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	Caregiver Quality of Life Index–Cancer	McGill Quality of Life Questionnaire
Ämnesområde	Palliativ vård	Palliativ vård
Familj	Process / pipeline	Process / pipeline
Ursprungsår	1999	1995
Upphovsperson	Weitzner, Jacobsen, Wagner, and Friedland	Cohen, Mount, Strobel, and Bui
Typ	Self-report	Self-report
Ursprungskälla	Weitzner, M. A., Jacobsen, P. B., Wagner, H., & Friedland, J. L. (1999). The Caregiver Quality of Life Index–Cancer (CQOLC) scale: development and validation of an instrument to measure quality of life of the primary family caregiver of patients with cancer. Quality of Life Research, 8(1), 55–63.	Cohen, S. R., Mount, B. M., Strobel, M. G., & Bui, F. (1995). The McGill Quality of Life Questionnaire: a measure of quality of life appropriate for people facing advanced cancer. Journal of Palliative Care, 11(3), 6–15.
Alias	CQOLC, Caregiver QoL-Cancer	MQOL
Närliggande	5	5
Sammanfattning	The Caregiver Quality of Life Index–Cancer (CQOLC) is a 35-item self-report measure specifically designed to assess the quality of life and burden experienced by family members caring for cancer patients. Developed by Weitzner and colleagues in 1999, the CQOLC captures the multifaceted impact of caregiving—physical strain, emotional toll, disruption of daily activities, financial hardship, and positive adaptation—making it essential for identifying caregiver distress and tailoring support interventions.	The McGill Quality of Life Questionnaire (MQOL) is a 17-item, multidimensional self-report measure specifically developed for people with advanced cancer and other life-limiting illnesses. Created by Cohen, Mount, and colleagues at McGill University in 1995, the MQOL captures physical, functional, emotional, spiritual, and social dimensions of quality of life in a concise, patient-centered format. It has become a standard outcome measure in palliative care research, hospice quality improvement, and cancer centers internationally.