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Published on: February 16, 2011
"When You Look at This Chart, That Is Not My Whole Life": Caregiver Perspectives to Inform Improved Primary Care
Monique Quinn1, Allison Parsons2, Chidiogo Anyigbo1,3
1Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Insights
Caregiver trust and relationships with healthcare providers are crucial for infant well-child visits (WCVs). Addressing mistrust and social-emotional needs can improve WCV adherence for underserved families.
Area of Science:
- Public Health
- Healthcare Disparities
- Pediatric Care
Background:
- Rising infant and maternal mortality rates necessitate interventions.
- Infant Well Child Visits (WCVs) are key for prevention but are missed disproportionately by low-income and Black families.
- Community caregiver input is vital for effective intervention design.
Purpose of the Study:
- To explore the perspectives of caregivers regarding barriers and facilitators to infant Well Child Visits (WCVs).
- To identify key themes from under-resourced communities to inform intervention strategies.
- To understand the role of trust and interpersonal relationships in healthcare access for infants.
Main Methods:
- Purposeful sampling and interviews with 10 caregivers in Cincinnati, OH.
- Interviews conducted by community peer researchers.
- Thematic analysis of interview transcripts by the research team.
Main Results:
- Most interviewed caregivers (9/10) identified as Black, with children insured by Medicaid.
- Caregivers emphasized the importance of trust, empathy, shared decision-making, and patient-practitioner relationships.
- Mistrust, lack of racial concordance, reliance on community for healthcare decisions, racism, and perceived judgment were significant barriers.
Conclusions:
- Community-informed approaches are essential for intervention development.
- Interpersonal relationships, trust, and social-emotional support are as critical as material resources for WCV adherence.
- Systemic improvements and further research are needed to address healthcare access for infants.
Objective:
Worsening rates of infant and maternal mortality in the United States serve as an urgent call for multi-modal intervention. Infant Well Child Visits (WCVs) provide an opportunity for prevention, however not all infants receive the recommended schedule of visits, with infants of low-income and Black families missing a higher portion of WCVs. Due to diverse experiences and needs of under-resourced communities throughout the United States, caregiver voice is essential when designing improvement efforts.
Methods:
Purposeful sampling and interviewing of 10 caregivers in Cincinnati, OH was performed by community peer researchers. Interview transcripts were evaluated by the research team, with identification of several important themes.
Results:
Nine out of 10 caregivers self-identified as Black. All young children of the interviewed caregivers had Medicaid as their insurance provider. All interviews highlighted rich perspectives on caregiver hopes for their child, family, and selves. Establishing trust through empathy, shared decision making, and the nurturing of interpersonal patient-practitioner relationships is crucial for fostering a positive healthcare experience. Levels of mistrust was perceptibly high across several interviews, with lack of racial concordance between medical provider and family exacerbating the issue for some caregivers. Caregivers voiced a tendency to rely on family and community members for when to seek out health care for their children, and additionally cited racism and perceptions of being rushed or judged as barriers to seeking further care.
Conclusion:
This study emphasizes the importance of being community-informed when considering interventions. Prior research on the topic of missed WCV's often focused on material resource availability and limitations. While that was commented on by caregivers in this study as well, equal-if not more-attention was directed toward interpersonal relationship formation, the presence or absence of trust between practitioner and caregiver, and the importance of social-emotional support for caregivers. We highlight several opportunities for systemic improvements as well as future directions for research.
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