- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02029391
Kinesio Taping in Subjects With Myofascial Pain Syndrome: a Randomized Controlled Trial
January 7, 2014 updated by: National Taiwan University Hospital
Kinesio Taping on Short Term Changes in Subjects With Myofascial Pain Syndrome: a Randomized Controlled Trial
Musculoskeletal dysfunction is considered as a major public health problem affecting about one third of the adult population.
Myofascial pain syndrome (MPS) characterized by myofacial trigger points as well as fascia tenderness are thought to be the main cause of musculoskeletal dysfunction.
The aim of the treatment for musculoskeletal dysfunction is to reduce pain and restore normal function.
Clinically, some evidence supports the application of kinesio tape in these patients.
The underlying mechanism, however, is not clear.
The investigators goal was to validate proposed mechanism of kinesio tape in these patients.
The primary outcome are muscle stiffness, pain intensity and sensitivity.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
31
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
-
-
-
Taipei, Taiwan, 100
- Institute of Physical Therapy, National Taiwan University
-
-
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 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- age between 20 and 60 years
- shoulder or neck pain corresponding with the area covered by the upper trapezius muscle
- Trigger point (taut band) in the upper trapezius muscle
Exclusion Criteria:
- diagnosis of fibromyalgia syndrome
- having undergone myofascial therapy within the past month before the study
- history of cervical spine or shoulder surgery
- previous history of a whiplash injury;
- diagnosis of cervical radiculopathy or myelopathy;
- taking medicine that might change the pain intensity or pain threshold, such as analgesics, sedatives, substance abuse (including alcohol, narcotics);
- a cognitive impairment that would prevent them from being able to understand and/or participate fully in the intervention or the measures.
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Myofascial pain syndrome patients
Manual pressure release only
|
Therapist applied non-painful pressure with slowly increase over the myofascial trigger point until he felts a tissue resistance barrier.
|
Experimental: Myofascial pain syndrome
One session of manual pressure release and kinesio tape
|
Therapist applied non-painful pressure with slowly increase over the myofascial trigger point until he felts a tissue resistance barrier.
Kinesio tape was adhered from insertion to origin of the upper trapezius muscle
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Muscle stiffness
Time Frame: baseline, immediate after intervention and at week 1
|
baseline, immediate after intervention and at week 1
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Visual analog scale (VAS)
Time Frame: baseline, immediate after intervention and at week 1
|
baseline, immediate after intervention and at week 1
|
Pressure pain threshold
Time Frame: baseline, immediate after intervention and at week 1
|
baseline, immediate after intervention and at week 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Jiu-Jeng Lin, PhD, Institute of Physical Therapy, National Taiwan University
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
October 1, 2013
Primary Completion (Actual)
November 1, 2013
Study Completion (Actual)
December 1, 2013
Study Registration Dates
First Submitted
January 6, 2014
First Submitted That Met QC Criteria
January 6, 2014
First Posted (Estimate)
January 7, 2014
Study Record Updates
Last Update Posted (Estimate)
January 9, 2014
Last Update Submitted That Met QC Criteria
January 7, 2014
Last Verified
January 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201304048RINB
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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-
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