Abdool Karim, Q., Abdool Karim, S. S., Coovadia, H. M., & Susser, M. (1998). Informed consent for HIV testing in a South
African hospital: Is it truly informed and truly voluntary?. American Journal of Public Health, 88(4), 637-640.
Informed consent (adults), Voluntariness and self-efficacy, Adults (other), People living with HIV, People at risk for or with other STIs, Survey research, Health-care facilities, South Africa, Quantitative (QT)
Agnarson, A. M., et al. (2013). Antiretroviral Treatment Knowledge and Stigma – Implications for Programs and HIV Treatment Interventions in Rural Tanzanian Populations. PLoS ONE 8(1): e53993.
Informed consent (adults), Stigma, Adults (other), People at risk for HIV, People at risk for or with other STIs, People living with HIV, Survey research, Community-engaged research,Community organizations, Tanzania, Quantitative (QT)
Akkad, A., Jackson, C., Kenyon, S., Dixon-Woods, M., Taub, N., & Habiba, M. (2006). Patients’ perceptions of written consent: questionnaire study. BMJ: British Medical Journal, 333(7567), 528.
Informed consent (adults), Adults (other), Survey research, Health-care facilities, England, Quantitative (QT)
Brody, H., Croisant, S. A., Crowder, J. W., & Banda, J. P. (2015). Ethical issues in patient-centered outcomes research and comparative effectiveness research: a pilot study of community dialogue. Journal of Empirical Research on Human Research Ethics, 10 (1), 22-30.
Multicultural competence, Adults (other), Community organizations, United States, Qualitative (QL)
Couper, M. P., Singer, E., Conrad, F. G., & Groves, R. M. (2008). Risk of disclosure, perceptions of risk, and concerns about privacy and confidentiality as factors in survey participation. Journal of official statistics, 24(2), 255-275.
Confidentiality and privacy, Research risks and benefits, Research trust and mistrust, Adults (other), Survey research, United States, Quantitative (QT)
Couper, M. P., & Singer, E. (2009). The role of numeracy in informed consent for surveys. Journal of empirical research on human research ethics: JERHRE,4(4), 17.
Confidentiality and privacy, Informed consent (adults), Adults (other), Online and social media research, Online web panel, United States, Quantitative (QT)
Deng, J., Qian, M., Gan, Y., Hu, S., Gao, J., Huang, Z., & Zhang, L. (2015). Emerging practices of counseling and psychotherapy in China: ethical dilemmas in dual relationships. Ethics and Behavior, 26 (1), 63-86.
Multicultural competence, Research misconduct, Therapeutic misconception, Adults (other), Survey research, Health-care facilities, China, Qualitative (QL)
DuBois, J. M., O’Leary, C. C., & Cottler, L. B. (2009).The attitudes of females in drug court toward additional safeguards in HIV prevention research. Prevention Science, 10(4), 345-352.
Informed consent (adults), Research risks and benefits, Adults (other), Incarcerated, detained, or previously incarcerated individuals, People at risk for HIV, People at risk for or with other STIs, People at risk for or with other substance abuse addictions, People who inject drugs, Community-engaged research, Prisons, United States, Qualitative (QL)
Eisingerich, A. B., et al. (2012). Attitudes and Acceptance of Oral and Parenteral HIV Preexposure Prophylaxis among Potential User Groups: A Multinational Study. PLoS ONE 7(1): e28238.
Research risks and benefits, Stigma, Adults (other), People at risk for HIV, People at risk for or with other STIs, People involved in sex work, People who inject drugs, Sexual and gender minorities, Community-engaged research, Community organizations, Health-care facilities, Botswana, India, Kenya, Peru, South Africa, Uganda, Ukraine, Quantitative (QT)
El-Wakeel, H., Taylor, G. J., & Tate, J. J. T. (2006). What do patients really want to know in an informed consent procedure? A questionnaire-based survey of patients in the Bath area, UK. Journal of medical ethics, 32(10), 612-616.
Informed consent (adults), Research risks and benefits, Adults (other), Clinical trials,Survey research, Health-care facilities, England, Quantitative (QT)
Fisher, C. B. (2010). Enhancing HIV Vaccine Trial Consent Preparedness Among Street Drug Users. Journal of Empirical Research on Human Research Ethics, 5 (2), 65-80.
Informed consent (adults), Research trust and mistrust, Adults (other), People at risk for HIV, People at risk for or with other STIs, People who inject drugs, Clinical trials, Neighborhoods, United States, Mixed methods (MM)
Forman, R. F., Bovasso, G., Clark, C., McNicholas, L., Royer-Malvestuto, C., Weinstein, S., & Woody, G. (2002). Staff beliefs about drug abuse clinical trials. Journal of Substance Abuse Treatment, 23 (1), 55-60.
Therapeutic misconception, Voluntariness and self-efficacy, Adults (other), Clinical trials, Ethics education, Health-care facilities, United States, Quantitative (QT)
Franrenet, S., Moutel, G., Raffi, F., Dabis, F., Bruyand, M., Hervé, C., & … Duchange, N. (2011). Information that should be given to HIV cohort participants during ongoing research: The viewpoints of patient representatives and research professionals. Journal Of Empirical Research On Human Research Ethics, 6(4), 76-83.
Investigator practices and perspectives, Adults (other), People at risk for or living with other STIs, People living with HIV, Clinical trials, Health-care facilities, France, Mixed methods (MM)
Hall, M. A., Camacho, F., Lawlor, J. S., DePuy, V., Sugarman, J., & Weinfurt, K. (2006). Measuring trust in medical researchers. Medical care, 1048-1053.
Confidentiality and privacy, Research trust and mistrust, Voluntariness and self-efficacy,Adults (other), Survey research, Health-care facilities, United States, Quantitative (QT)
Lairumbi, G. M., Michael, P., Fitzpatrick, R., & English, M. C. (2012). Forms of benefit sharing in global health research undertaken in resource poor settings: A qualitative study of stakeholders views in Kenya. Philosophy, Ethics, and Humanities in Medicine, 7(7).
Research risks and benefits, Adults (other), Community Advisory Board, Investigators, IRB members, Policy makers, Clinical trials, Health-care facilities, South Africa, Qualitative (QL)
Lakes, K. D., Vaughan, E., Jones, M., Burke, W., Baker, D., & Swanson, J. M. (2012). Diverse perceptions of the informed consent process: Implications for the recruitment and participation of diverse communities in the National Childrens Study. American Journal of Community Psychology, 49, 215-232.
Assent and self-consent (children and adolescents), Informed consent (adults), Multicultural competence, Research risks and benefits, Children, Adults (other), United States, Qualitative (QL)
Länsimies‐Antikainen, H., Laitinen, T., Rauramaa, R., & Pietilä, A. M. (2010). Evaluation of informed consent in health research: a questionnaire survey. Scandinavian Journal of Caring Sciences, 24(1), 56-64.
Informed consent (adults), Adults (other), Clinical trials, Health-care facilities, Finland, Quantitative (QT)
Oliver, J. M., Slashinski, M. J., Wang, T., Kelly, P. A., Hilsenbeck, S. G., & McGuire, A. L. (2011). Balancing the risks and benefits of genomic data sharing: genome research participants’ perspectives. Public Health Genomics, 15(2), 106-114.
Confidentiality and privacy, Informed consent (adults), Research risks and benefits, Research trust and mistrust, Adults (other), Parents, Clinical trials, Health-care facilities, United States, Mixed methods (MM)
Pearson, C. R., Parker, M., Fisher, C. B., & Moreno, C. (2014). Capacity Building from the Inside Out: Development and Evaluation of a CITI Ethics Certification Training Module for American Indian and Alaska Native Community Researchers. Journal Of Empirical Research On Human Research Ethics, 9(1), 46-57.
Multicultural competence, Research risks and benefits, Adults (other), Community-engaged research, Ethics education, Community organizations, United States, Mixed Methods (MM)
Roberts, L. W., Warner, T. D., Brody, J. L., Roberts, B., Lauriello, J., & Lyketsos,C. (2002). Patient and psychiatrist ratings of hypothetical schizophrenia research protocols: assessment of harm potential and factors influencing participation decisions. American Journal of Psychiatry, 159(4), 573-584.
Informed consent (adults), Adults (other), Adults with neurological disorders, Clinical trials, Health-care facilities, United States, Mixed methods (MM)
Roessler, B. J., Steneck, N. H., & Connally, L. (2015). The MICHR genomic DNA BioLibrary: an empirical study of the ethics of biorepository development. Journal of Empirical Research on Human Research Ethics, 10 (1), 37-48.
Informed consent (adults), Research risks and benefits, Adults (other), Health-care facilities, United States, Quantitative (QT)
Rubright, J. D., Cary, M. S., Karlawish, J. H., & Kim, S. Y. (2011). Measuring how people view biomedical research: Reliability and validity analysis of the Research Attitudes Questionnaire. Journal of Empirical Research on Human Research Ethics, 6(1), 63-68.
Confidentiality and privacy, Research trust and mistrust, Stigma, Adults (other), Online and social media research, Online web panel, United States, Quantitative (QT)
Silaigwana, B., & Wassenaar, D. (2015). Biomedical research ethics committees in Sub-Saharan Africa: a collective review of their structure, functioning, and outcomes. Journal of Empirical Research on Human Research Ethics, 10 (2), 169-184.
IRB practices and perspectives, Adults (other), IRB members, Clinical trials, Educational institutions, Health-care facilities, South Africa, Mixed Methods (MM)
Singer, E., & Couper, M. P. (2008). Do incentives exert undue influence on survey participation? Experimental evidence. Journal of empirical research on human research ethics: JERHRE, 3(3), 49-56.
Research risks and benefits, Adults (other), Online and social media research, Online web panel, United States, Quantitative (QT)
Tsang, T. S. M., Jones, M., & Meneilly, G. S. (2015). Analysis of research ethics board approval times in an academic department of medicine. Journal of Empirical Research on Human Research Ethics, 10 (2), 145-150.
IRB practices and perspectives, Adults (other), IRB members, Clinical trials, Educational institutions, Canada, Quantitative (QT)
Varas-Diaz, N., Negron, S. S., Neilands, T. B., Bou, F. C., & Rivera, S. M. (2010). Stigmatization of illicit drug use among Puerto Rican health professionals in training. Puerto Rico Health Sciences Journal, 29(2), 109-116.
Stigma, Adults (other), People at risk for or with substance use addictions, Health-care facilities, Puerto Rico, Mixed Methods (MM)
Vreeman, R., Kamaara, E., Kamanda, A., Ayuku, D., Nyandiko, W., Atwoli, L., & … Braitstein, P. (2012). A qualitative study using traditional community assemblies to investigate community perspectives on informed consent and research participation in western Kenya. BMC Medical Ethics, 1323.
Informed consent (adults), Adults (other), Community Advisory Board, Community-engaged research, Community organizations, Kenya, Qualitative (QL)
Yessis, J. L., et al (2012). Development of a Research Participants’ Perception Survey to Improve Clinical Research. CTS Journal, 5(6): 452-460.
Informed consent (adults), Investigator practices and perspectives, Investigators, Adults (other), Clinical trials, Educational institutions, Canada, Quantitative (QT)
