Adding Deep Front Line Myofascial Release to Selected Exercises in Patients With Knee Osteoarthritis

Not Applicable

Completed

• Conditions: Knee Osteoarthritis

• Registration Number: NCT05812898
• Lead Sponsor: Cairo University

Brief Summary

the aim of the study is to investigate the effect of deep front line myofascial release to selected exercises in patients with knee osteoarthritis

Detailed Description

: Knee osteoarthritis (KOA) also known as degenerative joint disease, is typically the result of wear and tear and progressive loss of articular cartilage.

The myofascial meridian is a new approach to the facial restriction .the knee capsules, the adductor muscles and the tipialis posterior are part of the deep front line which is a line of the myofascial meridian.

Exercise is the highest evidence in the treatment of knee osteoarthritis. The myofascial release is effective in the treatment of knee osteoarthritis so the study will investigate the effect of adding deep front line myofascial release to selected exercises in patients with knee osteoarthritis.

Study Timeline

• Study Start: 2023-01-01
• Primary Completion: 2023-04-01
• Study First Submitted: 2023-04-01
• Study First Submitted QC: 2023-04-01
• Study First Posted: 2023-04-14
• Study Completion: 2023-05-15
• Status Verified: 2024-02
• Last Update Submitted: 2024-02-05
• Last Update Posted: 2024-02-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

• Mild to moderate unilateral or bilateral medial tibiofemoral OA grade II-III (K/L).
• The age of the participants will range from 45 to 60 years old .
• BMI ranged from 20-30 kg/m2

Exclusion Criteria

1. Severe knee OA (grade IV according to K/L classification).
2. Congenital or acquired inflammatory, rheumatic or neurological (systemic or local) diseases involving the knee.
3. Patients receiving oral or injected corticosteroids for the last 3 months .
4. History of knee surgery/fracture.
5. Patients with ACL and meniscus injury

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
pain intensity	up to four weeks	The scale that will be used the visual analogue scale;each subject will instructed to record pain intensity on line of 100mm. Starting from no pain on the leftto the most sever pain imaginable on the right Patient will choose the point which describe his pain.the more the score toward the end the more severe pain
rang of motion	up to four weeks	using digital inclinometer
function	up to four weeks	The Arabic version of reduced Western Ontario and McMasters University Osteoarthritis Index (ArWOMAC) index will be used to measure functional disability.is a self-administered questionnaire consisting of 24 items divided into 3 subscales: * Pain (5 items): During walking, using stairs, in bed, sitting or lying, and standing upright; * Stiffness (2 items): After first waking and later in the day Physical Function (17 items).The scores for each subscale are summed up, with a possible score range of 0-20 for Pain, 0-8 for Stiffness, and 0-68 for Physical Function.Higher scores on the WOMAC indicate worse pain, stiffness, and functional limitations
joint position sense	up to four weeks	using digital inclinometer for target angle 30 degree knee flexion

Trial Locations

Locations (1)

Hoda Mohamed Ahmed; 🇪🇬 Giza, Egypt