Comparing the Effects of Ischemic Compression and Kinesiology Taping Techniques
1 other identifier
interventional
102
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2024
1 active site
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
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 10, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 2, 2025
CompletedFirst Submitted
Initial submission to the registry
February 13, 2026
CompletedFirst Posted
Study publicly available on registry
February 20, 2026
CompletedFebruary 20, 2026
February 1, 2026
10 months
February 13, 2026
February 13, 2026
Conditions
Keywords
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 COMPARATORParticipants 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.
Conventional Treatment Plus Kinesiology Taping Group
EXPERIMENTALParticipants 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.
Conventional Treatment Plus Ischemic Compression Group
EXPERIMENTALParticipants 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.
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 consists of standard physiotherapy modalities administered according to a structured protocol during scheduled sessions over a three-week period.
Kinesiology taping is applied using standardized techniques by a trained therapist according to a structured application protocol during the treatment period.
Eligibility Criteria
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)
Study Officials
- PRINCIPAL INVESTIGATOR
Ilker Demir, PhD
Inonu University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- 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.