I remember a cryptic comment from last year re the FOI requests to the effect that Peter White was handling the same dataset for this study and therefore available to extract info. It may have been prior to his retirement - but if he is not doing it - who is?
I could be going completely barmy today, so apologies in advance, but is there not a study/ initiative tracing PACE trial participants currently ? I have a faint memory of something mentioned last year.
Yes, that makes sense , but there must be other ways of achieving this.
If you had to have a single centre why London- why not somewhere geographically more central?
Why London? Why not multicentred to enable wider input ?
Whilst there may have been some thought re patient engagement this is not coming over.
If you want meaningful engagement, with a group that will have their health impacted through travel, then skype participation seems a no brainer, but...
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