- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02007668
Is Kinesio Taping More Effective Than Medical Adhesive Tape in Patients With Chronic Non-specific Low Back Pain?
December 5, 2013 updated by: Mauricio Antonio da Luz Junior, Paulista University
Is Kinesio Taping More Effective Than Medical Adhesive Tape in Patients With Chronic Non-specific Low Back Pain? A Randomized Controlled Trial
Sixty patients will be randomized into three groups to receive the Kinesio taping, placebo Kinesio taping (medical adhesive tape) and control group.
The group Kinesio taping receive the correct application of the method described.
The placebo group will receive a medical adhesive tape.
The control group will not receive any form of intervention.
Study Overview
Detailed Description
The group Kinesio taping receive the correct application of the method described with tension paper off (10-15%).
The placebo group will receive a medical adhesive tape.
The control group will not receive any form of intervention.
Study Type
Interventional
Enrollment (Actual)
60
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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São Paulo
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Jundiaí, São Paulo, Brazil, 13214-525
- Universidade Paulista - UNIP
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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
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients with non-specific low back pain longer than 3 months
- Seeking care for low back pain
Exclusion Criteria:
- Contra indications to any bandage
- Serious sinal pathologies (e.g. tumors, fractures and inflammatory diseases)
- Nerve roto compromise
- Pregnancy
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: Kinesio Taping
Patients will receive an application of Kinesio taping in their lumbar spine.
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Kinesio taping intervention is based upon the use of specific elastic tapes (known as Kinesio Tex Gold) that are applied with a certain amount of tension fixed to the skin of patients with the target muscles in a stretched position.
The tapes will be placed over the lumbar spine.
Other Names:
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Placebo Comparator: Kinesio Taping Placebo
Patients will receive an application of medical adhesive tape in their lumbar spine.
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No Intervention: Control
This participants will not receive intervention
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain Intensity
Time Frame: 2 days
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Pain Intensity will be measured in 2 and 7 days after randomization by an 11-point (0-10) Numerical Rating Scale (Pain NRS)
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2 days
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Disability
Time Frame: 2 days
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Disability associated with low back pain will be measured in 2 and 7 days after randomization by the 24-item Roland Morris Disability Questionnaire
|
2 days
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mauricio Antonio da Luz Junior, MSc, Paulista 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
August 1, 2013
Primary Completion (Actual)
August 1, 2013
Study Completion (Actual)
November 1, 2013
Study Registration Dates
First Submitted
November 30, 2013
First Submitted That Met QC Criteria
December 5, 2013
First Posted (Estimate)
December 11, 2013
Study Record Updates
Last Update Posted (Estimate)
December 11, 2013
Last Update Submitted That Met QC Criteria
December 5, 2013
Last Verified
December 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CAAE:16832013.9.0000.5512
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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