Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 7:56 PM
Ignite Modification Date:
2025-12-24 @ 7:56 PM
NCT ID:
NCT04503304
Brief Summary:
This study will try to answer the following question:
Would strengthening of hip abductors be equal to, or more effective than, knee extensors strengthening in improving pain, function and knee extensors isometric strength in patients with knee Osteoarthritis
Detailed Description:
A total of 70 patients with knee Osteoarthritis will be recruited All patients who will participate in the study will be referred by orthopedists. Patients with knee osteoarthritis will be included with age ranges from 50-70. They will be randomized into 2 groups; hip abductors strengthening (HAS) group a will receive hip abductors strengthening exercises, and knee extensors strengthening (KES) group will receive quadriceps strengthening exercise.
All patients who will meet the study criteria will get a complete knowledge of the objectives and procedures of the study.
Inclusion criteria:
1. Patients with knee Osteoarthritis grade II- III Kellgren- Lawrence scores
2. Their age is 50-70\[Wang et al.,2019\].
3. Body mass index (BMI) 25-30.
Exclusion criteria:
1. Patients who had surgical intervention in the knee and/or hip.
2. Fracture in the lower limbs.
3. Malignancy
4. Any associated ligamentous injuries in knee or ankle.
5. Spinal Cord Injury.
6. Hormonal imbalance or on hormonal therapy
7. Knee injection within the last 6 months prior to the study. Outcome parameters including Quadriceps Muscle Strength, the arabic version of Western Ontario and McMaster Universities Arthritis Index questionnaire total score and 3 subscales and Timed Up and Go test score
Study:
NCT04503304
Study Brief:
Protocol Section:
NCT04503304