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Clinical Trials/NCT07317518
NCT07317518
Not yet recruiting
Not Applicable

The Effect of Different Kinesio Taping Techniques Applied to Patients With Chronic Low Back Pain on the Thoracolumbar Fascia: A Randomized Controlled Trial

Kirsehir Ahi Evran Universitesi0 sites60 target enrollmentStarted: January 15, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Kirsehir Ahi Evran Universitesi
Enrollment
60
Primary Endpoint
Pain intensity

Overview

Brief Summary

This study aims to evaluate the effects of functional thoracolumbar fascia kinesiology taping on fascia thickness, pain, and functional disability in individuals with nonspecific chronic low back pain. The study is planned as a randomized controlled trial and will include a total of 30 individuals aged 18-65 years who have been diagnosed with nonspecific mechanical chronic low back pain. Participants will be randomly assigned to two groups: the Functional Fascial Taping Group will receive kinesiology tape applied to the thoracolumbar fascia using a fascia correction technique, while the Muscle Technique Taping Group will receive traditional muscle taping applied to the paravertebral muscles. Interventions will be performed twice a week for two weeks. Assessments will be performed before and after treatment; pain intensity will be measured using the Visual Analog Scale, pressure pain threshold will be measured using an algometer, functional disability will be measured using the Oswestry Low Back Pain Disability Index, and thoracolumbar fascia thickness will be measured using ultrasonography. The findings are expected to contribute to clinical practice by providing evidence-based data on the effectiveness of different kinesiology taping techniques in chronic low back pain.

Detailed Description

Non-specific chronic low back pain is a highly prevalent musculoskeletal condition associated with recurrent symptoms, functional limitations, and substantial psychosocial burden. Current clinical practice frequently relies on passive treatment approaches, including various taping techniques; however, the specific effects of different kinesio taping methods on fascial structures remain insufficiently explored. In particular, objective evidence regarding changes in thoracolumbar fascia morphology following targeted taping interventions is limited.

This randomized controlled study aims to compare the effects of functional fascial kinesio taping and conventional muscle taping on thoracolumbar fascia thickness, pain perception, and functional disability in individuals with non-specific chronic low back pain. Participants diagnosed with non-specific mechanical chronic low back pain will be randomly allocated to one of two intervention groups. One group will receive functional fascial taping applied according to movement-based pain modulation principles, while the comparison group will receive traditional muscle-oriented kinesio taping. Both interventions will be administered over a short-term treatment period without additional therapeutic modalities to isolate the effects of taping.

Outcome assessment will focus on changes in pain intensity, pressure pain sensitivity, functional disability, and thoracolumbar fascial characteristics. Fascial thickness will be evaluated using ultrasonographic imaging to provide an objective measure of tissue-level response. By integrating subjective clinical outcomes with imaging-based assessment, this study seeks to clarify whether taping strategies that target fascial mechanics offer advantages over conventional muscle-focused approaches.

The findings are expected to contribute to evidence-based decision-making in rehabilitation practice by informing clinicians about the potential role of fascia-oriented taping in the management of chronic low back pain, while minimizing redundancy with procedural and technical details documented elsewhere in the study record.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age: Be between 18 and 65 years old.
  • Volunteer status: Be willing to participate in the study and sign an informed consent form.
  • Diagnosis: Have been diagnosed by a physician with nonspecific mechanical chronic low back pain. This diagnosis is defined as follows:
  • A pain episode lasting longer than 6 weeks or
  • A history of recurrent low back pain (episodes lasting longer than 24 hours with at least one pain-free period of one month before/after the episode).
  • Localization: Pain localized between the lowest rib and the gluteal folds.

Exclusion Criteria

  • Specific Spinal Pathologies: The presence of a specific cause for back pain (e.g., structural abnormalities such as herniation, stenosis, spondylolisthesis).
  • History of Major Trauma: A history of serious trauma to the back region.
  • Systemic Diseases: Systemic diseases that may affect the outcome, such as rheumatological diseases or diabetes.
  • History of Cancer: Any cancer diagnosis or history.
  • Osteoporosis: Diagnosis of bone loss.
  • Inflammatory or Neurological Diseases: Diagnosis of inflammatory rheumatic diseases such as ankylosing spondylitis or a neurological disease.
  • Radicular Pain: Presence of radicular pain radiating to the legs, suggesting nerve root compression.
  • Skin Conditions:
  • Known skin sensitivity or allergy to the patches.
  • Active dermatitis or pre-existing skin lesion in the patch application area.

Outcomes

Primary Outcomes

Pain intensity

Time Frame: 6 week

The Visual Analog Scale (VAS) will be used to measure participants' pain intensity. Participants are asked to indicate their current state by placing a line or dot on a 10-centimeter straight line, where both ends are defined by the parameter to be measured in the individual. Pain intensity in the individual is calculated in this way. For example, the parameters to be evaluated are determined at one end of the drawn 10-centimeter straight line (0 = no pain, 10 = unbearable pain).

The thoracolumbar fascia thickness/ULTRASOUND

Time Frame: 6 week

The thoracolumbar fascia thickness will be measured using the Versana Primer R2 VS GE (China, 2022) ultrasound with a 4.0-13.0 MHz, 38.4 mm probe and a scanning protocol performed at the L3 level of the lumbar spine. Measurements will be performed by an experienced physician doctor in musculoskeletal ultrasound. Measurements will be performed bilaterally in the standard manner, with the patient lying comfortably in the prone position. Measurements will be performed using ultrasound B-mode and a depth setting of 30 mm. Sufficient gel will be used to avoid probe compression on the skin to ensure accurate measurements. To prevent TLF thickness differences from affecting the results, measurements will be taken at 3 separate points and averaged. As recommended by Pirri et al., the probe will be placed perpendicularly, and short and long axis images will be obtained. Images will be recorded and measurements will be taken (Pirri et al., 2024).

Secondary Outcomes

  • LOW BACK PAIN DISABILITY(6 week)
  • Posture(6 week)
  • Lateral Bridge Testt(6 week)
  • Spinal Mobility:(6 week)
  • Postural Endurance (Postural Competence):(6 week)
  • Static Trunk Extension Test (Sorensen Test):(6 week)
  • Trunk Flexor Endurance Test(6 week)

Investigators

Sponsor
Kirsehir Ahi Evran Universitesi
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Safak Kuzu

Assist. Prof.

Kirsehir Ahi Evran Universitesi

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