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Quality of Life

Impact of severe intellectual disability on proxy instrumental assessment of quality of life

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Zachary J. Hankle, Dane C. Bluestone, Jennifer K. Kramer, Palak Bassi & Anthony J. Goreczny. (2022) What activities individuals with intellectual disabilities do for fun: exploration into self-care. International Journal of Developmental Disabilities 68:5, pages 712-722.
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Tess Tournier, Alexander H. C. Hendriks, Andrew Jahoda, Richard P. Hastings, Sanne A. H. Giesbers & Petri J. C. M. Embregts. (2022) Perspectives of people with intellectual disability about their family networks: A comparison study with key support worker proxy reports. Journal of Intellectual & Developmental Disability 47:1, pages 27-38.
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Jan Šiška, Pavel Čáslava, Jiří Kohout, Julie Beadle-Brown, Zuzana Truhlářová & Markéta Kateřina Holečková. (2021) What matters while assessing quality of social services? Stakeholders’ perspective in Czechia. European Journal of Social Work 24:5, pages 864-883.
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Articles from other publishers (3)

Margherita Cameranesi, Katherine Chimney & Shahin Shooshtari. (2022) Changes in the quality of life of persons with profound intellectual and multiple disabilities following community transition: A Canadian study. Research in Developmental Disabilities 131, pages 104360.
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Johannes Fellinger, Magdalena Dall, Joachim Gerich, Maria Fellinger, Katharina Schossleitner, William Joseph Barbaresi & Daniel Holzinger. (2020) Is it feasible to assess self-reported quality of life in individuals who are deaf and have intellectual disabilities?. Social Psychiatry and Psychiatric Epidemiology 56:10, pages 1881-1890.
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Nellyn Lutur. (2020) PROMOTION AND QUALITY OF SERVICE WITH INTERESTS TO VISIT TOURIST OBJECTS: SISTEMATIC SEARCH. EUREKA: Social and Humanities 2, pages 3-7.
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