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Clinical Trials/NCT04170816
NCT04170816
Unknown
Not Applicable

Comparing Dry Needling With And Without Kinesio Taping® in The Treatment of Non-Specific Chronic Low Back Pain

Kars State Hospital0 sites60 target enrollmentDecember 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-Spesific Chronic Low Back Pain
Sponsor
Kars State Hospital
Enrollment
60
Primary Endpoint
Pain by visual analog scale (VAS)
Last Updated
6 years ago

Overview

Brief Summary

We wiil evaluate the efficiency of adding kinesio taping (KT) therapy to dry needling (DN) therapy on pain, functionality and depression parameters in 60 patients with nonspecific chronic low back pain (nCLBP).

Detailed Description

A total of 60 patients will be included in the study. 30 patients will be in the treatment group and 30 patients will be in the control group. Both groups will be underwent 3 sessions with 1-week intervals on active myofascial trigger points in lumbar multifidus, quadratus lumborum and gluteus medius muscles in DN therapy. KT application will be performed after every DN session in the study group. Pain will evaluate with visual analog scale, functionality was evaluated with Oswestry Disability Index and the status of depression will be evaluated with Beck Depression Index before the treatment and at the first month.

Registry
clinicaltrials.gov
Start Date
December 1, 2019
End Date
March 1, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Kars State Hospital
Responsible Party
Principal Investigator
Principal Investigator

Fatih Bagcier

Principal Investigator

Kars State Hospital

Eligibility Criteria

Inclusion Criteria

  • having no abnormal results in routine blood tests
  • having no known acute or chronic inflammatory disease
  • an education level required for understanding the applied treatment, interventions

Exclusion Criteria

  • malignancies
  • active infection
  • history of common inflammatory rheumatic disease
  • trauma in spinal area, skin lesion, presence of infection or open wounds
  • radiculopathy
  • peripheral circulation disorder
  • use of warfarin due to coagulopathy
  • arthropathy
  • congenital or acquired spinal pathology
  • pregnancy

Outcomes

Primary Outcomes

Pain by visual analog scale (VAS)

Time Frame: 3 week

Visual analog scale (VAS,0-10) will be used to assess resting, activity and night pain.

Beck Depression Inventory

Time Frame: 3 week

This is a 21-item standard assessment used to measure clinical depression. Scores on this assessment range from 0 to 63, where higher scores indicate higher levels of depression.

Pain pressure threshold

Time Frame: 3 week

Amount of pressure (Kg/cm2) applied at the lomber multifidus muscle, quadratus lumborum and gluteus medius muscle myofascial trigger point site that elicit pain for the patient will be reported

Oswestry disability Index (ODI)

Time Frame: 3 week

Changes from the Baseline, ODI is an effective tool to provide information on the extent of backache affecting the patient ability to cope with tasks of everyday life. Ten sections are included in the ODI tool with a total possible score of 5 for each section. The first statement carries a score of 0, and the last has a score of 5.

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