Caregiver and clinician perceptions of barriers to cerebral palsy healthcare—mixed methods findings and systems change recommendations
Bibliographic Data
| ID | 22073665 |
|---|---|
| Authors | Melissa M Murphy (0000-0002-5957-4944, Emory University), Gavin T Colquitt (0000-0003-3460-1085, Appalachian State University), Paige S Ryals (Emory University), Katie Shin (0009-0006-6229-3576, Emory University), William C Kjeldsen (0009-0002-2861-8972, Emory University), Nathalie L Maitre (0000-0001-8520-9302, Emory University, corresponding author) |
| Year | 2025 |
| Volume | 13 |
| Pages | 1644144-1644144 |
| Publication date | 2025-10-22 |
| Peer Reviewed | Yes |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Frontiers in Public Health (JOURNAL) |
| Journal identifiers | ISSN: 2296-2565 • E-ISSN: 2296-2565 |
| Publisher | Frontiers Media SA (PUBLISHER • CH) |
| DOI | 10.3389/fpubh.2025.1644144 |
| PMID | 41200035 |
| OpenAlex | W4415419004 |
| Language | EN |
| References cited | 35 |
Introduction The present paper is the second in a series of exploration phase efforts toward building and sustaining patient-centered agendas for research and clinical care in CP. Methods Focus group and surveys were used to assess perspectives of caregivers of young children with CP ( N = 19) and clinicians ( N = 102) regarding CP-specific medical care priorities and barriers and facilitators to high quality CP-focused care in Georgia, US. Results Qualitative and quantitative analysis reveal areas of areas of synergy and discrepancy between the two stakeholder groups. Discussion Together stakeholder responses converge on the notion that (1) empowering caregivers to better utilize the resources that do exist and (2) building provider capacity and confidence in efficient delivery of high-quality CP care is critical to drive system changes for improving access and outcomes across the lifespan. Proposed action items for systems change arise from the convergence of caregiver and clinician responses
Cerebral palsy · Perception · Stakeholder · Theory of change · Cerebral Palsy and Movement Disorders · Family and Disability Support Research · Infant Development and Preterm Care
The World Caf in action research settings
Research electronic data capture (Redcap)—A metadata-driven methodology and workflow process for providing translational research informatics support
The Redcap consortium
Interrater reliability
A Coefficient of Agreement for Nominal Scales
Synergies, Discrepancies, and Action Priorities
Strengthening Equitable Access to Care and Support for Children with Cerebral Palsy and Their Caregivers
Designing and Conducting Mixed Methods Research
Member Checking
Parents' Experiences of Health Care for Their Children With Cerebral Palsy
| Citation velocity | historical |
|---|---|
| Highly cited | No |