NCT07425301

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
102

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2024

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

November 3, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 10, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 2, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

February 13, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 20, 2026

Completed
Last Updated

February 20, 2026

Status Verified

February 1, 2026

Enrollment Period

10 months

First QC Date

February 13, 2026

Last Update Submit

February 13, 2026

Conditions

Keywords

Chronic Low Back PainKinesiological TapingConservative TreatmentIschemic Compression

Outcome Measures

Primary Outcomes (1)

  • Change in Pain Intensity (Visual Analog Scale)

    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.

    Baseline and after completion of the 3-week intervention period

Secondary Outcomes (4)

  • Change in Lumbar Flexion Range of Motion

    Baseline and after completion of the 3-week intervention period

  • Change in Lumbar Extension Range of Motion

    Baseline and after completion of the 3-week intervention period

  • Change in Lumbar Right Lateral Flexion Range of Motion

    Baseline and after completion of the 3-week intervention period

  • Change in Lumbar Left Lateral Flexion Range of Motion

    Baseline and after completion of the 3-week intervention period

Study Arms (3)

Conventional Treatment Group

ACTIVE COMPARATOR

Participants in this group receive conventional treatment consisting of standard physiotherapy modalities administered according to a structured treatment protocol over a three-week period. No additional taping or manual compression techniques are applied in this group.

Other: Conventional Physiotherapy Program

Conventional Treatment Plus Kinesiology Taping Group

EXPERIMENTAL

Participants in this group receive conventional treatment consisting of standard physiotherapy modalities together with kinesiology taping applied according to a structured application protocol over a three-week treatment period.

Procedure: Kinesiology Taping

Conventional Treatment Plus Ischemic Compression Group

EXPERIMENTAL

Participants in this group receive conventional treatment consisting of standard physiotherapy modalities together with ischemic compression therapy applied according to a structured protocol during scheduled sessions over a three-week period.

Procedure: Ischemic Compression Therapy

Interventions

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.

Conventional Treatment Plus Ischemic Compression Group

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

Conventional Treatment Group

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

Conventional Treatment Plus Kinesiology Taping Group

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Inonu University Turgut Ozal Medical Center

Malatya, 4400, Turkey (Türkiye)

Location

Study Officials

  • Ilker Demir, PhD

    Inonu University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants are assigned to one of three parallel groups: a conventional treatment group, a conventional treatment plus kinesiology taping group, or a conventional treatment plus ischemic compression group. All groups are followed over the same study period, and outcomes are assessed before and after the intervention to compare changes among groups.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Inonu Universty

Study Record Dates

First Submitted

February 13, 2026

First Posted

February 20, 2026

Study Start

November 3, 2024

Primary Completion

September 10, 2025

Study Completion

December 2, 2025

Last Updated

February 20, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared because data sharing was not included in the study protocol and no data-sharing agreement or repository plan was established.

Locations