Actively Recruiting

Phase Not Applicable
Age: 30Years - 50Years
All Genders
NCT07413770

Comparison of Treatment Modalities in Myofascial Pain Syndrome

Led by Biruni University · Updated on 2026-02-17

60

Participants Needed

1

Research Sites

7 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to evaluate the effects of classical massage on pain, muscle sensitivity, muscle activity, functional status, and quality of life in individuals with myofascial pain syndrome, and to compare the effectiveness of classical massage applied alone versus in combination with a conventional physiotherapy program.

CONDITIONS

Official Title

Comparison of Treatment Modalities in Myofascial Pain Syndrome

Who Can Participate

Age: 30Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of myofascial pain syndrome confirmed by a physician according to Travell and Simons criteria (1992)
  • Male or female aged 30 to 50 years
  • At least one active trigger point in the upper trapezius muscle confirmed by palpation
  • Pain radiating to the neck and upper extremity lasting at least 3 months
  • Pain intensity of 4 or higher on the Visual Analog Scale (VAS)
  • Functional impairment shown by a Neck Disability Index (NDI) score of 10 or more out of 50 (20% or higher)
  • Written informed consent provided
Not Eligible

You will not qualify if you...

  • Diagnosed systemic musculoskeletal or rheumatologic disorders such as fibromyalgia or rheumatoid arthritis
  • Signs or symptoms of neuropathic pain or cervical radiculopathy
  • Conditions that prevent massage therapy like skin infection, open wounds, bleeding disorders, or active inflammation
  • Receipt of manual therapy, massage, dry needling, injections, or similar treatments targeting the affected area within the last month
  • Pregnancy or breastfeeding
  • History of acute trauma, fracture, or surgery involving the neck or shoulder region

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Biruni University

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

B

Begüm Kara Kaya, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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