- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06954363
Effectiveness of Muscle Energy Techniques and Mulligan Mobilization Along With Conventional Physical Therapy in Knee Joint Osteoarthritis Patients
Effectiveness of Muscle Energy Techniques and Mulligan Mobilization Along With Conventional Physical Therapy in Knee Joint Osteoarthritis Patients: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Osteoarthritis (OA) is a progressive degenerative joint disease characterized by the destruction of articular cartilage and the formation of bone spurs, leading to pain, joint stiffness, and decreased functional mobility. While its exact cause remains unknown, factors such as age, sex, obesity, sedentary lifestyle, genetics, bone density, smoking, and joint location contribute significantly to its development. As patients experience pain and reduced joint mobility, they often limit movement, particularly of the knee, resulting in muscular tightness-most notably in the hamstring, a two-joint muscle.
Globally, OA is a major public health concern, with knee OA affecting approximately 250 million people in 2010, including 18% of women and 9.6% of men over 60. It has substantial economic impacts, such as costing the United States 1-2.5% of its GDP and Spain €4.7 billion in 2007. Regional data from South Asia show higher prevalence in rural populations, emphasizing the disease's widespread burden.
Physical therapy has been shown to be highly effective in managing knee OA symptoms. Several randomized controlled trials support the use of techniques like Muscle Energy Technique (MET) and Mulligan Mobilization. MET has demonstrated superior efficacy compared to static stretching and whole-body vibration in improving hamstring flexibility and reducing stiffness. Similarly, Mulligan Mobilization, particularly when combined with supervised exercises, has shown better outcomes than Maitland mobilization in improving flexibility and function in OA patients.
However, current literature presents conflicting evidence regarding the individual efficacy of MET and Mulligan Mobilization. This study seeks to address these inconsistencies by investigating the effectiveness of integrating both MET and Mulligan Mobilization with conventional physical therapy in treating knee OA. The goal is to provide evidence-based insights that can guide clinicians in optimizing therapeutic strategies for better functional outcomes and enhanced quality of life for patients with knee osteoarthritis.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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KPK
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Peshawar, KPK, Pakistan, 25000
- Hayatabad Medical Complex Peshawar
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Peshawar, KPK, Pakistan
- Alkhidmat Hospital Peshawar
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Peshawar, KPK, Pakistan
- Bibi Zahida Memorial Hospital, NCS University System
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Diagnosed cases of osteoarthritis (Grade 1 to 3)
- X-ray showing Grades I to III on Kellgren Lawrence scale of Osteoarthritis.
- Residents of Peshawar verified via NADRA CNIC
- Both genders will be included with unilateral or bilateral knee involvement.
- Age group 40 and above.
- Duration of Knee pain for more than 3 months.
Exclusion Criteria:
- History of any previously known neurological conditions i.e. stroke, peripheral neuropathy
- Fractures in treatment limb.
- Suspicious of malignancy around the knee joint.
- Recent under gone surgery
- Recent Intra-articular injection.
- Significant comorbid diseases and disabilities are excluded from the study
Study Plan
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 |
|---|---|
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Experimental: Intervention Group
Participants in this group will receive Mulligan Mobilization combined with Conventional Physical Therapy.
Mulligan Mobilization includes medial and lateral tibial glides using a Mulligan belt.
Each session will consist of 3 sets of 10 repetitions, administered 5 days a week for 3 weeks.
In addition, patients will undergo standard conventional physical therapy exercises such as quadriceps strengthening, straight leg raising, and stretching exercises.
Each treatment session will last 30 minutes.
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Mulligan Mobilization involves manual tibial glides (medial and lateral) using a mobilization belt.
The patient lies supine with the knee flexed between 30°-45°.
The therapist applies a sustained glide while the patient actively moves the knee into flexion and extension.
The treatment is delivered in 3 sets of 10 repetitions per session, 5 days per week for 3 weeks, along with a conventional physical therapy protocol.
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Active Comparator: Control Group
Participants in this group will receive Muscle Energy Technique (MET) targeting the hamstring muscles, in combination with Conventional Physical Therapy.
The MET will follow a post-isometric relaxation approach, using both direct and indirect methods depending on patient condition.
Each isometric contraction will be held for 10 seconds, followed by a 20-second stretch, repeated for 3 sets.
Therapy will be conducted 5 days a week over a 3-week period.
Each session will last 30 minutes.
The same conventional physical therapy regimen as the intervention group will be applied.
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Muscle Energy Technique involves the application of post-isometric relaxation targeting hamstring muscles.
The therapist applies a 10-second isometric contraction at the resistance barrier, followed by a 20-second passive stretch, progressing into a new range of motion.
This technique is applied 3 times per session, 5 days per week for 3 weeks, in combination with a conventional physical therapy protocol.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hamstring Flexibility Measured by Goniometer
Time Frame: Baseline (Day 1) and Post-treatment (End of Week 3)
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Hamstring range of motion (ROM) will be assessed using a goniometer before and after the intervention. The change in ROM will be used to evaluate effectiveness. Outcome improvement categories: Mild Increase: 5-10 degrees Moderate Increase: 10-15 degrees Marked Increase: >15 degrees |
Baseline (Day 1) and Post-treatment (End of Week 3)
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Change in Pain Score Using Knee Osteoarthritis Outcome Score-12 questionnaire Questionnaire
Time Frame: Baseline (Day 1) and Post-treatment (End of Week 3)
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The function in daily activities subscale of Knee Osteoarthritis Outcome Score-12 questionnaire will assess participants' ability to perform routine activities before and after the intervention.
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Baseline (Day 1) and Post-treatment (End of Week 3)
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Change in Knee-Related Quality of Life Using Knee Osteoarthritis Outcome Score-12 questionnaire
Time Frame: Baseline (Day 1) and Post-treatment (End of Week 3)
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The quality of life (QOL) subscale of KOOS-12 will evaluate the impact of osteoarthritis on participants' knee-related wellbeing pre- and post-treatment.
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Baseline (Day 1) and Post-treatment (End of Week 3)
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Change in Activity of Daily Living Function Using KOOS-12
Time Frame: Baseline (Day 1) and Post-treatment (End of Week 3)
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The function in daily activities subscale of KOOS-12 will assess participants' ability to perform routine activities before and after the intervention.
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Baseline (Day 1) and Post-treatment (End of Week 3)
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Collaborators and Investigators
Investigators
- Principal Investigator: Babar Israr, MSPT, Institute of Physical Medicine and Rehabilitation, Khyber Medical University Peshawar
- Study Director: Shakir Ullah, PhD, Institute of Physical Medicine and Rehabilitation, Khyber Medical University Peshawar
- Principal Investigator: Samra Farid, MSPT, Alkhidmat Hospital Peshawar
Publications and helpful links
General Publications
- Sanchez-Romero EA, Pecos-Martin D, Calvo-Lobo C, Ochoa-Saez V, Burgos-Caballero V, Fernandez-Carnero J. Effects of dry needling in an exercise program for older adults with knee osteoarthritis: A pilot clinical trial. Medicine (Baltimore). 2018 Jun;97(26):e11255. doi: 10.1097/MD.0000000000011255.
- Farazdaghi M, Kordi Yoosefinejad A, Abdollahian N, Rahimi M, Motealleh A. Dry needling trigger points around knee and hip joints improves function in patients with mild to moderate knee osteoarthritis. J Bodyw Mov Ther. 2021 Jul;27:597-604. doi: 10.1016/j.jbmt.2021.04.011. Epub 2021 Apr 30.
- Ceballos-Laita L, Jimenez-Del-Barrio S, Marin-Zurdo J, Moreno-Calvo A, Marin-Bone J, Albarova-Corral MI, Estebanez-de-Miguel E. Effects of dry needling on pain, pressure pain threshold and psychological distress in patients with mild to moderate hip osteoarthritis: Secondary analysis of a randomized controlled trial. Complement Ther Med. 2020 Jun;51:102443. doi: 10.1016/j.ctim.2020.102443. Epub 2020 May 18.
- Ashraf F, Anwar K, Arshad H. Effects of muscle energy technique along conventional physical therapy after mesenchymal stem cell transplantation in knee osteoarthritis patients. Pak J Med Sci. 2024 Dec;40(11):2558-2564. doi: 10.12669/pjms.40.11.9605.
- Goksen A, Can F, Yilmaz S, Korkusuz F. Comparison of different neuromuscular facilitation techniques and conventional physiotherapy in knee osteoarthritis. Turk J Med Sci. 2021 Dec 13;51(6):3089-3097. doi: 10.3906/sag-2101-298.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KMU/DIR/CTU/2024/015
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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