Wiley, Internal Medicine Journal, 6(51), p. 988-992, 2021
DOI: 10.1111/imj.15357
Full text: Unavailable
AbstractClinical quality registries are increasingly utilised to monitor and improve healthcare quality. Opt‐out consent is recommended to maximise participation and ensure validity of data, however, presents specific considerations when including persons with impaired decision‐making abilities. This paper describes the innovative Australian Dementia Network Registry recruitment framework designed to optimise inclusion of people with dementia and mild cognitive impairment.