While strategies to recruit and consent participants are usually detailed in clinical research protocols, protocols are often silent on how researchers plan to communicate with participants after they have started in the project. As these post-consent communication activities are rarely discussed in the ...
In a cohort of 6,785 participants from the All of Us Research Program whose sleep was monitored by a Fitbit over a median of 4.5 years, sleep duration, stages and irregularity were associated with the incidence of obesity and a number of cardiovascular and psychological disorders. ...
The rapid emergence of novel cannabinoids outpaces systematic research necessary to inform regulations and harm reduction. Empirical evidence is needed to guide policies, practices, and education of consumers. Product manufacturers, social media participants, and cannabis oriented on-line news sources have...
the way that the participants'brain cells connect began to be like those of memory champions compared to scans (描) taken before training.Researchers believe this could be responsible for their increased memory.But what makes this research so fascinating is that it seems to prove that the talent...
BN, YG, HLL, WQL, JCS were the main participants in the consensus discussion, formulating the consensus framework and proposing to update the main points. SYL was the secretary of the consensus group and the first writing author of the manuscript. Other experts participate in literature review,...
Policy Scope of Policy This Clinical Policy Bulletin addresses evoked potential studies. Medical Necessity Evoked Potential Studies Aetna considers evoked potential studies medically necessary for the following indications: Somatosensory evoked potentials (SEPs, SSEPs) or dermato-sensory evoked potentials (DS...
Are participants in the Medical Student Research Programme continuing to engage in research?doi:10.4045/tidsskr.18.0266BJERKREIM, ANNA THERESEESKERUD, INGEBORGGUTTORMSEN, ANNE BERITMLLER, KARL ERIKJournal of the Norwegian Medical Association / Tidsskrift for Den Norske Laegeforening...
Research design This is a single-center observational study. Participants needed to use the eSource method and the non-eSource method to complete two workflows. The goal of this study is to evaluate the impact of the two processes on source data collection (EMR writing) and data transcription...
Ethical approval was obtained from the Universiti Malaya Research Ethics Committee (Reference Number: UM.TNC2/UMREC_2486). Informed consent was obtained from all participants. Participation was voluntary. Consent for publication Not applicable. Competing interests The authors declare no competing interests...
Questionnaires remain one of the most common forms of data collection in epidemiology, psychology and other human-sciences. However, results can be badly affected by non-response. One way to potentially reduce non-response is by sending potential study p