Transcutaneous Vagus Nerve Stimulation as a Complementary Therapy to Exercise in Chronic Fatigue

NCT ID
NCT06170645
Registry status
Recruiting
Study type
Not specified in the registry data
Phase
Not applicable
Sponsor
Centre Hospitalier Universitaire de Saint Etienne

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 60 participants (Estimated).

What is being studied

No interventions are listed in the registry data.

Who may be eligible

Ages
Not specified in the registry data
Sex
Not specified in the registry data
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Patient over 18 years old * Signature of informed consent * Confirmed diagnosis of fibromyalgia or long Covid (ACR 2016 criteria and persistent symptoms lasting more than 6 months after a positive RT-PCR test, respectively) * Persistent fatigue after an exercise rehabilitation program (FSS score \> 36) * Physical inactivity, i.e. \<150 minutes per week of physical activity Exclusion Criteria: * Pre-existing atrial fibrillation, * Left ventricular ejection fraction \<40% * Severe heart failure * Recent stroke or myocardial infarction (\<6 months) * Unilateral or bilateral vagotomy * Pregnancy or breastfeeding

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: France

Sample of listed locations

  • Centre Hospitalier de Saint-Etienne — Saint-Etienne, 42055, France — Site recruitment status not specified in the registry data

Study details

Start date
October 3, 2024
Primary completion date
February 1, 2028
First posted
December 14, 2023

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT06170645
Registry last updated
May 6, 2026
QualifiedStudies registry data refreshed
September 21, 2026

View NCT06170645 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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