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Completed

NCT Number: NCT07577102

Unilateral and Bilateral taVNS in Fibromyalgia

This randomized controlled trial aimed to compare the effects of unilateral (left-sided) and bilateral transcutaneous auricular vagus nerve stimulation (taVNS) combined with a home exercise program on clinical outcomes, autonomic nervous system function, and exercise performance in individuals with fibromyalgia syndrome (FMS).

Participants diagnosed with fibromyalgia were randomly assigned to one of three groups: unilateral taVNS, bilateral taVNS, or a home exercise program. The intervention period lasted two weeks and included ten treatment sessions. Clinical outcomes were assessed using validated scales including the Fibromyalgia Impact Questionnaire (FIQ), Beck Anxiety Inventory (BAI), Beck Depression Inventory (BDI), and Pittsburgh Sleep Quality Index (PSQI). Autonomic function was evaluated using heart rate variability (HRV) parameters, and exercise performance was assessed based on repetition capacity.

The study aimed to determine whether bilateral stimulation provides additional benefits compared to unilateral stimulation and exercise alone. The findings may contribute to understanding the role of neuromodulation strategies in improving autonomic regulation, symptom severity, and functional performance in individuals with fibromyalgia.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Darülaceze Medical Center

Istanbul, Turkey (Türkiye)

About this study

Fibromyalgia syndrome (FMS) is a chronic condition characterized by widespread pain, fatigue, sleep disturbances, and psychological symptoms, often associated with autonomic nervous system dysfunction. Reduced heart rate variability (HRV) and increased sympathetic activity are commonly observed in individuals with FMS, contributing to impaired exercise tolerance and reduced quality of life.

Transcutaneous auricular vagus nerve stimulation (taVNS) is a non-invasive neuromodulation technique that targets the auricular branch of the vagus nerve and has been shown to influence autonomic regulation and central pain processing. However, evidence regarding its effects on exercise performance and the comparative efficacy of unilateral versus bilateral stimulation remains limited.

This study was designed as a randomized controlled trial including individuals diagnosed with fibromyalgia. Participants were allocated into three groups: unilateral taVNS, bilateral taVNS, and a home exercise program. The interventions were applied over a two-week period consisting of ten sessions. The taVNS intervention was administered via auricular stimulation targeting vagal afferents, while the exercise group followed a structured home-based program.

Outcome measures included clinical symptom scales (FIQ, BAI, BDI, PSQI), autonomic nervous system parameters derived from HRV analysis (including RMSSD, pNN50, LF, HF, and LF/HF ratio), and exercise performance assessed through repetition capacity. Assessments were conducted before and after the intervention period.

The primary objective was to compare the effects of unilateral and bilateral taVNS on autonomic function and exercise performance, and to evaluate whether combining neuromodulation with exercise provides additional clinical benefits in individuals with fibromyalgia. The results of this study may help inform rehabilitation strategies integrating neuromodulation and exercise-based interventions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Were between 18 and 45 years of age
  • Were diagnosed with fibromyalgia according to the 2016 ACR diagnostic criteria

-- Stable clinical condition

  • Ability to understand and follow study procedures
  • Willingness to participate and provide informed consent

Exclusion criteria

  • A history of malignancy
  • Cardiopulmonary diseases contraindicating exercise
  • Limb loss
  • Ear infections and implants, implanted electronic devices
  • Systemic diseases (hematological, endocrine, rheumatological, renal, cardiovascular, gastrointestinal, neurological, or autoimmune diseases)
  • Active infection
  • Surgery or major trauma within the previous 6 months
  • Postmenopausal status
  • Pregnancy or lactation

Treatment and study plan

taVNS

Device

Transcutaneous auricular vagus nerve stimulation applied via the auricular branch of the vagus nerve for neuromodulation purposes.

Home Exercise Program

Behavioral

A structured home-based exercise program including strengthening and mobility exercises performed over a two-week period.

Primary outcomes

  1. Exercise performance (repetition count)

    Time frame: Baseline (Week 0) and Week 2

    Number of repetitions performed during exercise sessions to evaluate functional exercise performance.

Secondary outcomes

  1. Fibromyalgia Impact Questionnaire (FIQ) score

    Time frame: Baseline (Week 0) and Week 2

    Change in Fibromyalgia Impact Questionnaire (FIQ) score (range: 0-100; higher scores indicate worse disease severity and functional impairment) to assess disease severity and functional status in patients with fibromyalgia.

  2. Beck Anxiety Inventory (BAI) score

    Time frame: Baseline (Week 0) and Week 2

    Change in Beck Anxiety Inventory (BAI) score (range: 0-63; higher scores indicate greater anxiety levels) to assess anxiety severity.

  3. Beck Depression Inventory (BDI) score

    Time frame: Baseline (Week 0) and Week 2

    Change in Beck Depression Inventory (BDI) score (range: 0-63; higher scores indicate more severe depressive symptoms) to assess depression severity.

  4. Pittsburgh Sleep Quality Index (PSQI) score

    Time frame: Baseline (Week 0) and Week 2

    Change in Pittsburgh Sleep Quality Index (PSQI) score (range: 0-21; higher scores indicate worse sleep quality) to assess sleep quality.

  5. Heart Rate Variability (RMSSD)

    Time frame: Week 0 pre-exercise measurement, Week 0 post-exercise measurement, Week 2 pre-exercise measurement, and Week 2 post-exercise measurement

    Change in RMSSD (ms), reflecting parasympathetic activity.

  6. Heart Rate Variability (pNN50)

    Time frame: Week 0 pre-exercise measurement, Week 0 post-exercise measurement, Week 2 pre-exercise measurement, and Week 2 post-exercise measurement

    Change in pNN50 (%), representing parasympathetic modulation.

  7. Heart Rate Variability (HF power)

    Time frame: Week 0 pre-exercise measurement, Week 0 post-exercise measurement, Week 2 pre-exercise measurement, and Week 2 post-exercise measurement

    Change in high-frequency (HF) power (ms²), reflecting parasympathetic nervous system activity.

  8. Heart Rate Variability (LF power)

    Time frame: Week 0 pre-exercise measurement, Week 0 post-exercise measurement, Week 2 pre-exercise measurement, and Week 2 post-exercise measurement

    Change in low-frequency (LF) power (ms²), reflecting mixed sympathetic and parasympathetic activity.

  9. Heart Rate Variability (LF/HF ratio)

    Time frame: Week 0 pre-exercise measurement, Week 0 post-exercise measurement, Week 2 pre-exercise measurement, and Week 2 post-exercise measurement

    Change in LF/HF ratio (unitless), indicating autonomic balance between sympathetic and parasympathetic systems.

Sponsors and collaborators

Lead sponsor

Istanbul Gelisim University

Other

Collaborators

  • Bahçeşehir University

Registry information

Official study title

Comparison of Unilateral and Bilateral Transcutaneous Auricular Vagus Nerve Stimulation on Autonomic Function and Exercise Performance in Fibromyalgia

Acronym: taVNS-FMS

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
May 11, 2026
Registry last updated
May 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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