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Huntington's Disease Health-Related Quality of Life Scale (HD-QoL)×Stroke-Specifik Livskvalitetsskala (SS-QoL)×
FagområdeNeurologiNeurologi
FamilieProcess / pipelineProcess / pipeline
Oprindelsesår20011999
OphavspersonHelder et al., University of LeidenLee S. Williams, Indiana University
TypeSelf-report questionnaireSelf-report questionnaire
Oprindelig kildeHelder, D. I., Kaptein, A. A., van Kempen, G. M., Weinman, J., van Houwelingen, H. C., & Roos, R. A. (2001). Living with Huntington's disease: Illness perceptions, coping mechanisms, and patients' well-being. Journal of Psychosomatic Research, 50(1), 1-7. DOI ↗Williams, L. S., Weinberger, M., Harris, L. E., Clark, D. O., & Biller, J. (1999). Development of a Stroke-Specific Quality of Life Scale. Stroke, 30(7), 1362-1369. DOI ↗
AliasserHuntington Disease QoL, HD-QoL ScaleStroke-Specific QoL, SS-QOL
Relaterede44
ResuméThe HD-QoL is a disease-specific quality-of-life instrument designed to measure the multidimensional impact of Huntington's disease on patients' physical, emotional, social, and cognitive functioning. Developed by Helder and colleagues in 2001, it uniquely addresses the progressive motor, cognitive, and psychiatric manifestations characteristic of HD. The scale recognizes that HD burden extends beyond neurological deficits to profound impacts on identity, family relationships, and existential well-being.The SS-QoL is a disease-specific quality-of-life instrument designed to capture the multidimensional impact of stroke on survivors' functional and emotional well-being. Developed by Williams and colleagues in 1999, this 49-item scale addresses stroke-specific concerns including language, cognition, mobility, and emotional functioning. It is a gold-standard instrument for stroke outcome research and routine clinical monitoring of post-stroke recovery.
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ScholarGateSammenlign metoder: HD-QoL · SS-QoL. Hentet 2026-06-19 fra https://scholargate.app/da/compare