None listed
Conditions
Brief summary
The aim of this study it to determine the best way for the NIHR HTA programme to engage with clinical experts to ensure we prioritise the most important research questions for the NHS.
Interventions
Clinical experts who have agreed to provide advise to the NIHR HTA programme's vignette process (used to help prioritise questions for pragmatic clinical research) will be sent either a short (1 page- the intervention)) or long (up to 10 page - usual control) paper, and asked to provide advice on it using either a structured form (control) or free text (intervention) to reply. As a 2x2 factorial study the randomisations are short v long paper; and structured form v free text It is anticipated that the control group options (long paper and structured form) will take less than an hour to complete, with the intervention options (short paper and free text) shortening the required time for the participant.
Sponsors
Study design
Eligibility
Inclusion criteria
Vignettes - all vignettes prepared during the Autumn 2013 and Spring 2014 prioritisation rounds of the NIHR HTA Programme Experts - all clinical experts included to comment on the prepared vignettes
Exclusion criteria
Vignettes - those which ask a methodological, rather than clinical question - vignettes where the responsible CA does not want external experts - Vignettes which have been through previous external review, other than as a panel topic Experts - Non-clinical experts, eg PPI advisors, methodologists. Clinical-Academics count as clinical experts. The final decision as to whether an advisor is 'clinical' rests with the Steering Group responsible for the vignette, who may take advice from the relevant CA - People who have provided advice on the panel topic from which the vignette was derived - Current and previous members of HTA prioritisation and TIDE panels