I don't know if the following is really true or whether it can be used to say patients with ME/CFS don't want GET and CBT based on GET services and so that should not be what is offered?
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Background:
Somebody sent me this:
Br J Psychiatry. 2002 Dec;181:468-72.
From passive subjects to equal partners: qualitative review of user involvement in research.
Trivedi P, Wykes T.
Full free text:
http://bjp.rcpsych.org/cgi/content/full/181/6/468
I can't say I found it particularly exciting, nor am I recommending people read it.
The quote is from:
How will dissemination occur?
The dissemination of clinical research findings generally occurs only in peer-reviewed journals and during academic conference presentations. These usually have an impact only on a relatively small number of clinicians who are research-oriented, and the Department of Health and funding bodies have stressed that a much wider dissemination process is necessary. In particular, dissemination to users is essential since, in the new consumer orientation of the UK NHS, it is not only evidence-based, randomised, controlled trials that determine what interventions are introduced into clinical practice, but also consumer demand (Department of Health, 1999).
Reference:
Department of Health (1999) Patient and Public Involvement in the New NHS.
London: Department of Health.
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Background:
Somebody sent me this:
Br J Psychiatry. 2002 Dec;181:468-72.
From passive subjects to equal partners: qualitative review of user involvement in research.
Trivedi P, Wykes T.
Full free text:
http://bjp.rcpsych.org/cgi/content/full/181/6/468
I can't say I found it particularly exciting, nor am I recommending people read it.
The quote is from:
How will dissemination occur?
The dissemination of clinical research findings generally occurs only in peer-reviewed journals and during academic conference presentations. These usually have an impact only on a relatively small number of clinicians who are research-oriented, and the Department of Health and funding bodies have stressed that a much wider dissemination process is necessary. In particular, dissemination to users is essential since, in the new consumer orientation of the UK NHS, it is not only evidence-based, randomised, controlled trials that determine what interventions are introduced into clinical practice, but also consumer demand (Department of Health, 1999).
Reference:
Department of Health (1999) Patient and Public Involvement in the New NHS.
London: Department of Health.
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