TY  - JOUR
AU  - Coffey, Nathan T
AU  - Cassese, James
AU  - Cai, Xinsheng
AU  - Garfinkel, Steven
AU  - Patel, Drasti
AU  - Jones, Rebecca
AU  - Shaewitz, Dahlia
AU  - Weinstein, Ali A
PY  - 2017
DA  - 2017/05/10
TI  - Identifying and Understanding the Health Information Experiences and Preferences of Caregivers of Individuals With Either Traumatic Brain Injury, Spinal Cord Injury, or Burn Injury: A Qualitative Investigation
JO  - J Med Internet Res
SP  - e159
VL  - 19
IS  - 5
KW  - traumatic brain injury
KW  - burns
KW  - spinal cord injuries
KW  - caregivers
KW  - health information, consumer
KW  - qualitative research
AB  - 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. 
SN  - 1438-8871
UR  - http://www.jmir.org/2017/5/e159/
UR  - https://doi.org/10.2196/jmir.7027
UR  - http://www.ncbi.nlm.nih.gov/pubmed/28490418
DO  - 10.2196/jmir.7027
ID  - info:doi/10.2196/jmir.7027
ER  -