Chronic Low Back Pain Clinical Trial
Official title:
Is Kinesio Taping Able to Influence the Electrical Activity of Muscles in Patients With Low Back Pain? A Controlled Randomized Trial
Objectives: To test if the Kinesio Tex Gold ® is able to change the electromyographic signal
of iliocostalis and longissimus muscles in patients with chronic nonspecific low back pain.
Study design: Three-arm, randomized controlled trial with a blinded assessor.
Location of study: Physical therapy Clinic of the Universidade Cidade de São Paulo (UNICID)
Patients: Sixty-three patients with chronic nonspecific low back pain.
Intervention: Patients allocated to the Kinesio Taping® group will receive the tape as
described by the manufacturer's manual. The patients assigned to the placebo group will
receive a Micropore tape and the control group will not receive any intervention. All groups
will be assessed before and 30 minutes after intervention
Measures: The following outcomes will be measured: 1) Muscle activity and 2) pain intensity.
Limitations: Therapists will not be blinded.
Status | Not yet recruiting |
Enrollment | 63 |
Est. completion date | February 2017 |
Est. primary completion date | October 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Patients with chronic low back pain (with a duration of at least 3 months), with or without leg pain. Exclusion Criteria: - patients who have used the Kinesio Taping previously - any contraindications to the use of Kinesio Tex Gold®, such as allergy or severe skin problems. - patients with nerve root compromise - patients with fracture, tumor, inflammatory and/or infectious diseases - patients with severe cardiorespiratory and/or metabolic diseases - previous spinal surgery |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Leandro Pires |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Disability | Disability will be measured with a 0-24 Roland Morris Disability Questionnaire. | baseline only | No |
Primary | Median Force | Median force (a measure of muscle activity) will be collected using surface electromyography. | thirty minutes after interventions | No |
Primary | Root Mean Square | Root Mean Square (a measure of muscle activity) will be collected using surface electromyography. | thirty minutes after interventions | No |
Secondary | Pain Intensity | This outcome will be measured using a 0-10 numerical rating scale ranging from "no pain" to "worse possible pain". | thirty minutes after interventions | No |
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