive ankle mobility exercises and traditional physiotherapy program
|
9 ankle mobility exercises including: ankle pumps, ankle circles, forward lunges, plantarflexion stretch, calf stretch, squat with overhead reach, heel drops on step, ankle flexion with band and scoops
|
|
Experimental: Group B
20 patients (10 males and 10 females) will receive hip mobility exercises and traditional physiotherapy program
|
8 hip mobility exercises including: 90/90 hip stretch, frog stretch, world's greatest stretch, banded hamstring stretch, backward lunges, butterfly, pigeon stretch and banded hip stretch.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
lower limb flexibility
Time Frame: 6 weeks
|
measure the lower trunk and lower extremity flexibility with modified sit and reach test, sideways split and single legged knee bend test
|
6 weeks
|
|
Range of motion
Time Frame: 6 weeks
|
Hip flexion and extension range of motion Ankle dorsiflexion and plantarflexion range of motion
|
6 weeks
|
|
Dynamic postural control
Time Frame: 6 weeks
|
using the modified star excursion balance test
|
6 weeks
|
|
severity of chronic ankle instability
Time Frame: 6 weeks
|
using the Arabic version of the Cumberland Ankle Instability Tool, a tool used to describe the severity of chronic ankle instability, with the highest possible score is: 30 and the lowest possible score is: 0 Higher scores indicate better ankle stability, while lower scores indicate higher severity of functional instability
|
6 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- Mobility training for CAI
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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