- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06993363
- Original Trial
Kinesotaping and Strengthening Exercises in Treatment of Osgood-Schlatter Disease
Effect of Adding Kinesotaping to Quadriceps Strengthening on Knee Function in Patients With Osgood Schlatter
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
60 patients will be participated in this study. The patients of both genders with age ranges from 18 -25 years old. The sample will randomly be divided into two groups.
Group A: will receive strengthening exercise for quadriceps muscle and stretching exercises for hamstring and calf muscles Group B: will receive kinesoatping, strengthening exercises for quadriceps muscle and stretching exercises for hamstring and calf muscles .
All subject will receive the treatment for 6 weeks, All subjects will assign consent form before starting this study and will be explained the purpose of this study before any application.
Outcome measurements:
- Quadriceps muscles strength will be assessed by hand held dynamotor.
- Pain intensity will be measured by visual analog scale.
- Disability function of knee will be measured by lower extremity functional scale (LEFS-Ar).
- Range of motion of knee joint will be measured by smart phone application for range of motion measurement.
Data will be collected prior to first session as pre-test measure and at the end of last treatment session as post-test treatment.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Cairo, Egypt
- Physical therapy College - Cairo university
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
1 - Age - 18 years to 25 years 2. Knee Osgood schlatter disease as per diagnosed by orthopaedisit 3. Duration of knee pain is 4-5 weeks during 6 months prior to study. 4- patients from both gender 5- BMI from 18 Kg/M2 to 25 Kg/M2
Exclusion Criteria:
- History of low back pain.
- Trauma to the knee joint.
- Loss of joint play in tibiofemoral and patellofemoral articulations.
- Lower extremity fracture and surgery.
- Neurological deficit or movement disorder.
- If they had meniscal symptoms.
- If they had rheumatoid.
- If they had osteoarthritis.
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 |
|---|---|
|
Active Comparator: Group A
Patients will receive strengthening exercises to quadriceps muscle and stretching exercises to hamstring and calf muscles
|
Static Quad Pull the toes up towards your shin, push your knee into the bed to tighten the quad muscles. This should cause your heel to slightly lift off the bed. Hold for 7 seconds. Repeat on affected leg. Straight leg raising
Hamstring stretching exercise will be done in the long sitting position. The patient will be instructed to keep his affected knee always extended while folding the other leg to the side then he will bend his trunk forward as much as he could in order to touch his toes by his fingers. Calf muscle stretching: The patient will be positioned in the long-sitting with the knees extended. The patient will be instructed to pull his foot into dorsiflexion as much as he could with the assistance of a rolled towel holding this position for 30 seconds (Fig14). The patient will then be instructed to go back to starting position and relax for 30 seconds. This exercise will be done 5 times per session. |
|
Experimental: Group B
Patients will receive kinesotaping, strengthening exercises to quadriceps muscle and stretching exercises to hamstring and calf muscles
|
Static Quad Pull the toes up towards your shin, push your knee into the bed to tighten the quad muscles. This should cause your heel to slightly lift off the bed. Hold for 7 seconds. Repeat on affected leg. Straight leg raising
Hamstring stretching exercise will be done in the long sitting position. The patient will be instructed to keep his affected knee always extended while folding the other leg to the side then he will bend his trunk forward as much as he could in order to touch his toes by his fingers. Calf muscle stretching: The patient will be positioned in the long-sitting with the knees extended. The patient will be instructed to pull his foot into dorsiflexion as much as he could with the assistance of a rolled towel holding this position for 30 seconds (Fig14). The patient will then be instructed to go back to starting position and relax for 30 seconds. This exercise will be done 5 times per session. 1 full 25cm strip of KT Tape cut in half. Apply one hour before beginning activity. Clean dirt, oils and lotions from area. After application rub tape vigorously to activate adhesive. Bend the knee at a 90 degree angle Anchor the middle of a half strip of tape diagonally over the point of pain with 80% stretch. Apply ends of tape without stretch. Anchor the middle of a second half strip across the first strip to form an X pattern over the point of pain with 80% stretch. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in muscle strength
Time Frame: at first week and after 6 weeks of treatment
|
Quadriceps muscle strength will be assessed by hand held dynamo-meter.
|
at first week and after 6 weeks of treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Pain level
Time Frame: at first week and after 6 weeks of treatment
|
Pain threshold will be assessed by visual analogue scale
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at first week and after 6 weeks of treatment
|
|
Change in functional disability
Time Frame: at first week and after 6 weeks of treatment
|
Functional disability will assessed by lower extremity functional scale
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at first week and after 6 weeks of treatment
|
|
Knee joint range of motion
Time Frame: at first week and after 6 weeks of treatment
|
11. Knee range of motion (flexion, extension) will be assessed by smart phone application (Doctor Goniometer) for range of motion measurement.
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at first week and after 6 weeks of treatment
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Neveen Abdelatif Professor of physical therapy - Cairo University, Professor, Department of Basic sciences for physical therapy, Faculty of Physical Therapy , Cairo university, Cairo, Egypt
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
- P.T.REC/012/005847
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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