A focus group study on the design considerations and impressions of a socially assistive robot for long-term care

Author(s):  
Wing-Yue Geoffrey Louie ◽  
Jacob Li ◽  
Tiago Vaquero ◽  
Goldie Nejat
2018 ◽  
Vol 30 (6) ◽  
pp. 634 ◽  
Author(s):  
Chi-Young Lee ◽  
Min-Hye Lee ◽  
Seong-Hyeon Lee ◽  
Yeon-Hwan Park

2020 ◽  
Author(s):  
Mohamed Amine Choukou ◽  
Sophia Mbabaali ◽  
Ryan East

BACKGROUND The number of Canadians with dementia is expected to rise to nearly 1 million individuals in the next decade. It is more than urgent to find a solution to monitor any unsafe behaviour that could be harmful to patients with dementia and the people around them such as other patients, professionals, or visitors. Current practice does not utilize systems to monitor behaviours of the patients with dementia (PwD) and send alerts when potential dangerous events occur. Events are reported randomly by non-professionals or when a professional notices an absence to a scheduled event. OBJECTIVE The purpose of this paper is to evaluate the potential of implementing a detector of behavioural disturbances (DBD) in long-term care homes through a mapping of the perceptions of clinicians and staff members towards this technology. METHODS A focus group was conducted with 8 clinicians and staff members and 1 partner of a PwD. RESULTS Three themes emerged from a thematic analysis of the perspectives of the stakeholders: (A) capability of the DBD to detect relevant dementia-related behavioural disturbances, (B) characteristics of the DBD and clinical needs and (C) DBD modalities of use. CONCLUSIONS The results confirmed the adequacy of the DBD for their daily needs in terms of detecting hazardous behaviours or personal and interpersonal behavioural disturbances. The DBD has been considered useful and easy to use by the focus group participants, meaning that the DBD has a high level of usability. CLINICALTRIAL NA


2020 ◽  
Vol 19 (1) ◽  
Author(s):  
Tamara Sussman ◽  
Sharon Kaasalainen ◽  
Rennie Bimman ◽  
Harveer Punia ◽  
Nathaniel Edsell ◽  
...  

Abstract Objectives Despite known benefits, advance care planning (ACP) is rarely a component of usual practice in long-term care (LTC). A series of tools and workbooks have been developed to support ACP uptake amongst the generable population. Yet, their potential for improving ACP uptake in LTC has yet to be examined. This study explored if available ACP tools are acceptable for use in LTC by (a) eliciting staff views on the content and format that would support ACP tool usability in LTC (b) examining if publicly available ACP tools include content identified as relevant by LTC home staff. Ultimately this study aimed to identify the potential for existing ACP tools to improve ACP engagement in LTC. Methods A combination of focus group deliberations with LTC home staff (N = 32) and content analysis of publicly available ACP tools (N = 32) were used to meet the study aims. Results Focus group deliberations suggested that publicly available ACP tools may be acceptable for use in LTC if the tools include psychosocial elements and paper-based versions exist. Content analysis of available paper-based tools revealed that only a handful of ACP tools (32/611, 5%) include psychosocial content, with most encouraging psychosocially-oriented reflections (30/32, 84%), and far fewer providing direction around other elements of ACP such as communicating psychosocial preferences (14/32, 44%) or transforming preferences into a documented plan (7/32, 22%). Conclusions ACP tools that include psychosocial content may improve ACP uptake in LTC because they elicit future care issues considered pertinent and can be supported by a range of clinical and non-clinical staff. To increase usability and engagement ACP tools may require infusion of scenarios pertinent to frail older persons, and a better balance between psychosocial content that elicits reflections and psychosocial content that supports communication.


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