Effects of Myofascial Release and Neuromuscular Training for Pes Anserine Syndrome Associated With Knee Osteoarthritis

Not Applicable

Completed

• Conditions: Pes Anserine Bursitis; Knee Osteoarthritis
• Interventions: Other: Neuromuscular exercises; Other: Myofascial release; Other: Cold pack

• Registration Number: NCT05529914
• Lead Sponsor: Dow University of Health Sciences

Brief Summary

A randomized control trial will be conducted at the outpatient department of Dow Institute of Physical Medicine and Rehabilitation. A sample size of 80 is calculated using PASS version 11 software. The subjects will be first screened and those who fulfill the inclusion criteria, will be asked to fill the consent form. After selection, the participants will be randomly allocated by the help of computer generated randomization sheet, into two groups i.e. experimental and the control group. The group A will be provided with the myofascial release along with the neuromuscular training whereas the group B will only receive the neuromuscular training. Cold pack will be applied to both the groups. The neuromuscular training consists of warm-up phase, lunges, sideways exercises, wall squats, weight transfer exercises, step up and down and the cool down phase. Total 12 sessions of 35 minutes each will be given to all the participants for about 4 weeks on alternate days. Outcome measures will be analyzed by visual analogue scale (VAS) for pain assessment, goniometry for range of motion and the Knee injury and Osteoarthritis Outcome Score (KOOS) to evaluate the functional assessment of the patients at the baseline and the post intervention.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2022-09-03
• Study First Submitted QC: 2022-09-03
• Study First Posted: 2022-09-07
• Study Start: 2022-09-27
• Primary Completion: 2023-03-30
• Study Completion: 2023-04-30
• Status Verified: 2024-01
• Last Update Submitted: 2024-01-07
• Last Update Posted: 2024-01-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

• Male and Females both with the age between 40-60 years.
• Patients with unilateral or bilateral knee osteoarthritis with pes anserine syndrome.
• Patients with knee pain more than 3.4 cm on visual analogue scale as minimum cut of value.
• Kellgren and Lawrence grade II and III on radiological findings.
• Duration of knee osteoarthritis more than 3 months (chronic).

Exclusion Criteria

• Patients with any neurological disorder.
• Knee deformities such as contractures, genu valgum and genu varum.
• Septic knee arthritis.
• History of ligamentous injury or meniscal tear.
• Cancer or any other malignancy or bone tumor.
• Any history of previous lower limb arthroplasty or other knee surgery.
• Comorbid like diabetes mellitus.
• Inflammatory rheumatic disease (R.A).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Neuromuscular exercises + Cold pack	Neuromuscular exercises	-
Myofascial release + Neuromuscular exercises + Cold pack	Cold pack	-
Neuromuscular exercises + Cold pack	Cold pack	-
Myofascial release + Neuromuscular exercises + Cold pack	Neuromuscular exercises	-
Myofascial release + Neuromuscular exercises + Cold pack	Myofascial release	-

Primary Outcome Measures

Name	Time	Method
Change in pain intensity on visual analogue scale after four weeks	Baseline and 4 weeks	The Visual Analogue Scale is a unidimensional measure of pain intensity, used to record patients' pain progression, or compare pain severity between pains with similar conditions.. It is 0 to 10 cm scale. Patients rate their pain on that scale. Higher the score in centimeter, severe will be the pain experienced.
Change in range of motion assessed with universal goniometer after four weeks	Baseline and 4 weeks	The Goniometer is an instrument for the precise measurement of range of movement angles in degree , especially one used to measure the angles before and after range of motion.. Increase in the degree of angle suggests increase in range of movement.

Secondary Outcome Measures

Name	Time	Method
Change in functional disability assessed with Knee injury and osteoarthritis outcome score after four weeks.	Baseline and 4 weeks	The Knee Injury and Osteoarthritis Outcome Score (KOOS) is a knee-specific instrument, developed to assess the patients' opinion about their knee and associated problems regarding functional disability. In consists of total 100 scores. Increase in scores suggests decreased functional disability and decrease in scores suggests increased functional disability.

Trial Locations

Locations (2)

Dow Institute of Physical Medicine and Rehabilitation; 🇵🇰 Karachi, Sindh, Pakistan

Sindh Institute of Physical Medicine and Rehabilitation; 🇵🇰 Karachi, Sindh, Pakistan