Kinesio Taping for Balance and Function in Low Back Pain (KTFB-NSLBP)

June 24, 2025 updated by: Elif Dilara Durmaz

A Randomized Controlled Trial on the Effect of Kinesio Taping on Balance and Functionality in Patients With Nonspecific Low Back Pain

This study aims to examine the effects of kinesiology taping on balance and functional ability in individuals with nonspecific low back pain. Nonspecific low back pain is a common condition that is not linked to a specific medical cause and is often associated with balance problems, reduced physical function, and psychological challenges. In this study, 35 patients aged between 18 and 65 were included. One group received kinesiology taping along with physiotherapy, while the other group received only physiotherapy.

Study Overview

Status

Completed

Detailed Description

Nonspecific low back pain (NSLBP) is a common musculoskeletal condition that cannot be attributed to a specific pathology. It often leads to limitations in functional activities, impaired balance, and psychological distress, such as depressive symptoms. This study investigates the effects of kinesiology taping on balance and functional outcomes in individuals diagnosed with NSLBP.

The study was conducted on 35 participants aged 18 to 65 years. Participants were randomly assigned to two groups: the intervention group received kinesiology taping in combination with physiotherapy, while the control group received only physiotherapy treatment. Various outcome measures were used to assess the effects of the interventions, including the Visual Analog Scale (VAS) for pain intensity, Functional Rating Index (FRI), Modified Oswestry Disability Index (MODI), Beck Depression Inventory (BDI), Nottingham Health Profile (NHP), and the Flamingo Balance Test.

Study Type

Interventional

Enrollment (Actual)

35

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey
        • Istinye Universyt

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients aged between 18 and 65 years
  • Diagnosis of nonspecific low back pain
  • Duration of low back pain longer than 6 weeks
  • Ability to attend an outpatient physiotherapy program

Exclusion Criteria:

  • History of spinal surgery
  • Presence of neurological deficits on physical examination
  • Contraindication to kinesiology taping
  • Pregnancy
  • Cardiovascular or pulmonary diseases that contraindicate exercise
  • History of lower extremity surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Kinesiology Taping + Physiotherapy
Participants in this group received kinesiology taping applied to the lumbar region in addition to a physiotherapy program that included therapeutic exercises and modalities tailored for nonspecific low back pain. The intervention aimed to improve balance, reduce pain, and enhance functional outcomes.
Kinesiology taping was applied to the lumbar area of the participants in the intervention group. The taping aimed to improve posture, reduce pain, and enhance balance and functional performance.
The physiotherapy program included therapeutic exercises and physical modalities (such as stretching, strengthening, and posture training) tailored for individuals with nonspecific low back pain.
Active Comparator: Physiotherapy Only
Participants in this group received only the physiotherapy program, which included therapeutic exercises and modalities commonly used in the treatment of nonspecific low back pain. No kinesiology taping was applied in this group.
The physiotherapy program included therapeutic exercises and physical modalities (such as stretching, strengthening, and posture training) tailored for individuals with nonspecific low back pain.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Functional Rating Index (FRI) score
Time Frame: Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Functional status was assessed using the Functional Rating Index (FRI) to evaluate the level of functional disability related to nonspecific low back pain. A decrease in the score indicates improved functional status.
Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Visual Analog Scale (VAS) score for pain
Time Frame: Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Pain intensity was evaluated using the Visual Analog Scale. A decrease in score indicates reduced pain severity.
Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Change in Flamingo Balance Test (FBT) score
Time Frame: Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Balance was assessed using the Flamingo Balance Test. Improved performance indicates better postural control and balance.
Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Change in Beck Depression Inventory (BDI) score
Time Frame: Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Psychological status was assessed using the Beck Depression Inventory. A decrease in score reflects improved mood and reduced depressive symptoms.
Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Change in Oswestry Disability Index (ODI) score
Time Frame: Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Disability level related to low back pain was evaluated using the Oswestry Disability Index. A decrease in score reflects improved functional ability.
Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Change in Nottingham Health Profile (NHP) score
Time Frame: Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)
Health-related quality of life was evaluated using the Nottingham Health Profile. A decrease in score indicates better quality of life.
Baseline (Day 1)": Initial assessment (Day 1 of the study) "3 weeks post-intervention": Second assessment, 3 weeks after the intervention (after the treatment program)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 20, 2025

Primary Completion (Actual)

June 15, 2025

Study Completion (Actual)

June 20, 2025

Study Registration Dates

First Submitted

March 19, 2025

First Submitted That Met QC Criteria

April 20, 2025

First Posted (Actual)

April 25, 2025

Study Record Updates

Last Update Posted (Actual)

June 26, 2025

Last Update Submitted That Met QC Criteria

June 24, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ISU_NSLBP_KT_2025

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Low Back Pain

Clinical Trials on Kinesiology Taping

Subscribe