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Sixty-six percent of children had more than one caregiver, with caregiver defined as someone who gives the child medication.
> Acceptability has previously been defined as "an overall ability of the patient and caregiver (defined as 'user') to use a medicinal product as intended (or authorised)" [ 1].
A family caregiver, defined as the person who non-professionally takes care and supports the patient for most of the time, will be identified by the patient.
9 The inability of a stroke survivor with PSS to perform basic activities exerts a considerable burden on the informal caregiver, defined as someone close to the stroke survivor who is not hired to provide caregiving services.
In the intake interview, the caregiver (defined as the individual who knows most about asthma care for the child) was asked about family demographics, child and family asthma history, access to health care, exposure to smoking, and medication usage, with questions taken from NCICAS when possible to facilitate comparability [ 20].
The data set included relevant information on patient's socio-demographic characteristics and health status, as well as some information on their primary caregiver (defined as the person who spent most of the time with the elder during their hospital stay, and knew most of the information regarding the health status of the patient) [ 14].
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Health care personnel, patients, and their caregivers (defined as tutors, accompanying persons and visitors) were systematically invited to participate in the study.
The participants of interest will be caregivers (defined as parents, legal guardians or other persons assuming the parental role) to whom information or education about vaccination is given.
The VOICE Study is a multi-site randomized controlled trial designed to facilitate communication about prognosis and healthcare decision making among oncologists, patients with advanced cancer, and their caregivers (defined as family, friends, or other non-professionals who are involved in their care).
Informal caregivers (defined as " a person who has significant responsibility for managing the well-being of a person diagnosed with schizophrenia in an unpaid capacity" [ 6] ) provide an important service by reducing the need for formal care and the burden upon healthcare systems [ 7].
Future work should examine the relationship between WBVs and unmet need among Medicaid-enrolled infants and clarify how caregivers define unmet need (e.g., primary versus specialty care).
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