- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02707679
Comparison of Effects of Mobilization With Movement and Kinesiotaping in Patellofemoral Pain Syndrome
March 13, 2016 updated by: SERDAR DEMIRCI, Hacettepe University
Comparison of Short-Term Effects of Mobilization With Movement and Kinesiotaping on Pain, Function and Balance in Patellofemoral Pain Syndrome: A Randomized Control
Patellofemoral Pain Syndrome (PFPS), also known as the anterior knee pain, is one of the most common musculoskeletal disorders.
Most of the patients suffer from knee pain for long time.
The aim of this study was to investigate the short-term effects of Mobilization with movement and Kinesiotaping on pain, function and balance in patient with PFPS.
Study Overview
Status
Completed
Conditions
Detailed Description
Patellofemoral Pain Syndrome is one of the most common musculoskeletal problem in the world.
It's incidence is also becoming higher and most people who have knee pain suffer from it for long time.
In the treatment of PFPS, conservative treatment methods are preferred prior to surgical ones.
When the literature was reviewed, no study in which Mobilization with movement (MWM) method was used and in which the effects of it was shown and compared with (Kinesiotaping) KT has been found so far with respect to the treatment of PFPS.
Thirty-five female patients diagnosed with unilateral PFPS were randomly assigned into 2 groups.
The patients in the first group (n=18) received two techniques of Mobilization with movement intervention while Kinesiotaping was applied to the other group (n=17).
Both groups were treated with exercise.
All patients received 4 sessions of treatment twice a week for a period of 2 weeks and followed up in accordance with a 6-week-home exercise program.
Primary outcomes: pain severity, knee range of motion, hamstring flexibility, and physical performance (10-step stair climbing test, timed up and go test), Kujala Patellofemoral Pain Scoring and Y-Balance test were assessed.
Study Type
Interventional
Enrollment (Actual)
35
Phase
- Not Applicable
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
20 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- having knee pain at least 3 months and more than 3 points according to visual analog scale
Exclusion Criteria:
- no complying to the rehabilitation
- if patient wants to finished and want to complete study, they were excluded
- having meniscus, bursa, ligament, patellar tendon lesions, patellofemoral dislocation and/or recurrent subluxation, undergone lower extremity surgery
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 |
|---|---|
|
Other: Effects of Mulligan's Mobilization
The patients in this arm (n=18) received two techniques pertaining to Mulligan's Mobilization with movement approach (Mulligan's Straight Leg-Raise with Traction and Tibial Gliding) along with an exercise therapy.
Patients received 4 sessions of treatment twice a week for a period of 2 weeks and followed up in accordance with a 6-week-home exercise program.
Primary outcomes: pain severity, knee range of motion, hamstring flexibility, and physical performance (10-step stair climbing test, timed up and go test), Kujala Patellofemoral Pain Scoring and Y-Balance test were assessed before the treatment, 45 minutes after the initial treatment, at the end of the 4-session-treatment during 2-week period and 6 weeks later.
|
Mulligan's Straight leg raise technique was performed on patients with patellofemoral pain syndrome.
The extremity on which the practice would be performed in supine position was grasped from the ankle level and was, then, subjected to traction longitudinally.
Afterwards, the knee was lifted up passively while in extension and was kept for waiting for a few seconds at the point where tension was felt and was, then, returned to its initial position.
The practice was repeated 10 times, and 3 sets of practice at 1-minute-intervals were performed.
Mulligan's Mobilization with Movement technique was performed on patients with patellofemoral pain syndrome.
Each patient was tested in every direction in the course of the active knee flexion-extension movement so as to find out the best pain-free tibial gliding direction (medial-lateral part of the tibia, anterior-posterior, internal-external rotation).
At the time of the active movement of the knee, the tibial gliding direction where pain was felt at the least was selected as the treatment direction of mobilization technique along with movement.
The practice was performed by doing 10 repetitions for 3 sets and by providing 1-minute-resting time between the sets.
All the patients were provided with several exercises within the scope of the home exercise program, such as hamstring muscle stretching, quadriceps isometric exercises, 4-way-strengthening with exercise elastic bands for the muscles of the hip, knee locking on foot and mini-squatting exercises.
They were asked to do these exercises in 3 sets a day along with 10 repetitions for a period of 6 weeks.
|
|
Other: Effects of Kinesiotaping
Patients in this arm were applied kinesiotaping on quadriceps and hamstring muscle along with an exercise therapy.
Patients received 4 sessions of treatment twice a week for a period of 2 weeks and followed up in accordance with a 6-week-home exercise program.
The same assessment parameters was conducted on this arm too.
|
All the patients were provided with several exercises within the scope of the home exercise program, such as hamstring muscle stretching, quadriceps isometric exercises, 4-way-strengthening with exercise elastic bands for the muscles of the hip, knee locking on foot and mini-squatting exercises.
They were asked to do these exercises in 3 sets a day along with 10 repetitions for a period of 6 weeks.
Kinesiotaping was applied on patient with patellofemoral pain syndrome.
To maintain proprioceptive stimulation in the quadriceps (from origo towards insertio) and to alleviate the tension of hamstring muscle, a 'Y''-shaped kinesiotape was applied by using the muscle technique.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee pain measured with Visual Analog Scale
Time Frame: 6 weeks
|
Patient's knee pain was measured with Visual Analog Scale
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee joint range of motion was measured Universal goniometer.
Time Frame: 6 weeks
|
Universal goniometer was used for evaluating the knee joint range of motion.
|
6 weeks
|
|
Balance measured with Y- Balance Test
Time Frame: 6 weeks
|
The dynamic balance measurements of the patients were evaluated through Y- Balance Test
|
6 weeks
|
|
Function was measured with 10-step-ascent & descent stair-climbing test.
Time Frame: 6 weeks
|
To evaluate the functional performances of the patients, 10-step-ascent & descent stair-climbing test was used.
|
6 weeks
|
|
Function was measured Kujala patellofemoral scoring system
Time Frame: 6 weeks
|
Patient's function was measured with Kujala patellofemoral scoring system
|
6 weeks
|
|
Function was measured with timed up&go test
Time Frame: 6 weeks
|
To evaluate the functional performances of the patients, timed up&go test was used.
|
6 weeks
|
|
Hamstring muscle flexibility was measured Universal goniometer.
Time Frame: 6 weeks
|
Universal goniometer was used for evaluating the hamstring muscle flexibility.
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Volga Bayrakcı Tunay, Prof., supervisor of the study
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
- Djordjevic OC, Vukicevic D, Katunac L, Jovic S. Mobilization with movement and kinesiotaping compared with a supervised exercise program for painful shoulder: results of a clinical trial. J Manipulative Physiol Ther. 2012 Jul;35(6):454-63. doi: 10.1016/j.jmpt.2012.07.006. Epub 2012 Aug 24. Erratum In: J Manipulative Physiol Ther. 2012 Oct;35(8):659.
- Kuru T, Yaliman A, Dereli EE. Comparison of efficiency of Kinesio(R) taping and electrical stimulation in patients with patellofemoral pain syndrome. Acta Orthop Traumatol Turc. 2012;46(5):385-92. doi: 10.3944/aott.2012.2682.
- Collado H, Fredericson M. Patellofemoral pain syndrome. Clin Sports Med. 2010 Jul;29(3):379-98. doi: 10.1016/j.csm.2010.03.012.
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
May 1, 2013
Primary Completion (Actual)
August 1, 2015
Study Completion (Actual)
August 1, 2015
Study Registration Dates
First Submitted
March 2, 2016
First Submitted That Met QC Criteria
March 8, 2016
First Posted (Estimate)
March 14, 2016
Study Record Updates
Last Update Posted (Estimate)
March 15, 2016
Last Update Submitted That Met QC Criteria
March 13, 2016
Last Verified
March 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- LUT 12/175
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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