Why data from PACE trial author and London GET clinic is dubious and does not reflect real ME/CFS. 2021 paper attempts to show GET benefits = gains made on fatigue scale happen in 1st 4 hours/sessions then dont continue to normal levels. tandfonline.com/doi/full/10.10…
92 patients data since 2002 (almost 20 years) including 20 drop-outs still used as data. To take an ME/CFS patient and have them drop fatigue by 4th session may be an act of changing perception. Why then do patients not seem to be returning to normal fatigue levels by the end?
This paper can only be judged as an attempt by a PACE author to sure up evidence for GET use in the face of the impending dropping of GET by NICE, by clubbing together data from as many patients as could be mustered from their clinic over 20 years, no treatment uniformity at all.
I will explain this, you take ambulatory patients, not sicker ME/CFS patients, you take a broad criteria to ME/CFS< only 70% in this cohort met the loose Oxford Criteria; you tell patient to change how they see their fatigue session 1-4 then measure! No comparison group at all.
Some patients had 2 session, some had 15 sessions of GET - making this paper redundant other than as a historical record of how GET is applied to patients in clinic.
Where is the sit to stand test results? again, like in the PACE trial itself, these athors pick out the data they want you to see whilst keeping other test results from us - why perform a sit to stand test and not include the results?
patients were offered between 12 and up to 18-20 sessions depending on if they took extras - so why then do many only make less than 12, some only 2 sessions (why did circa 35 patients not reach 12+ sessions out of the 92)?
SF-36 physical function scale - we see between GET session 1 and 7 (most of treatment) mean stays the same! only between 7 and end of treatment 12-20 sessions does it pop up a bit, but this may be the remainers, the weller patients, pre-GET session 12 almost 1/3 stop as per last
do we know how many patients actually made up the end of treatment or follow up data out of 92n - I cant see it, authors dont appear to include numbers of patients in these slides
so if I am right, even if we accept a rough figure of 60 patients were used for data on SF-36 to derive this follow up data, avg scores went from 45 to 55s, still far below normal - so where are the 22% of patients who should fully recover according to the PACE trial run by same
Found it - wait for it, follow-up data, whether pure of combined, was only available for 18 patients for SF-36 scores at 3 months follow up - in a clinic of a PACE trial author, which claims to have seen patients since 2002 treating them with GET. 18 patients data !
where is dose effect: take ME/CFS patients who are hypothesied tobe deconditioned and afraid of exercise, give 4 hours of GET and see benefit but not a dose effect with more GET over a year of thearpy? does not add up - other than initial treatment effect and other biases
Here is how the authors pondered the fact most gains happen between session/hour 1-4: they say this mirrors CBT, so whether its CBT or GET 1/4 of patients return to normal levels of fatigue within 4 hours - really? what sort of ME patients are these - 1-4 hours to cure MEfatigue?
To make my point even clearer lets look back at the nurse-led CBT-GET trial that also failed to cure ME/CFS-FINE Trial 2010. Note the same pattern, all 3 treatments, blue-line CBT-GET also the green usual GP care all 3 improved fatigue: no care improves fatigue? = treatment bias
Final statement: strong treatment effect biases; no controls; researchers with strong treatment bias; physical test data omitted; missing data manipulated statistically; high drop out rates; data on small numbers of patients; no external replication; an uncertain patient cohort.
Authors conclusion: we cant get the same big recovery results using GET in our clinic as we got in our trial eg PACE, we cant explain why; we still think GET is effective but very modest gains, we only have a small number of patients' data at 3 month follow-up n50 after 15 years.
• • •
Missing some Tweet in this thread? You can try to
force a refresh
Article Guardian 'The mind/body revolution:' covers FND as the case example - Simon Wessely says its "unbelievably rare" - well his colleagues in UK psychiatry have actually pushed for it to be common based on their view that all medically unexplained symptoms in neurology departments may be called FND. theguardian.com/society/2025/j…
2. it will not be lost on all my followers that Prof Simon Wessely is a psychiatrist who pushed hard in the 1990s-2000s that illnesses such as ME/CFS and Fibromyalgia had no biomedical basis - essentially he and colleagues pushed a narrative of a biopsychosocial model without biology - and to have him be the commentator on the mind body revolution is ironic. If we look at depression research we see strides to show inflammation as a possible cause, changes in biochemistry following environmental factors, and genetics - thats true bio-psycho-social. But the same model has not been applied to ME/CFS and most likely is not being applied to FND.
3. You may notice the lack of mention in the Wessely narrative of viruses, or bacteria, or any pathogen as a possible trigger for any chronic illness, taking a healthy human into ME/CFS or other - the entire focus of germ theory medicine from 1800 to 1999 wiped away by a new view of "...emotional distress, environmental challenges, childhood trauma or “even being sedentary" as the important risk factors. We see pendulum swing, not a true integrative model, but a psycho-social swing, and whilst all factors are important, the key question is which are most salient to understanding cause and working out treatments.
I think this really shows a clear and dangerous dogma in health psychology, that the 4 conditions focused on in the trial, IBS, Fatigue (ME/CFS), Pain, Fibromyalgia, are not "explained" & this CBT-based training does not explain all medically unexplained symptoms conditions.
The authors challenge the legitimacy of the term medically unexplained symptoms, but in paper they promote the notion of an even more nebulous disorder concept, Somatic Symptom Disorder or Bodily Distress Disorder, and assert that 2/3rds of participants meet the criteria for SSD.
In the trial, the patients with so-called MUS are not clearly defined, we have no data on complaints they have, MUS is very loosely defined, the inclusion criteria is difficult to understand, and high MUS score patients are excluded as they have too much MUS!
@CGATist Prof Ponting is right to warn new researchers that ME research will not support careers, because it is almost impossible to stay focused on it long-term without funding. It is almost impossible to continue focusing on ME, so researchers move on.
I would like to raise the issue that UK ME charities tend to prioritise biomedical *lab research, meaning medico-health sciences research, epidemiology & the types of research myself and other health reserachers do, and want to do, is now severely restricted. So how to cotinue?
I wrote a letter titled "The Funding Gap" in ME to the 3 major ME charities in the UK. @MerukCEO @MEAssociation @actionformeI have recommended they collaborate to promote fellowships, PhD studentships, and long-term funding to keep people like me & others, focusing effort on ME.
Acu Seeds & the Power of Belief: I spent an hour listening to a podcast with the @BBCDragonsDen contestant/director of Acu Seeds about her healing journey with ME/CFS. In her own words she says she was diagnosed with Jan 2019, made a 60% recovery by June, and 100% by Feb 2020.
A few important points: 1. data shows that younger people who suffer post-viral fatigue, eg post EBV/Mono, have a 90% chance of recovery within 1 year, it is only around 10% that go on to have symptoms post 12 months. 2. Ascribing recovery to any one factor, is fraught with bias.
3. I celebrate this person getting their health back. 4. Belief is a powerful emotion. She says she saw a chinese herbalist who put her on 60 different herbs and treatments (I assume this is wordplay & not factual in numbers terms). 5. Ear seeds appear to have played no part imo
Just started listening to a couple of talks by the COFFI group, Collab Fatigue Following Infection - intro by director about choosing to get well after Long-Covid set the exoected psycho-behavioural control over illness tone, so far! coffi-collaborative.com/post/live-semi…
Watching these videos does make me feel a bit like a party pooper - for instance, I'd say to this speaker we "feel' tired after activity, we also "feel" tired after flu, whats the difference, explain the biology to me?
Each speaker deserves to be heard and with respect, but their ideas and models don't deserve respect, especially when outdated, here we have the Treat Response - HPA axis kick in - Fear-Avoidance Behav Model that is crude, it in no way explains ME or LongCovid - its small minded.
I want to share some feedback of trying to continue ME/CFS research: I am struggling to continue in ME/CFS work due lack of funding despite effort & this is a challenge I do not know how to fix on my own. So, I am sharing my experience with all ME advocates/charities/supporters.
- I have had the most amazing support over the past few years from the ME community, esp via crowdfunding drives, from charities and private donations, however it is a real struggle to keep going without consistent funding, and I have shared this issue with UK charities this year
- I have had to halt my ME/CFS work, until I find a way to fund projects. I have published many scientific papers on ME/CFS, but this year I have struggled to secure long-term funding support. I shall share a bit more on this. Applying for grants can take months of work.....