RecruitingNot ApplicableNCT07685418

Ischemic Compression and Home Exercise in Non-Specific Neck Pain

Evaluation of the Effects of Ischemic Compression Combined With Home Exercise on Pain Intensity and Quality of Life in Individuals With Chronic Non-Specific Neck Pain


Sponsor

Istanbul Rumeli University

Enrollment

52 participants

Start Date

May 13, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to investigate the effects of ischemic compression combined with home exercise on pain, cervical range of motion, neck disability level, and quality of life in individuals with non-specific neck pain. Participants will be divided into two groups: a treatment group receiving ischemic compression plus home exercises, and a control group receiving only home exercises. The study aims to provide clinical evidence regarding the effectiveness of combined treatment approaches for non-specific neck pain.


Eligibility

Min Age: 17 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Home Exercise Program and Ischemic Compression for people with musculoskeletal pain, neck pain, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 17 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERIschemic Compression

The intervention group will receive ischemic compression applied to palpable trigger points in the upper trapezius, middle trapezius, levator scapulae, suboccipital muscles (rectus capitis posterior major/minor, obliquus capitis), and splenius capitis muscles for 90 seconds with gradually increasing pressure at the individual's pain tolerance threshold. Ischemic compression will be performed by the therapist applying perpendicular, controlled, and gradually increasing pressure to the trigger point using the thumb or an appropriate contact surface. The pressure will be maintained at the participant's tolerable pain threshold (uncomfortable but bearable) and sustained for approximately 90 seconds per trigger point. Participant feedback will be obtained during the application; in cases of excessive pain or discomfort, the pressure will be reduced or the application will be terminated. The aim of the application is to reduce local tenderness at the trigger point, regulate muscle tone, and

OTHERHome Exercise Program

Participants will perform a structured program consisting of stretching and strengthening exercises for the cervical region. The program will be performed twice daily for the duration of the study.


Locations(1)

SZ Clinic Physical Therapy, Dietetics and Health Services Center

Istanbul, Bakırköy, Turkey (Türkiye)

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NCT07685418


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