The Effect of Different Kinesio Taping Techniques Applied to Patients With Chronic Low Back Pain on the Thoracolumbar Fascia
1 other identifier
interventional
60
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable low-back-pain
Started Jan 2026
Shorter than P25 for not_applicable low-back-pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 15, 2025
CompletedFirst Posted
Study publicly available on registry
January 5, 2026
CompletedStudy Start
First participant enrolled
January 19, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2026
CompletedFebruary 27, 2026
February 1, 2026
3 months
December 15, 2025
February 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain intensity
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).
6 week
The thoracolumbar fascia thickness/ULTRASOUND
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).
6 week
Secondary Outcomes (7)
LOW BACK PAIN DISABILITY
6 week
Posture
6 week
Lateral Bridge Testt
6 week
Spinal Mobility:
6 week
Postural Endurance (Postural Competence):
6 week
- +2 more secondary outcomes
Study Arms (3)
Group 1 (Functional Fascial Taping Group):
EXPERIMENTALFor this group, "I" and "Y" kinesiology tape will be applied using a fascial correction technique on the thoracolumbar fascia with 10-50% oscillatory (oscillating) tension. The taping direction will be determined based on the direction in which pain is most reduced during movement.
Group 2 (Muscle Technique Taping Group):
ACTIVE COMPARATORThis group will be applied using "I" strip kinesiology tape muscle taping techniques on the paravertebral muscles. Two of the tapes will be applied completely tension-free (0%), while one will be applied transversely to the sacroiliac region with 25% tension.
Group 3 (Damascus Taping Group):
SHAM COMPARATORThis group will receive kinesiology tape applied symbolically to the skin over the thoracolumbar region without any therapeutic taping technique, without targeting fascia or muscle correction, and without creating meaningful tension (0% tension). Sham taping will be used to control for the placebo effect, independent of the specific mechanical and neurophysiological effects of taping.
Interventions
The treatment program for the Functional Fascial Taping Group is as follows: Participants in this group will undergo a targeted fascial correction technique applied to the thoracolumbar fascia. In practice, "I" and "Y" strips cut from 5 cm x 5 m kinesiology tape will be used, and the tapes will be applied to the right and left thoracolumbar fascia with an oscillatory (oscillating) tension in the range of 10-50%. The protocol will be repeated for a total of 2 weeks (4 sessions), twice a week, and the tapes will be replaced at each session. The primary goal is to reduce pain and improve function by directly affecting the biomechanics of the fascial tissue. Patients in the stabilization exercises group will perform cervical stabilization exercises consisting of 3 levels with gradually increasing difficulty. The exercises will be taught to patients level by level by a physical therapist over 6 weeks. Stretching exercises will be performed before each exercise session.
In this group, the more traditional approach of muscle taping will be adopted. The application will be performed using three "I"-shaped strips of tape. The first two strips will be placed completely tension-free (0%) on the paravertebral muscles while the patient is leaning forward and performing a slight rotation. The third tape will be applied transversally with 25% tension, parallel to the ground, over the sacroiliac joints. This protocol will also be applied twice a week for two weeks, with the aim of providing muscle support and increasing stabilization.
The taping applied in this group will not aim to correct any muscles or fascia, will be performed without applying therapeutic tension (0% tension), and will not produce a standard clinical effect. At the end of the study, all participants will be informed that they can access known effective taping approaches upon request.
Patients in the stabilization exercise group will be given cervical stabilization exercises consisting of 3 levels with gradually increasing difficulty. The exercises will be taught to patients level by level by a physical therapist over 6 weeks. Patients will perform the exercises for a total of 6 weeks. Patients will be asked to perform stretching exercises before each exercise session.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
- Recent Treatments: Having undergone a physical therapy and rehabilitation (PTR) program targeting the lumbar region or an intervention such as an injection within the last 3 months prior to the start of the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kirşehir Ahi Evran Univercity
Center, Kirşehi̇r, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Şafak KUZU
Kirsehir Ahi Evran Universitesi
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assist. Prof.
Study Record Dates
First Submitted
December 15, 2025
First Posted
January 5, 2026
Study Start
January 19, 2026
Primary Completion
May 1, 2026
Study Completion
May 15, 2026
Last Updated
February 27, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share