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Clinical Trials/NCT04039581
NCT04039581
Completed
Not Applicable

Short-Term Effects of Kinesio Taping® on Pain and Functionality in Patients with Cervical Spine Surgery

Marmara University1 site in 1 country90 target enrollmentOctober 19, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Marmara University
Enrollment
90
Locations
1
Primary Endpoint
Pain Intensity
Status
Completed
Last Updated
last year

Overview

Brief Summary

Aim of the study was to investigate the effect of Kinesio taping application on upper trapezius muscle after cervical spine surgery.

Detailed Description

Patients will be randomly divided into three groups. The first group will receive conservative treatment and Kinesio Taping application. The second group will receive conservative treatment and the third group will receive only Kinesio taping application. The treatment procedure will continue for post-operatively three days and assessments will be done four times; before the surgery, post-operative 1st day, postoperative 3rd day and two weeks after surgery. Data will be recorded on patient assessment file and transferred to the computer. Data analysis will be performed with SPSS.22.

Registry
clinicaltrials.gov
Start Date
October 19, 2019
End Date
December 30, 2020
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • To be voluntary participation in the study,
  • Aged 25-75 years old,
  • To be diagnosed with cervical disc herniation, cervical stenosis and cervical spondylolisthesis
  • No mental problem, sensory or motor aphasia in order to understand and answer the evaluation questions correctly.

Exclusion Criteria

  • History of surgery,
  • Allergic reaction to kinesio taping,
  • Primary or metastatic neoplasm in cervical spine,
  • History of different treatment for neck pain during the study period,
  • Individuals with any congenital deformity in the spine,
  • Having any rheumatologic, neurological and orthopedic disease.

Outcomes

Primary Outcomes

Pain Intensity

Time Frame: Change from baseline to two weeks after the surgery

Neck pain intensity will be assessed with Visual Analog Scale (VAS).The VAS is usually a horizontal line, 10 cm in length, anchored by word descriptors at each end with "No Pain" (score of zero) on the left side up to "pain as bad as it could be" or the "worst imaginable pain" (Score of 100 \[100-mm scale\]) on the right side.The patient was asked to mark the line point that represented his or her current pain.

Pain pressure threshold

Time Frame: Change from baseline to two weeks after the surgery

Pain pressure threshold of the trapezius muscle will be evaluated by digital pressure algometry. In the process, three measurements will be taken and the average value will be taken as reference.

Secondary Outcomes

  • Functionality Score(Change from baseline to two weeks after the surgery)
  • Disability(Change from baseline to two weeks after the surgery)
  • Health Related Quality of Life Score(Change from baseline to two weeks after the surgery)
  • Range of Motion (ROM)(Change from baseline to two weeks after the surgery)

Study Sites (1)

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