Data collection in pragmatic trials, should we use eCRF or existing routine systems (e.g. EHR)?
A series of eight papers has been published in the Journal of Clinical Epidemiology.
Introduction: Pragmatic trials and Real World Evidence
Selection and inclusion of usual care sites
Participant eligibility, recruitment and retention
Challenges of informed consent
Questions, comparators and treatment strategies
Outcome selection and measurement
Monitoring safety and trial conduct
Read more on data collection in our JCE paper series, which discusses data collectiokn in pragmatic trials.
For a summary, please click here.
For more information on data management in pragmatic trials, please click here.
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