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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02007668
Other study ID # CAAE:16832013.9.0000.5512
Secondary ID
Status Completed
Phase N/A
First received November 30, 2013
Last updated December 5, 2013
Start date August 2013
Est. completion date November 2013

Study information

Verified date December 2013
Source Paulista University
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date November 2013
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility 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 Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Kinesio Taping
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.

Locations

Country Name City State
Brazil Universidade Paulista - UNIP Jundiaí São Paulo

Sponsors (1)

Lead Sponsor Collaborator
Paulista University

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Intensity Pain Intensity will be measured in 2 and 7 days after randomization by an 11-point (0-10) Numerical Rating Scale (Pain NRS) 2 days No
Secondary Disability 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 No
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