TY - JOUR
T1 - Engaging Veterans, caregivers, and system stakeholders to improve VA home and community-based services
AU - the Elizabeth Dole Center of Excellence for Veteran and Caregiver Research Team
AU - Leykum, Luci K.
AU - Finley, Erin P.
AU - Penney, Lauren S.
AU - Parish Johnson, Julie
AU - Pugh, Jacqueline A.
AU - Noel, Polly H.
N1 - Funding Information:
This work is supported by the Department of Veterans Affairs Health Services Research & Development Service (SDR 18‐313, CIN13‐410) and Geriatrics Research, Education, and Clinical Centers (GRECCs). The views expressed are those of the authors and do not represent an official position of the Department of Veterans Affairs. We thank Dr. Lynda Davis for her partnership and guidance, and the Veterans, caregivers, clinicians, staff, and administrators, who collaborated with us in this work.
Funding Information:
This work is supported by the Department of Veterans Affairs Health Services Research & Development Service (SDR 18-313, CIN13-410) and Geriatrics Research, Education, and Clinical Centers (GRECCs). The views expressed are those of the authors and do not represent an official position of the Department of Veterans Affairs. We thank Dr. Lynda Davis for her partnership and guidance, and the Veterans, caregivers, clinicians, staff, and administrators, who collaborated with us in this work.
Publisher Copyright:
© 2022 Health Research and Educational Trust.
PY - 2022/6
Y1 - 2022/6
N2 - Objective: To understand Veterans', caregivers', and stakeholders' perceptions of home-based and caregiver support services and their suggestions for improvement to better align services with needs. Data Sources: We identified Veterans and caregivers at four EDCoE sites using the VA high-need, high-risk list, representing Veterans who qualify for home-based primary care. We randomly selected Veterans and their caregivers, stratifying by age. We also identified leaders and clinicians involved in clinical service delivery. Study Design: Between February and November 2019, we conducted in-person and telephone interviews and focus groups using semi-structured questions tailored to each group, analyzing them through a rapid qualitative analysis approach and providing real-time feedback to operational partners. Data Collection: Thirty-four Veterans, 24 caregivers, and 39 leaders and clinicians participated. Principal Findings: Respondents identified key categories of experience that could be monitored and improved, including navigating an increasingly complex system, coordinating and communicating across services, and unmet household and financial needs. Veterans and caregivers described quality in terms of reliability, timeliness, standardization, and accountability. Summaries were created to contextualize results and to highlight gaps and opportunities for new measures and policy development. Conclusions: Collaborating with Veterans, caregivers, and stakeholders enables us to understand their daily experiences and to develop meaningful approaches to evaluating services that incorporate their perspectives. Providing regular, actionable feedback to operational partners informs policy and operational initiatives, such as the scope of services and infrastructure for system navigation.
AB - Objective: To understand Veterans', caregivers', and stakeholders' perceptions of home-based and caregiver support services and their suggestions for improvement to better align services with needs. Data Sources: We identified Veterans and caregivers at four EDCoE sites using the VA high-need, high-risk list, representing Veterans who qualify for home-based primary care. We randomly selected Veterans and their caregivers, stratifying by age. We also identified leaders and clinicians involved in clinical service delivery. Study Design: Between February and November 2019, we conducted in-person and telephone interviews and focus groups using semi-structured questions tailored to each group, analyzing them through a rapid qualitative analysis approach and providing real-time feedback to operational partners. Data Collection: Thirty-four Veterans, 24 caregivers, and 39 leaders and clinicians participated. Principal Findings: Respondents identified key categories of experience that could be monitored and improved, including navigating an increasingly complex system, coordinating and communicating across services, and unmet household and financial needs. Veterans and caregivers described quality in terms of reliability, timeliness, standardization, and accountability. Summaries were created to contextualize results and to highlight gaps and opportunities for new measures and policy development. Conclusions: Collaborating with Veterans, caregivers, and stakeholders enables us to understand their daily experiences and to develop meaningful approaches to evaluating services that incorporate their perspectives. Providing regular, actionable feedback to operational partners informs policy and operational initiatives, such as the scope of services and infrastructure for system navigation.
KW - Veterans
KW - caregivers
KW - focus groups
KW - home care services
KW - policy
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U2 - 10.1111/1475-6773.13926
DO - 10.1111/1475-6773.13926
M3 - Article
C2 - 35243641
AN - SCOPUS:85128862100
SN - 0017-9124
VL - 57
SP - 66
EP - 76
JO - Health Services Research
JF - Health Services Research
IS - S1
ER -