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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02550457
Other study ID # 056666/2015
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2015
Est. completion date March 2017

Study information

Verified date May 2018
Source Universidade Federal do Rio Grande do Norte
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study propose analyze the effects of Kinesio Taping® in chronic nonspecific low back pain. All the subjects will be submitted to an evaluation of the painful sensation, functional performance, trunk range of motion and neuromuscular performance at three different times.


Recruitment information / eligibility

Status Completed
Enrollment 108
Est. completion date March 2017
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Female between 18 and 50 years of age with chronic nonspecific low back pain for more than three months.

Exclusion Criteria:

- Serious spinal pathologies (fractures, tumors, and inflammatory pathologies such as ankylosing spondylitis);

- Nerve root compromise (disc herniation and spondylolisthesis with neurological compromise, spinal stenosis, and others);

- Fibromyalgia

- Corticosteroid treatment in the previous two weeks;

- Antiinflammatory treatment in the previous 24 hours;

- Contraindications to the use of Kinesio Taping (allergy or intolerance);

- Score of two or less on Visual Analogue Scale of the first day;

- Pregnancy;

- Previous Kinesio Tape therapy on lumbar.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Functional elastic tape tensioned
Application of Kinesio Taping with tension in the erector spine muscles.
Functional elastic tape non-tensioned
Application of Kinesio Taping without tension in the erector spine muscles.
Rigid Tape
Application of Micropore tape in the erector spine muscles.

Locations

Country Name City State
Brazil Universidade Federal do Rio Grande do Norte Natal Rio Grande Do Norte

Sponsors (1)

Lead Sponsor Collaborator
Universidade Federal do Rio Grande do Norte

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Painful sensation Pain sensation measured by pain numerical rating scale Evaluation of pain sensation three days after the application of the tape.
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