2019
DOI: 10.2196/12327
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Requirements for an Electronic Health Tool to Support the Process of Help Seeking by Caregivers of Functionally Impaired Older Adults: Co-Design Approach

Abstract: Background In Quebec, Canada, many public, community, and private organizations provide resources to caregivers of functionally impaired older adults. Nevertheless, these resources may be difficult for caregivers to find. A co-design study was conducted to address the gap between caregivers and access to resources. The purpose of this study was to support the process of help seeking by caregivers of functionally impaired older adults through electronic health (eHealth). Objective … Show more

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Cited by 17 publications
(9 citation statements)
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“…Moreover, if decisions regarding content, functionality, and design are guided by real-life experiences of prospective users, this helps to ensure the appropriateness and relevance of self-management applications. Involving prospective users also fosters trust and the credibility of the technology, thus increasing the likelihood of system acceptance and, as a result, accelerating adoption into practice [ 20 , 21 ].…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, if decisions regarding content, functionality, and design are guided by real-life experiences of prospective users, this helps to ensure the appropriateness and relevance of self-management applications. Involving prospective users also fosters trust and the credibility of the technology, thus increasing the likelihood of system acceptance and, as a result, accelerating adoption into practice [ 20 , 21 ].…”
Section: Introductionmentioning
confidence: 99%
“…Following the identification of needs, CoDs 3, 4, 5, and 6, along with the second AC, allowed for identification of the requirements (functionalities and content) that must be included to meet the needs. Tremblay et al [23] describe this part of the project. Please also note that content elements were developed throughout the 8 CoDs.…”
Section: Resultsmentioning
confidence: 99%
“…Patients should be able to delineate the level of involvement of their caregiver if they are able; a process that dovetails with existing approaches to health care proxy designation but adds further instruction for caregiver involvement. Additionally, health systems could design space in the electronic medical record for documenting decisions made with caregiver input or even flag support resources targeted to caregivers (Loeslie et al, 2017; Tremblay et al, 2019). Another approach is patient/caregiver-oriented discharge summaries as we know care transitions, especially facility to home, are points at which errors in communication can occur (Hahn-Goldberg et al, 2016).…”
Section: Discussionmentioning
confidence: 99%