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Clinical Trials/NCT05015842
NCT05015842
Completed
Not Applicable

Effectiveness of Kinesio Tapping for the Treatment of Patients With Acute Low Back Pain: A Randomized Control Trial

NCS University System1 site in 1 country56 target enrollmentJanuary 2, 2019
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
NCS University System
Enrollment
56
Locations
1
Primary Endpoint
Pain intensity
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The objective of the study was to determine the effectiveness of Kinesio Taping (KT) for the treatment of patients with acute low back pain.

In this study a total of 56 patients with acute low back pain were randomly allocated to the experimental group, KT along with conventional Physical therapy (PT), or the control group, conventional PT alone.

Detailed Description

The objective of the study was to determine the effectiveness of Kinesio Taping (KT) for the treatment of patients with acute low back pain. In this study a total of 56 patients with acute low back pain were randomly allocated to the experimental group, KT along with conventional Physical therapy (PT), or the control group, conventional PT alone. 28 Patients received KT in addition to conventional PT while 28 patients received conventional PT alone for two weeks. Oswestry disability index (ODI) and numeric pain rating scale (NPRS) were used for the measurement of outcomes.

Registry
clinicaltrials.gov
Start Date
January 2, 2019
End Date
June 3, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hazrat Bilal PT

Assistant Professor

NCS University System

Eligibility Criteria

Inclusion Criteria

  • Both Genders
  • Age between 18 and 60 years
  • History of LBP less than

Exclusion Criteria

  • Patients having diagnosed conditions of spondylolisthesis, spondylosis, lumbar stenosis, spinal tumor, lumber fracture, renal disease and trauma were excluded from the study.
  • Patients either with chronic LBP (duration more than 3 months) or contraindicated to KT (skin allergy or pre-existing skin lesion or infection) were also excluded.
  • Female Pregnant patients were also excluded from the study.

Outcomes

Primary Outcomes

Pain intensity

Time Frame: 2 weeks

Pain was measured on numerical pain rating scale. it is a scale with score from 0 to 10 where 0 is no pain and 10 is maximum pain. The minimum score mean better outcome while higher score mean worse outcome. simply lesser the score better would be the outcome.

Secondary Outcomes

  • Functional Disability(2 weeks)

Study Sites (1)

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