- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06295198
The Effect of Different Talocrural Joint Mobilization Techniques in Lateral Ankle Sprain
Investigation of the Effects of Different Talocrural Mobilization Techniques on Jumping Performance and Kinesiophobia in Professional Basketball Players With Lateral Ankle Sprain -Randomized Single-Blind Study
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul
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Besiktas, Istanbul, Turkey, 34353
- Bahcesehir university
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
18-35 years old Being a professional basketball player Clinical diagnosis of lateral ankle sprain in the last 12 months Having a Cumberland Ankle Instability Test score <24 >2.5 cm symmetry between the two extremities in the lunge test Not to participate in any ankle treatment program in the last three months, Being Volunteer
Exclusion Criteria:
History of lower extremity surgery History of disease that may affect sensorimotor function in the lower extremity Musculoskeletal disorders that may affect balance Having any musculoskeletal and orthopedic problems Having a history of previous ankle fracture or ankle surgery Presence of any visual impairment, metabolic, neurological or rheumatological disease
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: Mulligan Group
Participants in the Mulligan group stood in front of the physical therapist at the end of the treatment table and placed their affected lower extremity forward and the other slightly backward.
The physical therapist placed both hands on top of each other on the patient's talus to stabilize the talus.
The athlete was asked to move until he reached the end of his pain-free ankle dorsiflexion range.
Meanwhile, the physiotherapist gave posterior pushing with both hands.
The Mulligan mobilization technique was performed 10 times by each athlete.
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All evaluations will be repeated before and after the treatment.
Other Names:
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Experimental: Maitland Group
Maitland group, III.
degree talus mobilization technique was applied.
In this mobilization technique, 120 seconds of application, 60 seconds of rest, and then 120 seconds of application were performed.
Maitland III, which takes 5 minutes in total.
For the 10-degree mobilization technique, the participant was placed on his back with the foot pointing forward, the ankle was placed in 20° plantar flexion, and the talocrural ligament was in a relaxed position.
The hand stabilizing the foot was placed proximal to the malleolus to stabilize the leg.
The other hand performing the mobilization grasped the anterior talus using the first web space.
The talus was then shifted posteriorly downwards with force.
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All evaluations will be repeated before and after the treatment.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Single-leg drop jump test
Time Frame: baseline, immediately after the intervention
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Upon instruction, participants will aim to fall to the ground with the leg to be tested from the 30 cm high step, with their hands on their hips, and then immediately jump as high as possible.
Specific instructions are given as "minimizing ground contact time and maximizing bounce height," in line with previous research.
A one-minute rest is allowed between attempts.
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baseline, immediately after the intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight-bearing lunge test
Time Frame: baseline, immediately after the intervention
|
Weight-bearing lunge test (WBLT) is frequently used in individuals with ankle instability in order to determine dorsiflexion normal joint movement.
During WBLT the participant puts their hands on the wall and takes one leg forward and the other leg helps balance behind.
The maximum distance that the knee touches the wall is recorded without allowing the heel of the front foot to lose contact with the ground.
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baseline, immediately after the intervention
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Tampa kinesiophobia scale
Time Frame: baseline, immediately after the intervention
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The Tampa kinesiophobia (TKS) scale is often used in musculoskeletal injuries.
TKS has a checklist of 17 questions.
A 4-point Likert scoring (1= I strongly disagree, 4= I totally agree) is used in the scale.
After reversing items 4, 8, 12 and 16, a total score is calculated.
The person gets a total score between 17-68.
A high score on the scale indicates a high level of kinesiophobia.
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baseline, immediately after the intervention
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Fear Avoidance Belief Questionnaire
Time Frame: baseline, immediately after the intervention
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The Fear Avoidance Questionnaire is a 10-item instrument designed to measure fear avoidance related to injury in sports.
All items have a Likert type scale (1-5) from "strongly disagree" to "strongly agree" to be scored.
The FAQ score ranges from 10 to 50.
A higher score indicates a higher level of fear related to sports injury.
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baseline, immediately after the intervention
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Pelin Pişirici, PT, PhD, Bahcesehir University, Faculty of Health Sciences, Department of Physiotherapy
- Principal Investigator: Arif Ozan Yıldırım, PT, MSc, Bahcesehir University, Graduate Education Institute
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- OPMM-Ankle Instability
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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