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Does a central registry for members of the public (i.e. a list of people with contact details) who are interested in taking part in a randomised trial improve recruitment?
A central registry is a list of people, with their contact details, who have expressed an interest in taking part in a randomised trial
- “Would it be better to have a more general conversation with patient groups about adding their names to a registry if they are interested in participating in trials and therefore they would be able to contacted from that registry rather than when they are in hospital or at clinics.”
