Cure8 research brief
Fatigue is a frequent, impactful symptom in Crohn’s disease that often goes unmeasured in clinic visits. Knowing which assessment tools exist can help patients and clinicians recognize and address fatigue.
Adults with Crohn’s disease, their caregivers, clinicians managing IBD, and researchers studying symptom measurement and quality of life.
This article is a scoping review that searched multiple databases and included 11 studies on tools used to clinically assess fatigue in people with Crohn’s disease.
The review reports that fatigue is multifactorial — linked to disease activity, immune factors, psychological and emotional issues, and sleep disturbance — and that validated instruments exist but are rarely used in routine practice.
The review cites prevalence estimates (about 47% during remission and 72% during active disease) reported in the included studies; these figures summarize what the source articles reported and are not independently verified here.
The practical takeaway is that fatigue significantly affects quality of life for people with Crohn’s disease, and greater routine assessment using validated tools may be warranted.
This record is a scoping review (abstract-level content provided). Prevalence figures and conclusions are drawn from the included studies; the review notes heterogeneity across studies and that fatigue assessment is uncommon in routine care.
Review the original publication for the complete reporting, methods, and context.
This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.
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