Objective Dissemination of research findings is central to research integrity and promoting
discussion of new knowledge and its potential for translation into practice and policy. We …

As clinical trials end, little is understood about how participants exiting from clinical trials
approach decisions related to the removal or post-trial use of investigational brain implants …

Background: The Federal Policy for the Protection of Human Subjects—the Common Rule—
was revised in 2017 to reduce administrative burdens for low-risk research while enhancing …

Health research participants want the results of the studies in which they participate but do
not typically receive them. Researchers generally express support for sharing results with …

Background Although research participants are generally interested in receiving results from
studies in which they participate, health researchers rarely communicate study findings to …

Many research studies have offered ethical guidelines for the recruiting of participants,
solicitation of informed consent, and harvesting of data from communities and individuals …

There is a growing need to better capture comprehensive, nuanced, and multi-faceted
qualitative data while also better engaging with participants in data collection, especially in …

Responsive caregiving is associated with secure attachment and positive child
developmental outcomes. However, there is some debate on whether responsive caregiving …

Objective Returning aggregate study results is an important ethical responsibility to promote
trust and inform decision making, but the practice of providing results to a lay audience is not …

Statistical power in cognitive neuroimaging experiments is often very low. Low sample size
can reduce the likelihood of detecting real effects (false negatives) and increase the risk of …