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

Not Applicable

Completed

• Conditions: Low Back Pain

• Registration Number: NCT05015842
• Lead Sponsor: NCS University System

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.

Study Timeline

• Study Start: 2019-01-02
• Primary Completion: 2019-04-11
• Study Completion: 2019-06-03
• Status Verified: 2021-08
• Study First Submitted: 2021-08-13
• Study First Submitted QC: 2021-08-19
• Last Update Submitted: 2021-08-19
• Study First Posted: 2021-08-20
• Last Update Posted: 2021-08-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 56

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Pain intensity	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 Outcome Measures

Name	Time	Method
Functional Disability	2 weeks	Functional disability was measured using Oswestry Disability Index (ODI. ODI score was converted to percentage so the score ranges from 0% to 100%. Where 0% mean no disability and 100 mean very severe (maximum) disability. The minimum score mean better outcome while higher score mean worse outcome. simply lesser the score better would be the outcome.

Trial Locations

Locations (1)

NCS University System, Department of Physical Therapy and Rehabilitation; 🇵🇰 Peshawar, Khyber Pakhtunkhwa, Pakistan