Social impact of the JACO wheelchair-mounted robotic arm on users and their caregivers

Abstract

The efficacious implementation of robotic assistive technologies must be built on a thorough understanding of stakeholders' experiences and perceptions. This study provides an in-depth insight into the experiences and perceptions of users of the JACO wheelchair-mounted robotic arm and those of their caregivers. A sample of JACO users (n = 21; Female : 6; Male : 15) and caregivers (n = 11; Female: 2; Male: 9) participated in individual interviews used to gain qualitative insight into the impact of JACO on their day-to-day lives. Interview transcripts were analyzed using a hybrid deductive-inductive coding process. Thematic analysis was conducted in accordance with the Consortium on Assistive Technology Outcomes Research (CATOR) taxonomy. This article exclusively reports data on the social impact of the JACO wheelchair-mounted robotic arm. In addition, participants completed three questionnaires to gather more objective data for quantitative assessment, these included the Caregiver Assistive Technology Outcome Measure (CATOM), a sociodemographic questionnaire, and a home-based questionnaire to assess the social impact of using JACO. Findings pointed to highly varied experiences among participants, including instances of positive, negative, and absence of effects from the use of JACO. Participants' feedback fell within two broad categories, Human Assistance, and Cost and Use of Resources. This study provides nuanced and varied insight into the spectrum of the social impact of using JACO as perceived by users and their caregivers, highlighting the importance of considering each user as an individual with unique experiences and needs. Continued research is needed to assess the generalizability of these findings.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study was funded by Mitacs university-industry partnership (involving Universite Laval and Kinova Inc)

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethics committee/IRB of Centre integre en sante et service sociaux de la Capitale-Nationale, secteur readaptation et integration sociale (CER-CIUSSCN) gave ethical approval for this work #RIS_2018-608

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

留言 (0)

沒有登入
gif