We are planning a study to understand how patients approaching the end of life (from cancer or other advanced diseases) access medicines for symptom management.

We wish to collect data on issues such as circumstances of new or repeat prescriptions, who was contacted, how, effort and time taken to receive prescription, any incorrect or duplicate medicines received, and satisfaction with information about medicines given at each point of contact.

Does anyone have any experience with this approach or is aware of studies that have reported on medicines access experience in any health care field?

Thank you!    

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