Provision of pain care services for people with Parkinson's disease from the perspective of healthcare providers: A qualitative descriptive study

Key Points

• Pain care services for Parkinson's disease appear underreported among healthcare providers, indicating gaps in service delivery.
• The qualitative research approach involved in-depth interviews with healthcare providers to gather insights.
• Findings reveal significant challenges faced by providers in meeting the pain management needs of individuals with Parkinson's disease.
• Implications of this study suggest a need for improved training and resources to enhance pain management services for these patients.

Abstract