J Empir Res Hum Res Ethics

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  Publication Venue For

  • In-Home Passive Sensor Data Collection and Its Implications for Social Media Research: Perspectives of Community Women in Rural South Africa..  15:97-107. 2020
  • Perspectives on Electronic Informed Consent From Patients Underrepresented in Research in the United States: A Focus Group Study..  13:338-348. 2018
  • Perceptions of Equipoise, Risk-Benefit Ratios, and "Otherwise Healthy Volunteers" in the Context of Early-Phase HIV Cure Research in the United States: A Qualitative Inquiry..  13:3-17. 2018
  • Are Well-Informed Potential Trial Participants More Likely to Participate?.  12:363-371. 2017
  • Evidence-Based Strategies for Shortening Informed Consent Forms in Clinical Research..  12:14-25. 2017
  • Developing a Framework for Evaluating Ethical Outcomes of Good Participatory Practices in TB Clinical Drug Trials..  11:203-213. 2016
  • Navigating risks and professional roles: research with lesbian, gay, bisexual, trans, and queer young people with intellectual disabilities..  7:20-33. 2012
  • The potential influence of Internet-based social networking on the conduct of clinical research studies..  7:71-80. 2012