The objective of this study was to develop informed consent processes for clinical trials that meet patients’ and surrogates’ needs and expectations in emergency settings.
Project page: Understanding and Improving Informed Consent for Clinical Trials during Health Emergencies
Principal Investigator: Neal Dickert, MD, PhD
Organization: Emory University
Original project title: Integrative Medical Group Visits: A Patient-Centered Approach to Reducing Chronic Pain and Depression in a Disparate Urban Population
HSRProj ID: 20152290
To cite this document, please use: Dickert NW, Mitchell AR, Speight CD, et al. (2020). Understanding and Improving Informed Consent for Clinical Trials during Health Emergencies. Patient-Centered Outcomes Research Institute (PCORI). https://doi.org/10.25302/09.2020.ME.140210638
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