Abstract
BackgroundResearch on cerebral palsy (CP) has lacked emphasis on knowledge and treatment practices among caregivers, particularly in low- and middle-income countries where socio-cultural contexts encourage a variety of treatment alternatives. In this study, we explored the beliefs and experiences that motivate care-seeking practices among caregivers of children with CP in Ghana.MethodsSemi-structured interviews were conducted with 25 caregivers, 10 medical providers, and 5 alternative providers in the Greater Accra Region. Participant interviews were analyzed using principles adapted from grounded theory. A conceptual model was constructed to illustrate salient patterns and motivational factors influencing care-seeking practices.ResultsParticipants’ experiences showed that caregivers initially sought physiotherapy and prescription medications from medical providers. Many of them then transitioned to alternative methods to search for a cure or address specific CP symptoms. Over time, most caregivers discontinued both medical and alternative care in favor of at-home treatment. A few withdrew completely from all forms of care. Cost of treatment, caregiver burden, and stigma strongly inhibited care-seeking outside the home.ConclusionAlthough caregivers were open to exploring a variety of treatment options, at-home treatment was preferred by long-time caregivers for its convenience, low cost, and adaptability to patient and caregiver needs.
Highlights
Many of them transitioned to alternative methods to search for a cure or address specific cerebral palsy (CP) symptoms
Caregiver burden, and stigma strongly inhibited care-seeking outside the home
Cerebral palsy (CP) is a neurodevelopmental disability that begins in infancy and persists throughout an individual’s lifespan
Summary
Research on cerebral palsy (CP) has lacked emphasis on knowledge and treatment practices among caregivers, in low- and middle-income countries where socio-cultural contexts encourage a variety of treatment alternatives.
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