Gesundheitsforschung Wenn Sie die einzelnen Literatureinträge auswählen, bekommen Sie eine Zusammenfassung und weitere Informationen.
Buyx, A. (2017). Forschungsethische Implikationen von Big Data im Gesundheitsbereich: die Stellungnahme des Deutschen Ethikrats von November 2017. Forschung, 3+4, 77–84. Cato, K. D., Bockting, W., & Larson, E. (2016). Did I Tell You That? Ethical Issues Related to Using Computational Methods to Discover Non-Disclosed Patient Characteristics. Journal of Empirical Research on Human Research Ethics, 11(3), 214–219. https://doi.org/10.1177/1556264616661611 De Oliveira, L. L. H., Vissoci, J. R. N., Machado, W. de L., Rodrigues, C. G., & Limkakeng, A. T. (2017). Are Well-Informed Potential Trial Participants More Likely to Participate? Journal of Empirical Research on Human Research Ethics, 12(5), 363–371. https://doi.org/10.1177/1556264617737163 Flicker, S., Travers, R., Guta, A., McDonald, S., & Meagher, A. (2007). Ethical Dilemmas in Community-Based Participatory Research: Recommendations for Institutional Review Boards. Journal of Urban Health : Bulletin of the New York Academy of Medicine, 84, 478–493. https://doi.org/10.1007/s11524-007-9165-7 Lathan, H. S., Kwan, A., Takats, C., Tanner, J. P., Wormer, R., Romero, D., & Jones, H. E. (2023). Ethical considerations and methodological uses of Facebook data in public health research: A systematic review. Social Science & Medicine, 322, 115807. https://doi.org/10.1016/j.socscimed.2023.115807 Leonelli, S., Lovell, R., Wheeler, B. W., Fleming, L., & Williams, H. (2021). From FAIR data to fair data use: Methodological data fairness in health-related social media research. Big Data & Society, 8(1), 20539517211010310. https://doi.org/10.1177/20539517211010310 Meier, A. (2018). Alles eine Frage der digitalen Autonomie? Die Rolle von Autonomie in der digitalen Kommunikation für psychologische Grundbedürfnisse und psychische Gesundheit im Alltag. Medien & Kommunikationswissenschaft, 66(4), 407–427. https://doi.org/10.5771/1615-634X-2018-4-407 Norval, C., & Henderson, T. (2020). Automating Dynamic Consent Decisions for the Processing of Social Media Data in Health Research. Journal of Empirical Research on Human Research Ethics, 15(3), 187–201. https://doi.org/10.1177/1556264619883715 Rüdiger, S., & Dayter, D. (2017). The ethics of researching unlikeable subjects. Applied Linguistics Review, 8(2/3), 251–269. Communication & Mass Media Complete. http://search.ebscohost.com/login.aspx?direct=true&db=ufh&AN=123562776&site=ehost-live Rothstein, M. A. (2015). Ethical Issues in Big Data Health Research: Currents in Contemporary Bioethics. Journal of Law, Medicine & Ethics, 43(2), 425–429. https://doi.org/10.1111/jlme.12258 Samuel, G., Derrick, G. E., & van Leeuwen, T. (2019). The Ethics Ecosystem: Personal Ethics, Network Governance and Regulating Actors Governing the Use of Social Media Research Data. Minerva, 57(3), 317–343. https://doi.org/10.1007/s11024-019-09368-3 Schaarschmidt, N. (2018). Media Ethics in Research on Video-Based Mental Health Care. In F. M. Dobrick, J. Fischer, & L. M. Hagen (Eds.), Research Ethics in the Digital Age (pp. 137–142). Springer VS. https://doi.org/10.1007/978-3-658-12909-5_14 Spellecy, R., Eve, A. M., Connors, E. R., Shaker, R., & Clark, D. C. (2018). The Real-Time IRB: A Collaborative Innovation to Decrease IRB Review Time. Journal of Empirical Research on Human Research Ethics, 13(4), 432–437. https://doi.org/10.1177/1556264618780803 Zoller, H. M., Fujishiro, K., Mobley, A., & Lehman, E. (2015). Perspectives on Communication and Participation in Research Notification Focus Groups. Health Communication, 30(10), 986–1000. Communication & Mass Media Complete. http://search.ebscohost.com/login.aspx?direct=true&db=ufh&AN=108302816&site=ehost-live