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	Fibromyalgipåverkansformulär	EORTC QLQ-C30
Ämnesområde	Hälsoutfall	Hälsoutfall
Familj	Process / pipeline	Process / pipeline
Ursprungsår	1991	1993
Upphovsperson	Cynthia S. Burckhardt et al.	Nico Aaronson et al.
Typ	Self-report symptom and functional impairment questionnaire	Self-report quality of life questionnaire
Ursprungskälla	Burckhardt, C. S., Clark, S. R., & Bennett, R. M. (1991). The Fibromyalgia Impact Questionnaire: Development and validation. The Journal of Rheumatic Diseases, 18(5), 728-735.	Aaronson, N. K., Ahmedzai, S., Bergman, B., Bullinger, M., Cull, A., Duez, N. J., ... & Takeda, F. (1993). The European Organisation for Research and Treatment of Cancer QLQ-C30: A quality-of-life instrument for use in international clinical trials in oncology. Journal of the National Cancer Institute, 85(5), 365-376.
Alias	FIQ, Fibromyalgia Impact, Fibromyalgia Questionnaire	QLQ-C30, EORTC QLQ-C30, Cancer Quality of Life Scale
Närliggande	4	5
Sammanfattning	The FIQ is the most widely used patient-reported outcome measure for fibromyalgia disease burden. Developed by Cynthia Burckhardt and colleagues in 1991, this 10-item questionnaire quantifies how fibromyalgia affects physical function, work capacity, depression, anxiety, sleep, pain, and fatigue. The revised version (FIQR, 21 items) offers enhanced psychometric properties and is the current standard in fibromyalgia clinical trials and practice.	The EORTC QLQ-C30 is the most widely used international instrument for assessing quality of life in cancer patients. Developed by the European Organisation for Research and Treatment of Cancer in 1993, it measures physical, emotional, cognitive, and social functioning alongside cancer-specific symptoms and financial impact, making it the standard outcome measure in oncology clinical trials and patient care.