Sly Saint
Senior Member (Voting Rights)
One of the biggest problems with Esther Crawleys work is that she never really says what her 'hypothesis' is. She just appears to think that her treatment works (most of the time), the kids are all happy and that's it.Is the idea generally that you try and disprove your hypothesis, not go out if your way to reinforce it ?
eta:
with reference to my last comment:From Reviewer 1's comments on the first draft, she warns about high rates of increase of exercise, given that subjects have ME/CFS!
://bhttpsmjopen.bmj.com/content/bmjopen/6/7/e011255.reviewer-comments.pdf Page 2
"P 8, Lines 4 and 29-30: A progression of 10-20% per week in physical activity is regarded as standard for healthy adults. Other CFS research suggests that progression for CFS patients should be a lot less or at least self-paced with periods of no progression if symptomatic. Can the authors explain why the 10-20% progression was chosen and support this with references from CFS literature?"
Crawley et al's response is:
"2) A progression of up to 20% is the guidance provided by the National Institute of Clinical Excellence1 and is standard practice in the UK. This is also consistent with the PACE trial, the largest trial done to date. We have now included a reference to NICE guidelines and the PACE trial, the protocol now reads: “The intervention will encourage children and adolescents to find a baseline level of exercise which will be increased slowly (by 10-20% a week, as per NICE guidance1 and the PACE trial2)”.
the real reason is it's what they do at her clinic
"
When can I increase my activity levels?
When you have managed 2 weeks of the same activity daily, you can start to increase by 10% a week."
http://www.ruh.nhs.uk/patients/serv...tric_cfs_me/documents/CFSEnergyManagement.pdf
eta2: also don't forget Crawley was a key advisor for the 2007 NICE guidelines; I don't what the 'rules' re increasing activity %s for GET before that were(?).
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