Effects of Feldenkrais Exercises in Knee Osteoarthritis Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40-60
SponsorRiphah International University

About this trial

The primary objective of the study is to determine the effects of Feldenkrais Exercises on Pain, Range of Motion, and Disability in Patients with Knee osteoarthritis. Knee osteoarthritis poses significant challenges in pain management, mobility improvement, and disability reduction among middle-aged to older adults. Feldenkrais Method offers benefits comparable to back school lessons or core stability exercises. This study, conducted as a Randomized Controlled Trial at RIPHAH Rehabilitation Clinic, aims to assess the efficacy of Feldenkrais exercises compared to conventional physical therapy in addressing pain, range of motion, and disability in knee osteoarthritis patients aged 40-60 years. A non-probability convenience sampling method will recruit 32 participants meeting specific criteria for osteoarthritis severity and functional ability. Participants will be randomly assigned to Group A (Feldenkrais exercises) or Group B (conventional therapy), with interventions delivered over four weeks. Group A will engage in Feldenkrais exercises targeting pelvic and lower limb mobility, while Group B will receive standard treatments including knee isometrics, mobilization, transcutaneous electric nerve stimulation, and heating pad applications. Pain severity will be measured using the Numeric Pain Rating Scale, Range of Motion assessed via goniometry, and disability evaluated using the Western Ontario McMaster Universities Osteoarthritis Index. Statistical analysis using SPSS will compare outcomes between groups at baseline, post-treatment, and follow-up assessments.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age between 40 to 60 years of patients.

Both female and male

Able to walk for 6 minutes (Timed up-and-go test)

Able to rise from floor

Disqualifiers

• Tuberculosis, carcinoma, heart disease, and osteoporosis

Any trauma or localized infection in the knee joint

Hyper flexibility

Open sores

Trial design

Design model

Parallel

Treatments tested in this trial

  • Feldenkrais exercises

    Other intervention

    Feldenkrais exercises focused on pain, improving mobility, and disability.

  • Standard physical therapy interventions

    Other intervention

    * Knee Isometrics: Isometric exercises targeting the quadriceps and hamstrings, performed for 10 minutes, twice a week. * Knee Mobilization * Transcutaneous Electric Nerve Stimulation (TENS). * Heating Pad Duration: 30-minute sessions, conducted twice a week for 4 weeks.

Treatment groups

32 Participants
are divided into 2 treatment groups
Group A: Group-A (Feldenkrais exercises)Experimental treatment 1 intervention
Group B: Group-B (Standard Physicaltherapy interventions)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Numeric Pain Rating Scale

The NPRS is a segmented numeric scale in which the respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain. The common format is a horizontal bar or line. NPRS is anchored by terms describing pain severity extremes.

Time frame
upto 4 weeks
2

Western Ontario and McMaster Universities Arthritis Index (WOMAC)

WOMAC is a disease-specific measure of health status (pain, stiffness, and function) in OA sufferers. It is widely used for evaluating hip and knee osteoarthritis. It is a self-administered questionnaire consisting of 24 items divided into 3 subscales

Time frame
upto 4 weeks
3

Universal Goniometer (UG)

A universal goniometer is a crucial tool in orthopedics used to precisely measure joint angles. It exists in two primary forms: the short-arm version is ideal for smaller joints such as the wrist, elbow, or ankle, while the long-arm version is more accurate for joints with longer levers like the knee and hip. It highlighting its role in quantifying joint mobility and aiding in treatment planning and assessment in medical practice.

Time frame
upto 4 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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