Clinical Trial

Comparison of Three Different Myofascial Trigger Point Treatments in Chronic Non-Specific Neck Pain

Enrolling by Invitation
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Record status
This record was last updated February 7, 2025 (before its estimated December 15, 2025 completion). Its status may not reflect the trial's current state.
Summary
The aim of this study was to compare the efficacy of ischaemic compression (IC), positional relaxation (Strain Counterstrain \[SCS\]), and integrated neuromuscular inhibition technique (INIT) applications on pain intensity, pressure pain threshold, range of motion, joint position sense, disability, kinesiophobia, quality of life and patient satisfaction in addition to conventional treatment for chronic non-specific neck pain. It is planned to include 51 patients in the study. The included patients will be divided into 3 groups: Group 1 (HR Group), Group 2 (SCS Group) and Group 3 (INIT Group). All three groups will receive a conventional physiotherapy programme 5 times a week for 4 weeks and the same exercise programme 3 days a week for 4 weeks.
Trial Details
NCT Number NCT06814808
Lead Sponsor Biruni University
Conditions Chronic Non-specific Neck Pain
Enrollment 51 participants
Start Date 2024-12-15
Primary Completion 2025-12-15 (estimated)
Study Completion 2025-12-15 (estimated)
Updated on ClinicalTrials.gov 2025-02-07