Testing a newly developed activity pacing framework for chronic pain/fatigue: a feasibility study, Antcliffe et al 2021

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Testing a newly developed activity pacing framework for chronic pain/fatigue: a feasibility study

Antcliffe et al 2021

BMJ Open

Abstract

Objectives
To test the feasibility of using a new activity pacing framework to standardise healthcare professionals’ instructions of pacing, and explore whether measures of activity pacing/symptoms detected changes following treatment.

Design
Single-arm, repeated measures study.

Setting
One National Health Service (NHS) Pain Service in Northern England, UK.

Participants
Adult patients with chronic pain/fatigue, including chronic low back pain, chronic widespread pain, fibromyalgia and chronic fatigue syndrome/myalgic encephalomyelitis.

Interventions
Six-week rehabilitation programme, standardised using the activity pacing framework.

Outcome measures
Feasibility was explored via patients’ recruitment/attrition rates, adherence and satisfaction, and healthcare professionals’ fidelity. Questionnaire data were collected from patients at the start and end of the programme (T1 and T2, respectively) and 3 months’ follow-up (T3). Questionnaires included measures of activity pacing, current/usual pain, physical/mental fatigue, depression, anxiety, self-efficacy, avoidance, physical/mental function and quality of life. Mean changes in activity pacing and symptoms between T1-T2, T2-T3 and T1-T3 were estimated.

Results
Of the 139 eligible patients, 107 patients consented (recruitment rate=77%); 65 patients completed T2 (T1-T2 attrition rate=39%), and 52 patients completed T3 (T1-T3 attrition rate=51%). At T2, patients’ satisfaction ratings averaged 9/10, and 89% attended ≥5 rehabilitation programme sessions. Activity pacing and all symptoms improved between T1 and T2, with smaller improvements maintained at T3.

Conclusion
The activity pacing framework was feasible to implement and patients’ ability to pace and manage their symptoms improved. Future work will employ a suitable comparison group and test the framework across wider settings to explore the effects of activity pacing in a randomised controlled trial.

https://bmjopen.bmj.com/content/11/12/e045398?rss=1
 
A rehabilitation program is not pacing by definition. Can we please stop pretending that some behavioural changes could plausibly and realistically lead to a recovery of function in the high-impact chronic illness that we call ME/CFS?
Words, as Humpty Dumpty said are all about who is master: WHO = Rehabilitation is defined as “a set of interventions designed to optimize functioning and reduce disability in individuals with health conditions in interaction with their environment”.
 
Can't we just give all the funding that goes to this junk directly to patient groups or something? These people are completely confused about everything and just wasting everyone's time with their crap. And it's not improving with time. If they can't understand that pacing is not a treatment and that it's the exact opposite of what rehabilitation is there's just no point to any of this.

Oh, sure, you developed a novel pacing framework. Good for you, you made this. Pfffft.

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This should not be allowed under the new NICE guideline. It's GET, with all the usual worst CBT features. Only 12 patients with CFS were included, and half of them dropped out. They must have been very mild cases to be able to participate in weekly 3.5 hour sessions.
 
Can't we just give all the funding that goes to this junk directly to patient groups or something?

@Snow Leopard made a similar suggestion some time ago --- yea, well healed, healthy, individuals being funded to do pointless (or worse) research --- why not just give the money to the patients?

I see they are still sticking to subjective outcome indicators (questionnaires). Published in the BMJ ----. Who funded this?
 
The wording could have been a bit more original?

newly developed (actually stale as week-old coffee)
activity pacing (ever-so-sweetly forced labour)
framework (minestrone)
for chronic pain/fatigue (whatever, who cares?)
a feasibility (post-pre-post hoc pragmatic even) study,...





 
Which is interesting given that BPSers are increasingly arguing for 'individualised treatment plans'.
That's why one major component is pushing the apps and virtual programs. Which completely removes the individualisation, and shows that "training" the therapists is essentially useless, a pamphlet is equivalent (to zero). But they argue for both anyway, and everything in-between. Even though the only point is cost-saving, and so the programmable stuff is what most will get.

They never really thought this through. It's arguing for boilerplate standardization that is also fully individualized, like a fully automated industrial process that produces hand-made bespoke artisan products, complete nonsense. The contradictions are irrelevant, doublethink takes care of that. It doesn't even matter that none of this scales, even for PACE they recognized that it would be impossible to deliver this in practice, even if it worked, the economics of this are ridiculous. None of this is supposed to make sense, it's astrology for physicians.
 
At the NICE roundtable one of the Royal College reps raised the issue that nobody did GET any more and that it was now individualised treatments that did not involve the bad things in official GET. A representative of a patient support group (a medical expert) pointed out that however much this might be the case patients are are still being expected to undergo incremental exercise and ending up feeling much worse. I concurred.

The therapists need to be on their best behaviour here. The NICE committee bent over backwards to allow that things may have changed and that therapists are now enlightened and want to discard unproven incremental exercise programmes designed to make people better.

This article shows that this is very far from universally the case. There is a total lack of insight in this paper into the reasons why GET was de-recommended and why it should have been.
 
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