Skip to main content
OpenTrials
Completed

NCT Number: NCT07425301

Comparing the Effects of Ischemic Compression and Kinesiology Taping Techniques

This study evaluates the effects of ischemic compression and kinesiology taping techniques on pain intensity and lumbar range of motion in individuals with chronic low back pain. Participants are assigned to one of three groups: a conventional treatment group, a conventional treatment plus kinesiology taping group, or a conventional treatment plus ischemic compression group. Interventions are administered over a three-week period. Outcome measures are assessed before and after the intervention using standardized assessment methods. The purpose is to compare changes among groups and examine the effects of adding these techniques to conventional treatment.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Chronic Low Back Pain

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Inonu University Turgut Ozal Medical Center

Malatya, 4400, Turkey (Türkiye)

About this study

Chronic low back pain is a common musculoskeletal condition associated with pain, reduced mobility, and functional limitations. Nonpharmacological interventions are frequently used to support symptom management and improve physical function. Manual therapy techniques and supportive therapeutic applications are commonly included in rehabilitation programs for individuals with chronic low back pain.

This study is designed to investigate the effects of ischemic compression and kinesiology taping techniques in individuals with chronic low back pain. Participants are assigned to different intervention groups receiving either conventional treatment alone or conventional treatment combined with additional therapeutic techniques. Interventions are delivered according to structured protocols over a defined treatment period. Outcome measures evaluate changes in pain intensity and lumbar range of motion using standardized assessment methods.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Volunteers willing to participate in the study,
  • Those who have had back pain for at least 12 weeks,
  • Those who have been tested with a test patch and have no allergy to kinesiology tape,
  • Patients who can comply with the exercise programme to be applied were included in the study.

Exclusion criteria

  • Patients who have undergone surgery for back pain,
  • Pregnant women,
  • Patients with rheumatological diseases were not included in the study.

Treatment and study plan

Conventional Physiotherapy Program

Other

Conventional treatment consists of standard physiotherapy modalities administered according to a structured protocol during scheduled sessions over a three-week period.

Kinesiology Taping

Procedure

Kinesiology taping is applied using standardized techniques by a trained therapist according to a structured application protocol during the treatment period.

Ischemic Compression Therapy

Procedure

Ischemic compression therapy is a manual technique applied by a therapist using sustained pressure to targeted areas according to a structured treatment protocol during scheduled sessions.

Primary outcomes

  1. Change in Pain Intensity (Visual Analog Scale)

    Time frame: Baseline and after completion of the 3-week intervention period

    Pain intensity is assessed using the Visual Analog Scale, a validated measure consisting of a scale ranging from no pain to worst imaginable pain. Change is calculated as the difference between pre-intervention and post-intervention scores.

Secondary outcomes

  1. Change in Lumbar Flexion Range of Motion

    Time frame: Baseline and after completion of the 3-week intervention period

    Lumbar range of motion is assessed using standardized measurement methods to evaluate spinal mobility. Measurements are obtained before and after the intervention, and change is calculated as the difference between pre-intervention and post-intervention values.

  2. Change in Lumbar Extension Range of Motion

    Time frame: Baseline and after completion of the 3-week intervention period

    Lumbar range of motion is assessed using standardized measurement methods to evaluate spinal mobility. Measurements are obtained before and after the intervention, and change is calculated as the difference between pre-intervention and post-intervention values.

  3. Change in Lumbar Right Lateral Flexion Range of Motion

    Time frame: Baseline and after completion of the 3-week intervention period

    Lumbar range of motion is assessed using standardized measurement methods to evaluate spinal mobility. Measurements are obtained before and after the intervention, and change is calculated as the difference between pre-intervention and post-intervention values.

  4. Change in Lumbar Left Lateral Flexion Range of Motion

    Time frame: Baseline and after completion of the 3-week intervention period

    Lumbar range of motion is assessed using standardized measurement methods to evaluate spinal mobility. Measurements are obtained before and after the intervention, and change is calculated as the difference between pre-intervention and post-intervention values.

Sponsors and collaborators

Lead sponsor

Hasan Kalyoncu University

Other

Registry information

Official study title

Comparing the Effects of Ischemic Compression and Kinesiology Taping Techniques in Patients With Chronic Low Back Pain

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Feb 20, 2026
Registry last updated
Feb 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.