IMPACT: ClinicalTrials.gov

The IMPACT (Instruction in Monitoring, Procedure Documentation and ClinicalTrials.gov) workshop series provides intermediate instruction for faculty, clinical research professionals with two or more years of experience and other study team members. Before attending this session, participants should have either used ClinicalTrials.gov or previously attended ClinicalTrials.gov registration training. This workshop will describe new requirements for registration, updates, use of special informed consent language, results reporting, and protocol uploads in ClinicalTrials.gov. Hands-on activities within ClinicalTrials.gov and group discussions will help participants learn how to avoid common mistakes. Topics include how to draft arms and interventions, translating protocol aims into specific outcome measures, and results reporting for different clinical trial models.

Duration: 1 - 4 hours

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Free