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FIMS

Fatigue in MS: from invisible to measurable - FIMS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON58014
Enrollment
40
Registered
2025-02-21
Start date
2025-10-27
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Diagnosis of MS Age 18-60 Ability to perform the foot-tapping task Ability to walk at least 20 meters (with or without walking aid)

Exclusion criteria

Exclusion criteria: - Medication use with dimethyl fumarate, fingolimod or alemtuzumab - MS relapse 6 weeks before the start of the study - Change in medication within 6 weeks of the start of the study - Having a psychiatric disorder - Having a neurological disorder other than MS - Having cognitive or communicative problems that makes it hard to follow instructions - Had an infection in the last month - Received a vaccination in the last 14 days - Pregnant or pregnancy in the last 6 months

Design outcomes

Primary

MeasureTime frame
Scores from the fatigue questionnaires and decline in amplitude and frequency from the performance fatiguability test will be correlated to the level of CD4 CTLs from the blood samples. 

Secondary

MeasureTime frame
Muscle activation patterns measured by EMG, distance walked on 6MWT and voluntary muscle activation.

Countries

Netherlands

Contacts

Public ContactN Dreijer

Universitair Medisch Centrum Groningen

n.dreijer@umcg.nl0625647172

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: May 1, 2026