Ischemic Compression and Home Exercise in Non-Specific Neck Pain

Sponsor
Istanbul Rumeli University
Study ID
NCT07685418
Status
Recruiting
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Conditions

  • Musculoskeletal Pain
  • Myofascial Trigger Points
  • Neck Pain
  • Non-specific Neck Pain

Eligibility Criteria

Sex
ALL
Age
17 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • Ischemic Compression — OTHER
    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
  • Home Exercise Program — OTHER
    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.

Study Details

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.

Key Dates

First listed
Jul 6, 2026
Start date
May 13, 2026
Status verified
Jun 2026
Primary completion
Jun 30, 2026
Completion
Jul 15, 2026

Study Design

Enrollment
52 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Experimental Group
    Ischemic compression will be applied to painful points in the neck region. Pressure will be applied until the patient's pain threshold is reached and maintained for a specific duration.
  • Active Comparator: Control Group
    Participants will perform a structured home exercise program consisting of stretching and strengthening exercises for the cervical region.

Primary Outcome Measure

Pain Intensity [ Time Frame: Baseline and post-treatment (week 4) ]

Central Contacts

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