- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06945783
Kinesio Taping for Balance and Function in Low Back Pain (KTFB-NSLBP)
A Randomized Controlled Trial on the Effect of Kinesio Taping on Balance and Functionality in Patients With Nonspecific Low Back Pain
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey
- Istinye Universyt
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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 |
|---|---|
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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.
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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.
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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.
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The physiotherapy program included therapeutic exercises and physical modalities (such as stretching, strengthening, and posture training) tailored for individuals with nonspecific low back pain.
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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)
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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.
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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)
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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)
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Pain intensity was evaluated using the Visual Analog Scale.
A decrease in score indicates reduced pain severity.
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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)
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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)
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Balance was assessed using the Flamingo Balance Test.
Improved performance indicates better postural control and balance.
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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)
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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)
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Psychological status was assessed using the Beck Depression Inventory.
A decrease in score reflects improved mood and reduced depressive symptoms.
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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)
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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)
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Disability level related to low back pain was evaluated using the Oswestry Disability Index.
A decrease in score reflects improved functional ability.
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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)
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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)
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Health-related quality of life was evaluated using the Nottingham Health Profile.
A decrease in score indicates better quality of life.
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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)
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
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