Research Ethics

Catalog

• #Informed Consent

  • #Design informed consent process for medical research study. Help me: 1) Write consent document in plain language (8th grade reading level), 2) Explain study purpose, procedures, duration clearly, 3) Describe risks and benefits honestly, 4) Explain voluntary nature and right to withdraw, 5) Address confidentiality and data security, 6) Explain compensation if applicable, 7) Provide contact information for questions, 8) Plan process for obtaining signatures (electronic vs paper)

• #Irb Application

  • #Prepare IRB application for interview study on sensitive topic (sexual assault survivors). Help me: 1) Write clear research protocol with objectives and methods, 2) Design informed consent process with ongoing consent, 3) Address risks (psychological distress) and mitigation strategies, 4) Explain confidentiality protections and data security, 5) Provide recruitment materials and interview protocol, 6) Address vulnerable population considerations, 7) Plan dissemination that protects participants