| Literature DB >> 27630213 |
Alinne Z Barrera1, Laura B Dunn2, Alexandra Nichols1, Sonia Reardon1, Ricardo F Muñoz1,2,3.
Abstract
Ethical principles in conducting technology-based research require effective and efficient methods of ensuring adequate informed consent. This study examined how well participants understood the informed consent form for an online postpartum depression trial. Pregnant women ( N = 1,179) who consented to the trial demonstrated an understanding of the purpose (86.1%) and procedures of the study (75.8%), and the minimal risks associated with answering sensitive questions online (79%). Almost all (99.6%) understood that psychological treatment was not offered. Participants with current depression incorrectly indicated that participation would replace current psychological treatment relative to participants with a lifetime or no depression history (19.6% vs. 13.5 % vs. 10.4%, respectively) and that there were no associated risks with participation (29.6% vs.17.6% vs. 16.7%, respectively). Findings provide initial evidence that most individuals who seek online psychological resources are informed consumers.Entities:
Keywords: Internet; clinical trials; informed consent; maternal; online; postpartum depression; pregnancy; prevention; research ethics
Mesh:
Year: 2016 PMID: 27630213 PMCID: PMC5334448 DOI: 10.1177/1556264616668974
Source DB: PubMed Journal: J Empir Res Hum Res Ethics ISSN: 1556-2646 Impact factor: 1.742