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Fatigue in Sjögren's Syndrome: a Randomized Controlled Trial of Combined Non-pharmacological Therapeutic Strategies

Status: Recruiting
Location: See location...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Unexplained fatigue is a frequent (60-70%) chronic complaint in Sjögren's syndrome (SjS) with a clear unmet therapeutic need, despite the recommendation of adapted physical activity (APA) programs, which are effective and feasible, but only to some extent. Hence, other therapeutic approaches, such as Acupuncture (ACU) or transcutaneous vagal nerve stimulation (tVNS), have been evaluated during the past years, with varying degrees of success in alleviating fatigue. FESSONA has been designed as a randomized controlled monocentric trial, aiming at comparing the effects of 3 different programs on fatigue in SjS: APA alone, APA+ACU and APA+tVNS. Relevant controls will be included as well (sham ACU and simulated tVNS). Multiple fatigue and SjS-related features will be measured before (at inclusion) and after (week 12) the intervention, as well as at week 24 and 48, to evaluate the short- and long-term impact of each program. Tolerance and feasibility will also be evaluated.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient affiliated or entitled to a social security scheme.

• Age \> 18 years.

• Patient informed and having signed the information form and consent to participate in the study.

• Patient with Sjögren's syndrome according to ACR/EULAR 2016 or AECG 2002 criteria, usually followed up every year or more frequently

• Fatigue present for ≥ 6 months, without obvious explanation and/or specific treatment to conduct (e.g., disease's flare, chronic infection), with a current FACIT-F score \< 34

Locations
Other Locations
France
Chu de Saint-Etienne
RECRUITING
Saint-etienne
Contact Information
Primary
Martin KILLIAN, MD
martin.killian@chu-st-etienne.fr
(33)477 82 91 79
Backup
Florence RANCON, Chef de projet
florence.rancon@chu-st-etienne.fr
(33)477829458
Time Frame
Start Date: 2026-03-24
Estimated Completion Date: 2028-04
Participants
Target number of participants: 174
Treatments
Experimental: APA + sham ACU + tVNS
Experimental: APA + ACU + simulated tVNS
Sham_comparator: APA + Simulated tVNS + sham ACU
Sponsors
Leads: Centre Hospitalier Universitaire de Saint Etienne

This content was sourced from clinicaltrials.gov