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Clinical Trials/NCT05203783
NCT05203783
Completed
Not Applicable

Short-term Effects of Kinesio Taping in Patients With Mechanical Low Back Pain: A Randomized Clinical Trial.

Marmara University1 site in 1 country30 target enrollmentAugust 8, 2021
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Marmara University
Enrollment
30
Locations
1
Primary Endpoint
Visual analogue scale (VAS)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The aim of this study is to estimate the effect of Kinesio tape (KT) combined with supervised exercise programs compared to exercise alone on pain, lumbar range of motion, and self-reported disability of adults with mechanical low back pain (LBP).

Methods: This was a randomized, controlled clinical trial carried out on 60 individuals with mechanical LBP. Participants were randomly assigned to the control group (n=30) that received McKenzie exercises for 7 days or experimental group (n=30) that received KT application in addition to McKenzie exercises for 7 days. Pain measured by visual analogue scale, lumbar range of motion, and the disability measured by Oswestry Disability Index (ODI) were used as outcome measures. Pre and Post measurements were taken at baseline and after 7 days.

Registry
clinicaltrials.gov
Start Date
August 8, 2021
End Date
December 25, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Eren Timurtas

Principal Investigator

Marmara University

Eligibility Criteria

Inclusion Criteria

  • Individuals diagnosed with mechanical LBP by a physician

Exclusion Criteria

  • Individuals with any structural or pathological changes (spondylitis, spondylolisthesis, cauda equina syndrome, lumbar canal stenosis) in lumbar spine on X-ray or MRI
  • Individuals with or without neurological signs in the lower extremity suggestive upper motor or lower motor neuron involvement,
  • Individuals with a history of trauma or any surgery in the region of back,
  • Individuals with recent aggravation of symptoms,
  • Individuals on a waiting list for spinal surgery or had a spinal surgery in the past 6 months

Outcomes

Primary Outcomes

Visual analogue scale (VAS)

Time Frame: The pain was measured at the end of intervention (7th day).

Pain was measured using a 10 cm visual analogue scale (VAS). The participants placed a mark on the line that best represented their perception of pain at that instant. The VAS score was measured in cm from the left hand end of the line to the mark.

Secondary Outcomes

  • The Oswestry Disability Index (ODI)(The ODI was measured at the end of intervention (7th day) 2 minutes after the pain assesment.)

Study Sites (1)

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