Opinion Is the RACGP HANDI recommendation of incremental physical activity for CFS/ME harming patients?, 2026, Stallard/Praet/Gupta/Smith

Dolphin

Senior Member (Voting Rights)
AJGP > March > Is the RACGP HANDI recommendation of incremental physical activity for chronic fatigue syndrome

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Volume 55, Issue 3, March 2026

Is the RACGP HANDI recommendation of incremental physical activity for chronic fatigue syndrome/myalgic encephalomyelitis harming patients?​

Jacqueline Stallard Stephan Praet Sandeep Gupta Angela Smith

doi: 10.31128/AJGP-03-25-7614 | Download article

In April 2024, The Royal Australian College of General Practitioners (RACGP) Handbook of Non-Drug Interventions (HANDI)committee published a guideline: Incremental physical activity for chronic fatigue syndrome/myalgic encephalomyelitis.1 The HANDI committee claims to recommend interventions that are based on ‘solid evidence’.2 But is this always the case?

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Thinks PACE and Larun’s exercise review were good, but says that surveys about harm are at a high risk of bias so we don’t care about those.
The 2023 NICE guideline retraction was highly controversial and not aligned with research evidence, resulting in members of its writing group resigning. Details of the aberrant interpretation of evidence are outlined elsewhere.5,6
The attention to detail is worrying. It was 2021, and it wasn’t a retraction - it was an update.
 
Are there published data that show that GET is harmful?

I know that there are patient surveys that show this clearly. Are those the best evidence?

Is there any better evidence to point to?

(There probably is a specific thread about this somewhere.)
 
Are there published data that show that GET is harmful?

I know that there are patient surveys that show this clearly. Are those the best evidence?

Is there any better evidence to point to?

(There probably is a specific thread about this somewhere.)
The PACE trial data? NICE ng206 wrote about it.
 
Are there published data that show that GET is harmful?

Maybe the important thing is that there is no evidence showing it's helpful.

Any treatment not supported by evidence might be described as harmful, and is certainly unethical. Even if it didn't make people more ill, it's still a waste of taxpayers' money and patients' and clinicians' time.
 
Yes, “some patient groups” raise methodological critiques about GET trials and not the rest of the field that a clique have siloed themselves away from by intentionally using alternative nomenclature. Definitely not.

Top kek.
 
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