NCT07317518

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

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P50-P75 for not_applicable low-back-pain

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable low-back-pain

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 15, 2025

Completed
21 days until next milestone

First Posted

Study publicly available on registry

January 5, 2026

Completed
14 days until next milestone

Study Start

First participant enrolled

January 19, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2026

Completed
Last Updated

February 27, 2026

Status Verified

February 1, 2026

Enrollment Period

3 months

First QC Date

December 15, 2025

Last Update Submit

February 25, 2026

Conditions

Keywords

Non-specific chronic low back painKinesio tapingThoracolumbar fascia

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):

EXPERIMENTAL

For 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.

Other: Functional Fascial Taping GroupOther: Traditional treatment

Group 2 (Muscle Technique Taping Group):

ACTIVE COMPARATOR

This 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.

Other: Muscle Technique Taping GroupOther: Traditional treatment

Group 3 (Damascus Taping Group):

SHAM COMPARATOR

This 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.

Other: Damascus Banding GroupOther: Traditional treatment

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.

Group 1 (Functional Fascial Taping Group):

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.

Group 2 (Muscle Technique Taping Group):

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.

Group 3 (Damascus Taping Group):

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.

Group 1 (Functional Fascial Taping Group):Group 2 (Muscle Technique Taping Group):Group 3 (Damascus Taping Group):

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

RECRUITING

MeSH Terms

Conditions

Low Back Pain

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Şafak KUZU

    Kirsehir Ahi Evran Universitesi

    STUDY DIRECTOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized controlled trials
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

Locations