Skip to content

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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05812898
Enrollment
42
Registered
2023-04-14
Start date
2023-01-01
Completion date
2023-05-15
Last updated
2024-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Keywords

myofascial release, Knee osteoarthritis, Deep front line

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.

Interventions

OTHERexercises

strengthening of the gluteus maximus and medius, calf muscles stretching for calf and hamstring muscles

OTHERmyofascial release

myofascial release using instrument assisted soft tissue mobilization

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

exercise plus myofascial release of the adductor and tipialis posterior muscles.

Eligibility

Sex/Gender
ALL
Age
45 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
pain intensityup to four weeksThe 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
functionup to four weeksThe 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
rang of motionup to four weeksusing digital inclinometer
joint position senseup to four weeksusing digital inclinometer for target angle 30 degree knee flexion

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026