Exact(4)
Our findings highlight how trial practitioners need to discuss 50 potentially threatening information with parents to identify their priorities 49 and clarify related aspects of written trial information to assist understanding and decision-making.
To begin to answer these questions, this paper draws on insights from empirical data from an online survey on the views and experiences of clinical trial practitioners working in paediatric and neonatal emergency care settings.
The practice and participant retention strategy is based around actively maintaining contact with all trial practitioners throughout the study (there will be fortnightly emailed updates and regular newsletters), showing their time is valued (through CPD and remuneration).
10 11 12 If, for example, it is unclear whether patients with particular comorbidities were excluded from a trial, practitioners using the trial report for medical decision making cannot know whether the results can apply to their patients with one of these comorbidities.
Similar(55)
Some clinical trials practitioners dislike the follow-up forms and the quantity of data requested.
Clinical trials practitioners like the study as it is easy to recruit to, and fits with routine follow-up regimes.
Despite the lack of evidence from clinical trials practitioners that had attended presentations about the WSP were keen advocates of the program.
While looking forward to the results of ongoing trials, practitioners can be reassured that the unexpected association reported in the SAVOR TIMI study has not been confirmed in the real world.
Clinical data are obtained from the patient medical records by the Clinical Trials Practitioner (CTP) at each recruiting centre and entered onto a standard clinical trials data form (additional file 3).
II) Retrospective searches of computerised records of local General Practices will be conducted by practice staff with the assistance of the Clinical Trials Practitioner (CTP) from the Northern Ireland Primary Care Research Network (PCRN).
A follow-up data form is completed by the Clinical Trials Practitioner (CTP) at diagnosis, 3, 6, 9, 12, 15, 18, 21, 24, 27, and 30 months, and then every 6 months until 84 months from the date of commencement of CAB.
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