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Recruiting Not applicable

Physiotherapy Methods for Fibromyalgia

NCT07425652 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-01
Last updated
2026-06-16

Condition(s) studied

Fibromyalgia

Investigational drug(s) / intervention(s)

Connective tissue massageTranscutaneous auricular vagus nerve stimulation

Connective tissue massage: Connective tissue massage (CTM) is a manual technique that involves applying specific dragging or pulling movements to the superficial and subcutaneous connective tissue layers

Transcutaneous auricular vagus nerve stimulation: Transcutaneous auricular vagus nerve stimulation (taVNS) is a non-invasive neuromodulation technique. It targets vagus nerve stimulation through the transcutaneous application of electrical impulses to the auricle

Study summary

The aim of our study was to examine and compare the effects of different physiotherapy methods, namely connective tissue massage, transcutaneous auricular vagus nerve stimulation and both, on pain, health status, sleep quality, fatigue, psychosocial status, autonomic symptoms and quality of life in women with fibromyalgia.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Having been diagnosed with fibromyalgia * Being female between the ages of 18-65 * Volunteering to participate in the study Exclusion Criteria: * Diagnosed neurological and infectious diseases * Uncontrolled endocrine and/or autoimmune diseases * Serious psychiatric disorders (bipolar disorder, schizophrenia, psychosis, etc.) * Pregnancy or breastfeeding * Malignancy * History of known arrhythmia or any implanted electronic device * Presence of sensory loss * Acute inflammation, open wounds, erythema in massage areas * History of any surgery within the last 6 months * Having received physical therapy for FM within the last 6 months and/or being included in a new treatment program during the study period

Primary outcome measure(s)

  • Pain intensity as measured by the Visual Analog Scale (VAS) — Baseline, 6th week (after treatment)
    In the VAS scale, which is a 10 cm scale, '0' represents no pain and '10' represents the worst imaginable pain. The distance from the marked point to the 0 point is measured using a ruler, and the pain intensity is recorded in centimeters.
  • Health status and disease severity as measured by the Fibromyalgia Impact Questionnaire (FIQ). — Baseline, 6th week (after treatment)
    This questionnaire assesses the severity of symptoms, overall impact, and physical function. The total score for the questionnaire ranges from 0 to 100, with higher scores indicating a greater impact of the illness on patients.

Trial sites (1)

FacilityCityRegionStatus
Gazi Mustafa Kemal Occupational and Environmental Diseases Hospital Ankara Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07425652 on ClinicalTrials.gov ↗ ← All trials in Turkey