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RecruitingNCT06668649Updated Nov 8, 2024

Polish Version Fatigue Severity Scale

An observational study in Multiple Sclerosis, Amyotrophic Lateral Sclerosis and Stroke, Ischemic, sponsored by Jakub Antczak. Recruiting at 2 sites in Poland. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-11-08.

Sponsored by Jakub Antczak · Observational

From the registry’s dates

  • Started Nov 2024; still recruiting 1 year 11 months later.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
310
Ages
18 Years and older
Sex
All
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Study summary

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.

Read the detailed description

Fatigue is one of main symptoms in multiple sclerosis, amyotrophic lateral sclerosis, post-polio syndrome, stroke, parkinsonism as well as in the chronic fatigue syndrome. It has profound effect on quality of life and professional and social functioning and in multiple sclerosis it is described as the worst symptoms by the 50% of patients. It is defined as the difficulty in initiating and maintaining a sustained mental or physical activity. Not infrequent it is misdiagnosed as sleepiness or other symptom. Fatigue severity scale (FSS) is a time efficient and easy to apply instrument to assess the impact of fatigue on patient's life. It has been translated and validated in Turkish, Russian, Hindi, Portuguese, and many other languages. FSS is a short, nine-item self-report questionnaire. Each item is a Likert scale, scored from one to seven, where seven refers to the most severely expressed aspect of fatigue. The aim of this study is to validate the Polish-language version of the Fatigue Severity Scale (pFSS). This version has been created according to widely accepted, respective standards, including translation by two independent native Polish-language speakers with acquired knowledge of English and backward translation by two independent native English-language speakers with acquired knowledge of Polish as well as with the pretesting on ten patients.

02

Conditions studied

  • Multiple Sclerosis
  • Amyotrophic Lateral Sclerosis
  • Stroke, Ischemic

Keywords

  • Fatigue
  • Multiple Sclerosis
  • stroke
  • quality of life
03

In context

Multiple Sclerosis

3,460 studies on the registry are indexed under Multiple Sclerosis; 661 are open to participants now.

This study's planned enrollment of 310 is above the median of 100 across 1,016 observational studies indexed under Multiple Sclerosis.

Browse Multiple Sclerosis studies →

Lead sponsor

Jakub Antczak is the lead sponsor of 8 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants will be recruited from the neurologic ambulatories and neurologic clinics of Jagiellonian University Medical College in Cracow and of Institute of Psychiatry and Neurology in Warsaw. Healthy controls will be recruited from personel of those facitlites as well as from the relatives of members of research team.

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • Presence of cognitive deficits or behavioral disorder, which could disturb participation in the study.
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
310 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patients

    Both sexes, aged 18 or older. The group will include 80 patients with multiple sclerosis, 80 patients with amyotrophic lateral sclerosis and 50 survivors of ischemic stroke

    Diagnostic Test: Testing with Questionnaires

  • Control

    Both sexes, aged 18 or older. The group will include 100 healthy controls.

    Diagnostic Test: Testing with Questionnaires

Interventions

  • Diagnostic testTesting with Questionnaires

    Testing with following Questionnaires: pFSS, Polish-language version of Modified Fatigue Impact Scale, Visual Analogue Scale of Fatigue, EQ-5D-5L (EuroQol-5 dimension) questionnaire, Beck Depression Inventory II. In randomly selected 30 patients and 20 controls questionnaires will be administered twice with two weeks interval to assess the test-retest reliability.

06

What researchers measure

Primary outcomes

  1. Internal Consistency

    Consistency between particular items of Polish language version of the Fatigue Severity Scale will be evaluated using Cronbach alfa test. The score of the Polish language version of the Fatigue Severity Scale ranges between 9 and 63 with higher scores meaning a worse outcome.

    Time frame: Through study completion, an average of 1 year

  2. Validity

    Validity will be tested by calculating the correlation of Polish language version of the Fatigue Severity Scale score with scores of Polish-language version of Modified Fatigue Impact Scale. The score of the Polish language version of the Fatigue Severity Scale ranges between 9 and 63 with higher scores meaning a worse outcome. The score of the Modified Fatigue Impact Scale ranges between 0 and 84 with higher scores meaning a worse outcome.

    Time frame: Through study completion, an average of 1 year

  3. Reliability

    Reliability will be tested by calculating the correlation between Polish language version of the Fatigue Severity Scale scores from the 1st and 2nd administration in the randomly selected subgroup of patients and controls. The score of the Polish language version of the Fatigue Severity Scale ranges between 9 and 63 with higher scores meaning a worse outcome.

    Time frame: Through study completion, an average of 1 year

Secondary outcomes

  1. Impact of fatigue on quality of life - index

    Correlation between Polish language version of the Fatigue Severity Scale score and the index score of EQ-5D-5L (EuroQol-5 dimension) questionnaire. The score of the Polish language version of the Fatigue Severity Scale ranges between 9 and 63 with higher scores meaning a worse outcome. The index score of EQ-5D-5L (EuroQol-5 dimension) questionnaire ranges between -0.59 to 1 with higher scores indicating better outcome.

    Time frame: Through study completion, an average of 1 year

  2. Impact of fatigue on quality of life - visual analogue scale

    Correlation between Polish language version of the Fatigue Severity Scale score and the visual analogue scale score of EQ-5D-5L (EuroQol-5 dimension) questionnaire. The score of the Polish language version of the Fatigue Severity Scale ranges between 9 and 63 with higher scores meaning a worse outcome. The visual analogue scale score of EQ-5D-5L (EuroQol-5 dimension) questionnaire ranges between 0 to 100 with higher scores indicating better outcome.

    Time frame: Through study completion, an average of 1 year

  3. Impact of fatigue on depression

    Correlation between Polish language version of the Fatigue Severity Scale score and score of Beck Depression Inventory II. The score of the Polish language version of the Fatigue Severity Scale ranges between 9 and 63 with higher scores meaning a worse outcome. The score of the Beck Depression Inventory II ranges between 0 and 63 with higher scores indicating worse outcome.

    Time frame: Through study completion, an average of 1 year

  4. Difference in fatigue level between patients and controls

    Difference in Polish language version of the Fatigue Severity Scale score between patients and controls. The score of the Polish language version of the Fatigue Severity Scale ranges between 9 and 63 with higher scores meaning a worse outcome.

    Time frame: Through study completion, an average of 1 year

07

Study locations

2 of 2 sites recruiting
  • Jagiellonian University Medical College, Department of Neurology
    Kraków, Lesser Poland 31503, Poland
    • Jakub M Antczak, MD · Contact · jakub.antczak@uj.edu.pl · +48 795 421 153
    • Gabriela Rusin, MD · Contact · gabriela.rusin@doctoral.uj.edu.pl · +48 601 661 607
    • Magdalena Spaczyńska-Boczar, MD · Sub investigator
    • Marcin Wnuk, MD · Sub investigator
    • Gabriela G Rusin, MD · Sub investigator
    Recruiting
  • Institute of Psychiatry and Neurology
    Warsaw, 02957, Poland
    Recruiting
08

References and documents

Publications

  • Guillemin F, Bombardier C, Beaton D. Cross-cultural adaptation of health-related quality of life measures: literature review and proposed guidelines. J Clin Epidemiol. 1993 Dec;46(12):1417-32. doi: 10.1016/0895-4356(93)90142-n. PubMed 8263569 ↗

Individual participant data

Plan to share: Yes — After the study is completed, the scans of collected questionnaires will be available upon request sent to the e-mail: jakub.antczak@uj.edu.pl

Supporting information: Study protocol

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 8, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06668649
Lead sponsor
Jakub Antczak
Collaborators
Institute of Psychiatry and Neurology, Warsaw
Responsible party
Jakub Antczak (Principal Investigator, Jagiellonian University) — Sponsor-investigator
First posted
Oct 31, 2024
Start date
Nov 4, 2024
Primary completion
Dec 31, 2026 (estimated)
Completion
Mar 31, 2027 (estimated)
Last update
Nov 8, 2024

Study contacts

Jakub M Antczak, MD
Contact
jakub.antczak@uj.edu.pl
+48 12 400 25 50
Gabriela G Rusin, MD
Contact
gabriela.rusin@alumni.uj.edu.pl
+48 12 400 25 50
Jakub M Antczak, MD
principal investigator · Jagiellonian University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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