- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06875817
Effects of Feldenkrais Exercises in Knee Osteoarthritis Patients
March 10, 2025 updated by: Riphah International University
Effects of Feldenkrais Exercises on Pain, Range of Motion, and Disability in Patients With Knee Osteoarthritis
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.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Osteoarthritis (OA) is one of the most prevalent rheumatic diseases in the elderly, being a frequent cause of incapacity among this population.
It is more common in the knee and is characterized by pain, stiffness, and function loss.
OA is a major public health problem.
The prevalence of knee OA is 34-45% in the Indian population with clinical symptoms of pain, reduced muscle strength, and knee function.
That is the most common form of degenerative joint disease affecting 15 to 40% of people aged 40 and above.
One hundred fifty-one million people worldwide experienced OA, and it was ranked sixth as a leading cause of moderate and severe disability.
The knee is the joint most frequently affected by osteoarthritis.
The Feldenkrais Method has the potential to help older people with OA.
Developed by Dr. Moshe Feldenkrais, the method is a gentle form of exercise which has been shown to be acceptable for older people who have limited movement.
The Feldenkrais Method is taught in two parallel forms, Awareness Through Movement (conducted as a group exercise) and Functional Integration (one-on one approach).
This study explores the effectiveness of Awareness Through Movement lessons in helping older people with OA.
The method aims for improved functioning, where the entire body cooperates efficiently with minimal effort.
This study aims to explore the potential benefits of Feldenkrais exercises as an alternative, non-invasive treatment for knee osteoarthritis.
Medical conventional treatments for knee OA, such as pharmacotherapy and surgical interventions, often come with limitations including potential side effects, high costs, and sometimes limited long-term effectiveness.
These constraints necessitate the exploration of alternative, non-invasive treatment options that can be both effective and accessible.
Feldenkrais exercises focus on improving movement patterns and body awareness, which may help reduce pain, enhance range of motion, and decrease disability.
Study Type
Interventional
Enrollment (Estimated)
32
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: imran amjad, PhD*
- Phone Number: 03324390125
- Email: imran.amjad@riphah.edu.pk
Study Contact Backup
- Name: Imran Amjad, PHD*
- Phone Number: 051-5481826
- Email: imran.amjad@riphah.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan
- Recruiting
- RIPHAH Rehabilitation Clinic, Punjab, Pakistan
-
Contact:
- Ghulam Fatima, PhD
- Phone Number: 03034073057
- Email: ghulam.fatima@riphah.edu.pk
-
Principal Investigator:
- saliha Farooq, MS*
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- 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
- Grade 2 and 3 of osteoarthritis diagnosed with radiograph (Kellgren and Lawrence classification system)
- Pain reported on VAS score ˃6/10 in knee region for more than 3 months
Exclusion Criteria:
• Tuberculosis, carcinoma, heart disease, and osteoporosis
- Any trauma or localized infection in the knee joint
- Hyper flexibility
- Open sores
- Ongoing radiotherapy, chemotherapy, steroid therapy, or anticoagulants
- Psychiatric diseases such as phobia/obsession and depression
- Allergy to hot pack
- Patients with a history of surgery in the knee region within a year.
- Severe cognitive impairments
- Contraindications to physical activity
- Concurrent participation in other physical therapy programs
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group-A (Feldenkrais exercises)
This group of participants will engage in Feldenkrais exercises focused on pain, improved mobility, and disability.
Each session will last 30 minutes, conducted twice a week for 4 weeks.
The exercises include Pelvic Clock Exercise, Knee Rolling, Ankle Circles, Knee Flexion and Extension and Leg Slides.
|
Feldenkrais exercises focused on pain, improving mobility, and disability.
|
|
Active Comparator: Group-B (Standard Physicaltherapy interventions)
Participants will receive standard physical therapy interventions for knee osteoarthritis. Protocol:
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale
Time Frame: upto 4 weeks
|
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.
|
upto 4 weeks
|
|
Western Ontario and McMaster Universities Arthritis Index (WOMAC)
Time Frame: upto 4 weeks
|
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
|
upto 4 weeks
|
|
Universal Goniometer (UG)
Time Frame: upto 4 weeks
|
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.
|
upto 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ghulam Fatima, PHD*, Riphah International University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Zhang Y, Jordan JM. Epidemiology of osteoarthritis. Clin Geriatr Med. 2010 Aug;26(3):355-69. doi: 10.1016/j.cger.2010.03.001. Erratum In: Clin Geriatr Med. 2013 May;29(2):ix.
- Lespasio MJ, Piuzzi NS, Husni ME, Muschler GF, Guarino A, Mont MA. Knee Osteoarthritis: A Primer. Perm J. 2017;21:16-183. doi: 10.7812/TPP/16-183.
- Vincent KR, Vincent HK. Resistance exercise for knee osteoarthritis. PM R. 2012 May;4(5 Suppl):S45-52. doi: 10.1016/j.pmrj.2012.01.019.
- Brooks PM. The burden of musculoskeletal disease--a global perspective. Clin Rheumatol. 2006 Nov;25(6):778-81. doi: 10.1007/s10067-006-0240-3. Epub 2006 Apr 12.
- Salaffi F, Carotti M, Stancati A, Grassi W. Health-related quality of life in older adults with symptomatic hip and knee osteoarthritis: a comparison with matched healthy controls. Aging Clin Exp Res. 2005 Aug;17(4):255-63. doi: 10.1007/BF03324607.
- Webb R, Cofre Lizama LE, Galea MP. Moving with ease: feldenkrais method classes for people with osteoarthritis. Evid Based Complement Alternat Med. 2013;2013:479142. doi: 10.1155/2013/479142. Epub 2013 Sep 3.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 2, 2025
Primary Completion (Estimated)
September 2, 2025
Study Completion (Estimated)
September 15, 2025
Study Registration Dates
First Submitted
March 10, 2025
First Submitted That Met QC Criteria
March 10, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 10, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/24/0150
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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