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The Functional Assessment of Chronic Illness Therapy–Fatigue (FACIT-Fatigue) scale in patients with...

The Functional Assessment of Chronic Illness Therapy–Fatigue (FACIT-Fatigue) scale in patients with...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e0f2a63199464245bdbc95a07620bddc

The Functional Assessment of Chronic Illness Therapy–Fatigue (FACIT-Fatigue) scale in patients with axial spondyloarthritis: psychometric properties and clinically meaningful thresholds for interpretation

About this item

Full title

The Functional Assessment of Chronic Illness Therapy–Fatigue (FACIT-Fatigue) scale in patients with axial spondyloarthritis: psychometric properties and clinically meaningful thresholds for interpretation

Publisher

Cham: Springer International Publishing

Journal title

Journal of Patient-Reported Outcomes, 2024-08, Vol.8 (1), p.92-15, Article 92

Language

English

Formats

Publication information

Publisher

Cham: Springer International Publishing

More information

Scope and Contents

Contents

Background
Fatigue is an important symptom for most patients with axial spondyloarthritis (axSpA). The FACIT-Fatigue is a 13-item patient-reported outcome (PRO) instrument that has been used in axSpA clinical trials to measure fatigue severity and impact on daily activities. However, the psychometric properties of the FACIT-Fatigue are not fully evaluated across the entire spectrum of axSpA including non-radiographic axSpA (nr-axSpA) and radiographic axSpA (r-axSpA). This study determined: (1) the psychometric properties of the FACIT-Fatigue in nr-axSpA, r-axSpA, and the broad axSpA population and (2) FACIT-Fatigue scores representing meaningful within-patient change (MWPC), meaningful between-group differences, and cross-sectional severity bands.
Methods
Data from two Phase 3 trials in adults with nr-axSpA (BE MOBILE 1;
N
 = 254) and r-axSpA (BE MOBILE 2;
N
 = 332) were analyzed pooled and separately to assess the psychometric properties of the FACIT-Fatigue. MWPC and meaningful between-group difference estimates were derived using anchor-based and distribution-based methods. Cross-sectional fatigue severity bands were estimated using logistic regression analysis.
Results
The FACIT-Fatigue presented good internal consistency, adequate convergent and known-groups validity, and was sensitive to change over time across the full axSpA spectrum. A 5–11-point increase in FACIT-Fatigue score was estimated to represent a MWPC, with an 8-point increase selected as the responder definition. A 2.14–5.34-point difference in FACIT-Fatigue score change over a 16-week period was estimated to represent a small-to-medium meaningful between-group difference. FACIT-Fatigue score severity bands were defined as: none or minimal (>40), mild (>30 to ≤40), moderate (>21 to ≤30), and severe (≤21).
Conclusions
These findings support the use of the FACIT-Fatigue as a fit-for-purpose measure to assess fatigue-related treatment benefit in axSpA clinical trials. The proposed score estimates and thresholds can guide FACIT-Fatigue score interpretation across the full axSpA spectrum.
Trial registration
ClinicalTrials.Gov, NCT03928704. Registered 26 April 2019—Retrospectively registered,
https://classic.clinicaltrials.gov/ct2/show/NCT03928704
. ClinicalTrials.Gov, NCT03928743. Registered 26 April 2019—Retrospectively registered,
https://classic.clinicaltrials.gov/ct2/show/NCT03928743
.
Plain English summary
Fatigue is common in patients with axial spondyloarthritis (axSpA)—a painful...

Alternative Titles

Full title

The Functional Assessment of Chronic Illness Therapy–Fatigue (FACIT-Fatigue) scale in patients with axial spondyloarthritis: psychometric properties and clinically meaningful thresholds for interpretation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_e0f2a63199464245bdbc95a07620bddc

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e0f2a63199464245bdbc95a07620bddc

Other Identifiers

ISSN

2509-8020

E-ISSN

2509-8020

DOI

10.1186/s41687-024-00769-x

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