Paige S Ryals
Biographic Data
| ID | 8258240 |
|---|---|
| NAME | Paige S Ryals |
| GIVEN NAMES | Paige S |
| FAMILY NAME | Ryals |
| SIGNATURE | RYALS P S |
| AFFILIATIONS | Emory University |
| VERIFIED | No |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 3 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2025 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Disability Community Perspectives on Participation in Research and Studying Positive Health
A paradigm shift in how positive health is framed may enhance its relevance to disabilities. An action plan for researchers is derived as a pragmatic approach to strengthen the relevance, generalizability and impact of their research
Caregiver and clinician perceptions of barriers to cerebral palsy healthcare—mixed methods findings and systems change recommendations
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. Resul…
Synergies, Discrepancies, and Action Priorities
BACKGROUND: Cerebral palsy (CP) clinical research is fraught with challenges, in part due to health-related disparities common among people with disabilities. Perspectives of people with lived experience of CP, clinicians and researchers vary on how to address these disparities. The present initiative explores synergies and discrepancies among stakeholders (n = 212) representing these partner groups in perceived barriers and facilitators to high-…
No prominent works on this page.
Caregiver and clinician perceptions of barriers to cerebral palsy healthcare—mixed methods findings and systems change recommendations
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. Resul…
Synergies, Discrepancies, and Action Priorities
BACKGROUND: Cerebral palsy (CP) clinical research is fraught with challenges, in part due to health-related disparities common among people with disabilities. Perspectives of people with lived experience of CP, clinicians and researchers vary on how to address these disparities. The present initiative explores synergies and discrepancies among stakeholders (n = 212) representing these partner groups in perceived barriers and facilitators to high-…
Disability Community Perspectives on Participation in Research and Studying Positive Health
A paradigm shift in how positive health is framed may enhance its relevance to disabilities. An action plan for researchers is derived as a pragmatic approach to strengthen the relevance, generalizability and impact of their research
Cerebral Palsy and Movement Disorders (3 works) · Cerebral palsy (2 works) · Action (physics (1 works) · Action research (1 works) · Citizen journalism (1 works) · Cognitive reframing (1 works) · Community engagement (1 works) · Community-based participatory research (1 works) · Context (archaeology (1 works) · Disability Rights and Representation (1 works)