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Journal Article

Citation

Coffey NT, Cassese J, Cai X, Garfinkel S, Patel D, Jones R, Shaewitz D, Weinstein AA. J. Med. Internet. Res. 2017; 19(5): e159.

Affiliation

Center for the Study of Chronic Illness and Disability, George Mason University, Fairfax, VA, United States.

Copyright

(Copyright © 2017, Centre for Global eHealth Innovation)

DOI

10.2196/jmir.7027

PMID

28490418

Abstract

BACKGROUND: In order to meet the challenges of caring for an injured person, caregivers need access to health information. However, caregivers often feel that they lack adequate information. Previous studies of caregivers have primarily focused on either their time and emotional burdens or their health outcomes, but the information needs of caregivers have not been thoroughly investigated.

OBJECTIVE: The purpose of this investigation was to identify the preferred sources of health information for caregivers supporting individuals with injuries and to explore how access to this information could be improved.

METHODS: A total of 32 caregivers participated in semistructured interviews, which were used in order to develop a more in-depth understanding of these caregivers' information needs. Digital audio recordings of the interviews were used for analysis purposes. These audio recordings were analyzed using a thematic analysis or qualitative content analysis. All of participant's interviews were then coded using the qualitative analysis program, Nvivo 10 for Mac (QSR International).

RESULTS: The caregivers endorsed similar behaviors and preferences when seeking and accessing health information. Medical professionals were the preferred source of information, while ease of access made the Internet the most common avenue to obtain information. The challenges faced by participants were frequently a result of limited support. In describing an ideal health system, participants expressed interest in a comprehensive care website offering support network resources, instructive services about the injury and caregiving, and injury-specific materials.

CONCLUSIONS: According to the participants, an ideal health information system would include a comprehensive care website that offered supportive network resources, instructive services about the injury and caregiving, and materials specific to the type of patient injury.


Language: en

Keywords

burns; caregivers; health information, consumer; qualitative research; spinal cord injuries; traumatic brain injury

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