Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06668649

Polish Version Fatigue Severity Scale

Led by Jakub Antczak · Updated on 2024-11-08

310

Participants Needed

2

Research Sites

125 weeks

Total Duration

On this page

Sponsors

J

Jakub Antczak

Lead Sponsor

I

Institute of Psychiatry and Neurology, Warsaw

Collaborating Sponsor

AI-Summary

What this Trial Is About

Fatigue is one of main symptoms in multiple sclerosis, amyotrophic lateral sclerosis and other diseases with profound effect on quality of life and professional and social functioning. Not infrequent it is misdiagnosed as sleepiness or other symptom. Fatigue severity scale is a time efficient and easy to apply instrument to assess the impact of fatigue on patient's life. The aim of this study is to validate the Polish-language version of the Fatigue Severity Scale.

CONDITIONS

Official Title

Polish Version Fatigue Severity Scale

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of definite multiple sclerosis or definite, laboratory-supported multiple sclerosis, or definite amyotrophic lateral sclerosis, or probable amyotrophic lateral sclerosis or probable, laboratory supported amyotrophic lateral sclerosis or ischemic stroke or - for healthy controls - lack of diseases, pharmacotherapy or habits, which could induce abnormal tiredness
Not Eligible

You will not qualify if you...

  • Presence of cognitive deficits or behavioral disorder, which could disturb participation in the study.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Jagiellonian University Medical College, Department of Neurology

Krakow, Lesser Poland Voivodeship, Poland, 31503

Actively Recruiting

2

Institute of Psychiatry and Neurology

Warsaw, Poland, 02957

Actively Recruiting

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Research Team

J

Jakub M Antczak, MD

CONTACT

G

Gabriela G Rusin, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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