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	Frågeformulär för kronisk hjärtsvikt	Parkinson's Disease Questionnaire-39
Ämnesområde	Hälsoutfall	Hälsoutfall
Familj	Process / pipeline	Process / pipeline
Ursprungsår	2000	1997
Upphovsperson	Luc Guyonnet et al.	Crispin Jenkinson et al.
Typ	Self-report quality of life questionnaire	Self-report quality of life questionnaire
Ursprungskälla	Guyonnet, S., Vellas, B., Garry, P. J., & Albarede, J. L. (2000). The Chronic Heart Failure Questionnaire: A pilot study of validity, reliability, and responsiveness. Journal of Cardiac Failure, 6(1), 21-26.	Jenkinson, C., Fitzpatrick, R., Peto, V., Greenhall, R., & Hyman, N. (1997). The Parkinson's Disease Questionnaire (PDQ-39): Development and validation of a Parkinson's disease summary index score. Age and Ageing, 26(5), 353-357.
Alias	CHQ, Heart Failure Quality of Life, Chronic Heart Failure QoL	PDQ-39, Parkinson's Disease Questionnaire, PDQ
Närliggande	4	4
Sammanfattning	The CHQ is a disease-specific quality of life measure for chronic heart failure (CHF). Developed by Luc Guyonnet and colleagues in 2000, this 20-item questionnaire assesses how heart failure affects dyspnea, fatigue, emotional function, and activity limitation. It is used in heart failure clinical trials and research to quantify patient-experienced burden and treatment benefit.	The PDQ-39 is the most widely used patient-reported outcome measure for Parkinson's disease quality of life. Developed by Crispin Jenkinson and colleagues in 1997, this 39-item self-report questionnaire comprehensively assesses how Parkinson's symptoms affect daily functioning, emotional well-being, stigma, social support, and cognitive-communication abilities. It is the recommended instrument in major Parkinson's disease clinical trials and forms a core component of outcome measurement in movement disorders.