Electronic Informed Consent in the Multi-Arm Optimization of Stroke Thrombolysis Trial
eConsent in MOST was associated with higher individual site enrollment, higher remote consent rates, and improved consent documentation adherence over paper consent. Our study outlines the potential advantages of eConsent adoption in future acute ischemic stroke clinical trials and stroke research networks.
Authors
- Opeolu M Adeoye (ORCID: https://orcid.org/0000-0001-8666-5369)
- Christopher Streib (ORCID: https://orcid.org/0000-0002-1119-757X)
- James C. Grotta (ORCID: https://orcid.org/0000-0002-3667-4248)
- Anthony Rogers (ORCID: https://orcid.org/0000-0001-7233-0496)
- Akash Roy (ORCID: https://orcid.org/0000-0001-6506-6156)
- Colin P. Derdeyn (ORCID: https://orcid.org/0000-0002-5932-2683)
- Abbey Staugaitis
- Pooja Kumari Khatri (ORCID: https://orcid.org/0000-0002-7344-8266)
- Joseph P. Broderick (ORCID: https://orcid.org/0000-0002-7323-7709)
- Karen Stalin
- Oladi Bentho
- Ian Rines
- Andrew D. Baretto
Institutions
- University of Minnesota (US)
- Memorial Hermann (US)
- Medical University of South Carolina (US)
- Washington University in St. Louis (US)
- University of Virginia (US)
- University of Cincinnati (US)
- The University of Texas Health Science Center at Houston (US)
Publication Details
- Journal
- Stroke
- Published
- 2025-04-16
- DOI
- https://doi.org/10.1161/strokeaha.124.049369
- Citations
- 2
- Primary Topic
- Ethics in Clinical Research
- Type
- article
- Field-Weighted Citation Impact
- 3.76