MedPath

Kinesotaping and Strengthening Exercises in Treatment of Osgood-Schlatter Disease

Not Applicable
Not yet recruiting
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
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
  1. History of low back pain.
  2. Trauma to the knee joint.
  3. Loss of joint play in tibiofemoral and patellofemoral articulations.
  4. Lower extremity fracture and surgery.
  5. Neurological deficit or movement disorder.
  6. If they had meniscal symptoms.
  7. If they had rheumatoid.
  8. If they had osteoarthritis.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in muscle strengthat first week and after 6 weeks of treatment

Quadriceps muscle strength will be assessed by hand held dynamo-meter.

Secondary Outcome Measures
NameTimeMethod
Change in Pain levelat first week and after 6 weeks of treatment

Pain threshold will be assessed by visual analogue scale

Change in functional disabilityat first week and after 6 weeks of treatment

Functional disability will assessed by lower extremity functional scale

Knee joint range of motionat 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.

© Copyright 2025. All Rights Reserved by MedPath