Multiple Sclerosis (MS) Clinical Trials

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Non-invasive Brain Stimulation for Altering Neuro-inflammatory Mediators of Central Fatigue in Multiple Sclerosis

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

The neurobiological basis of central fatigue in multiple sclerosis remained unclear so far. This study investigates reward-related brain mechanisms, inflammation, and their modulation by non-invasive brain stimulation using fMRI, proteomics, and clinical measures to improve future treatment of central fatigue in MS. In the study, persons suffering from relapsing-remitting MS (RRMS) with vs. without comorbid central fatigue will be included. The study comprises five experimental visits conducted at Charité University Medicine on five consecutive days (i.e., V1 - V5) and two follow-up visits two (V6) and four (V7) weeks after V5. True or sham anodal transcranial Direct Current Stimulation (tDCS) is applied to the left dorsolateral prefrontal cortex (dlPFC) at the five visits V1 to V5. All primary and secondary outcomes are assessed at V1 and V5. At V6 and V7, measures of central fatigue are additionally assessed via questionnaires which are send to and back from the patients via mail. Participants of all groups will participate in all visits.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Men and women

‣ 18 - 70 years

⁃ Established MS diagnosis (relapsing-remitting MS; RRMS) prior to study inclusion

⁃ Maximal EDSS of 4

⁃ Maximal disease duration 10 years

⁃ Existing health insurance

⁃ Stable or no treatment with disease modifying treatment (DMT) in last six months prior to study onset

⁃ Persons with RRMS and FSMC score ≥ 22 will be included in group RRMS with fatigue

⁃ Persons with RRMS and FSMC score \< 22 will be included in group RRMS without fatigue

Locations
Other Locations
Germany
Charité Campus Mitte
RECRUITING
Berlin
Contact Information
Primary
Janina Dr. Behrens, Dr. med.
janina.behrens@charite.de
+49 30 7560921
Backup
Martin Dr. Weygandt, PhD
martin.weygandt@mdc-berlin.de
Time Frame
Start Date: 2026-03-02
Estimated Completion Date: 2028-06
Participants
Target number of participants: 84
Treatments
Active_comparator: tDCS Stimulation of dlPFC
Medical device: tDCS Stimulation over left dorsolateral prefrontal cortex (DLPFC) for 20 min daily over 5 consecutive days
Sham_comparator: Sham Stimulation of dlPFC
Medical device: Placebo Sham stimulation over left dorsolateral prefrontal cortex (dlPFC) for 20 min daily over 5 consecutive days
Related Therapeutic Areas
Sponsors
Leads: Charite University, Berlin, Germany

This content was sourced from clinicaltrials.gov