Kinesotaping and Strengthening Exercises in Treatment of Osgood-Schlatter Disease
- Conditions
- Osgood-Schlatter Disease
- Registration Number
- NCT06993363
- Lead Sponsor
- Cairo University
- Brief Summary
The purpose of this study is to investigate the effect of adding kinesotaping to quadriceps strengthening exercises on muscle strength, pain, function and range of motion of knee joint in patients with Osgood-Schlatter disease (OSD).
- 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:
1. Quadriceps muscles strength will be assessed by hand held dynamotor.
2. Pain intensity will be measured by visual analog scale.
3. Disability function of knee will be measured by lower extremity functional scale (LEFS-Ar).
4. 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.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 60
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
- 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 & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change in muscle strength at first week and after 6 weeks of treatment Quadriceps muscle strength will be assessed by hand held dynamo-meter.
- Secondary Outcome Measures
Name Time Method Change in Pain level at first week and after 6 weeks of treatment Pain threshold will be assessed by visual analogue scale
Change in functional disability at first week and after 6 weeks of treatment Functional disability will assessed by lower extremity functional scale
Knee joint range of motion 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.