- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05723029
Bowen Technique and Post Isometric Relaxation in Knee Osteoarthritis Patients
April 18, 2023 updated by: Riphah International University
Comparative Effects of Bowen Technique and Post Isometric Relaxation on Pain, Range of Motion and Hamstring Flexibility in Knee Osteoarthritis Patients
The Hamstring muscles are present at the posterior surface of the thigh.
The muscles start in the gluteal region and run back of the thigh and insert into the popliteal fossa.
The function of hamstring muscles flexes the knee and extension of the thigh.
In degenerative joint disease, muscles tightness of the lower extremity leads to a decrease in joint flexibility.
In knee joint osteoarthritis, hamstring muscles are more prone to tightness.
The objective of this study is to compare the effects of the Bowen technique and Post Isometric Relaxation on pain, range of motion, and hamstring flexibility in knee osteoarthritis patients.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study will be a randomized clinical trial and will be conducted at Al- Mustafa Medical and Physiotherapy Center.
The study will be completed within the time duration of six months.
For data collection, a convenient sampling technique will be used.
The Population will be diagnosed with osteoarthritis patients.
A sample size of total 24 patients will be taken in this study.
The measurement tool will be Active knee extension test, Goniometer and Numeric pain rating scale.
The pre-test and post-test outcome measurement will be taken.
Patients will be divided into two groups.
Group A will receive the Bowen technique intervention and Group B will receive the Post Isometric Relaxation technique.
The interventions groups will receive three sessions per week for 4 weeks.
Study Type
Interventional
Enrollment (Actual)
20
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 Locations
-
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Punjab
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Lahore, Punjab, Pakistan, 54000
- Al-Mustafa Medical and Physiotherapy Center
-
-
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
45 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Symptomatic subjects with hamstring tightness
- Both male and female
- Age between 45 to 65
- O degree to 20-degree active knee extension loss
- Subject with inter-articular knee joint pathology
- Diagnosed osteoarthritis patients
- Grade 1 to 4 Osteoarthritis
Exclusion Criteria:
- Subject history of lower extremity injury
- Any Neurological symptoms or radiating pain
- Any lower limb deformity
- Any fracture or Surgery is done for knee
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: Bowen Technique
The subjects will receive Bowen Technique.
The treatment session will be 3 times per week for 4 weeks for 20 minutes.
The Bowen technique is a subtle and precise mobilization called Bowen moves.
The mobilization is applied by using the fingers and thumbs over muscles, tendon, nerves and fascia.
Only gentle non-invasive pressure is applied.
A Bowen moves challenges the muscles for several seconds by the application of a gentle lateral pressure applied by the therapist thumb, against its medial edge.
The muscle fibres and its fascia are disturbed from their neutral position and they are slightly stretched.
The therapist apply gentle pressure towards the muscles using the skin slack available, and then rolls the thumb across the muscles and gently compressing it, the muscle will bounce back to its original position.
The therapist has a sense of tissue tension, and this enables his/her to feel where stress has built up in the tissue.
|
A Bowen moves challenges the muscles for several seconds by the application of a gentle lateral pressure applied by the therapist thumb, against its medial edge.
The muscle fibres and its fascia are disturbed from their neutral position and they are slightly stretched.
The therapist apply gentle pressure towards the muscles using the skin slack available, and then rolls the thumb across the muscles and gently compressing it, the muscle will bounce back to its original position.
|
|
Experimental: Group B: Post Isometric Relaxation Technique
The subjects will receive Post Isometric Relaxation Technique.
Treatment session includes 3 times per week for 4 weeks for 20 minutes.
Evaluation will be done before and after the treatment at the end of the 4th week.
The outcome will be measured by the Active Knee Extension test, Numeric pain Rating Scale, and Goniometer.
Post Isometric Relaxation is performed in supine position on treatment table.
The therapist passively flexed the hip and knee at the 90 degrees and then passively extends the knee until the point of tissue resistance.
Patient placed their leg on therapist shoulder and contracts his hamstring muscles by pushing down on the therapist shoulder for 10 seconds.
After the contraction, patient is asked to relax, then therapist passively stretch to gain new range of muscles.
The intervention is performed three times in a single session with 30 seconds rest intervals.
|
Post Isometric Relaxation is performed in supine position on treatment table.
The therapist passively flexed the hip and knee at the 90 degrees and then passively extends the knee until the point of tissue resistance.
Patient placed their leg on therapist shoulder and contracts his hamstring muscles by pushing down on the therapist shoulder for 10 seconds.
After the contraction, patient is asked to relax, then therapist passively stretch to gain new range of muscles.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Active knee extension test
Time Frame: Baseline measurement (Pre-Treatment) in start on 1st day and post treatment follow-up for change will be taken on 4th week
|
In this test, the subject is on the left-side lying on the examination table for bony landmark identification.
The lateral femoral condyle, head of a fibula, and lateral malleolus of the right leg are marked to ensure that the same reference point is used for repeated measurement.
When the landmarks are identified, the subject is instructed to lie in the supine position.
The subject flexes the right hip at 90 degrees and grasps behind the right knee to stabilize the hip at 90 degrees.
A goniometer is used to position the right knee at 90 degrees.
A stationary arm long lateral femur and movable arm aligned with lateral fibula keeping lateral femoral condyle as an axis.
The Patient actively extends the right knee as much as possible without moving the thigh from a vertical position.
The active Range of motion of the knee is measured by a goniometer.
(7) The active knee extension test have excellent intra-rater reliability(r = .7).
|
Baseline measurement (Pre-Treatment) in start on 1st day and post treatment follow-up for change will be taken on 4th week
|
|
Change in Numeric pain rating scale
Time Frame: Baseline measurement (Pre-Treatment) in start at at 1st week and post treatment follow-up for change will be taken on4th week
|
The Numeric pain rating scale is a self-reported measurement tool consisting of a numerical point scale.
The scale is set up on a horizontal or vertical line, which ranges most commonly from 0 to 10, where 0 is no pain and 10 is the worst pain.
The patient is asked to rate his or her pain intensity.
There are three categories of pain least pain, average pain and, worst pain.
The test-retest reliability for the Numeric pain rating scale varies from 0.67 to 0.96.
|
Baseline measurement (Pre-Treatment) in start at at 1st week and post treatment follow-up for change will be taken on4th week
|
|
Change in Goniometer test
Time Frame: Baseline measurement (Pre-Treatment) in start on 1st day and post treatment follow-up for change will be taken on 4th week
|
In this test, each subject is in the supine position, while a small pillow is placed beneath his head and neck.
Then the legs and thighs of the other lower extremity are fixed to the bed with a strap.
The knee flexion axis is being marked by a pen and from this point; a line is being drawn to the greater trochanter of the femur and one other line to the external malleolus of the ankle.
These lines are used to measure the knee joint angles.
The goniometer axis is placed on the knee axis and its arm is the place along with the line drawn on the thigh and the other arm is placed along with the line drawn on the leg.
The Hip joint is 90 degrees and the vertical position of the thigh is being maintained.
The subject is asked to do the active Knee extension slowly while the ankle is in the neutral position.
|
Baseline measurement (Pre-Treatment) in start on 1st day and post treatment follow-up for change will be taken on 4th week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
- Marr M, Baker J, Lambon N, Perry J. The effects of the Bowen technique on hamstring flexibility over time: a randomised controlled trial. J Bodyw Mov Ther. 2011 Jul;15(3):281-90. doi: 10.1016/j.jbmt.2010.07.008. Epub 2010 Sep 15.
- Shamsi M, Mirzaei M, Khabiri SS. Universal goniometer and electro-goniometer intra-examiner reliability in measuring the knee range of motion during active knee extension test in patients with chronic low back pain with short hamstring muscle. BMC Sports Sci Med Rehabil. 2019 Mar 22;11:4. doi: 10.1186/s13102-019-0116-x. eCollection 2019.
- Neto T, Jacobsohn L, Carita AI, Oliveira R. Reliability of the Active-Knee-Extension and Straight-Leg-Raise Tests in Subjects With Flexibility Deficits. J Sport Rehabil. 2015 Dec 3;24(4):2014-0220. doi: 10.1123/jsr.2014-0220. Print 2015 Nov 1.
- Kahl C, Cleland JA. Visual analogue scale, numeric pain rating scale and the McGill pain Questionnaire: an overview of psychometric properties. Physical therapy reviews. 2005;10(2):123-8.
- Khuman PR, Surbala L, Patel P, Chavda D. Immediate effects of single session post isometric relaxation muscle energy technique versus mulligan's bent leg raise technique on pain and hamstring flexibility in knee osteoarthritis participants: A randomised controlled study. Physiotherapy. 2014;3(9):324-35.
- Masekar MB, Rayjade DA, Yadav DT, Chotai DK. Effectiveness of Muscle Energy Technique and Proprioceptive Neuromuscular Facilitation in Knee Osteoarthritis.(2021). Int J Life SciPharmaRes.11(1):L16- 22.
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 18, 2023
Primary Completion (Actual)
March 31, 2023
Study Completion (Actual)
March 31, 2023
Study Registration Dates
First Submitted
January 24, 2023
First Submitted That Met QC Criteria
February 9, 2023
First Posted (Actual)
February 10, 2023
Study Record Updates
Last Update Posted (Actual)
April 19, 2023
Last Update Submitted That Met QC Criteria
April 18, 2023
Last Verified
April 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/22/0156
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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