Physician-Investigator, Research Coordinator, and Patient Perspectives on Dual-Role Consent in Oncology: A Qualitative Study.

ABSTRACT:

Importance

Classic statements of research ethics generally advise against dual-role consent in which physician-investigators seek consent for research participation from patients with whom they have preexisting treatment relationships. Yet dual-role consent is common in clinical oncology research, as studies are often conducted in close relationship with clinical care.

Objective

To explore key stakeholders' perspectives on dual-role consent in clinical oncology trials.

Design, setting, and participants

This qualitative study with 43 participants was conducted at a National Cancer Institute-designated comprehensive cancer center from 2018 to 2022. Semistructured qualitative interviews of physician-investigators, research coordinators, and patients were performed. Respo

SUBMITTER: Morain SR 

PROVIDER: S-EPMC10369198 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature