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UK: Workshop - CBTReach - CBT for Persistent Physical Symptoms, Chalder - 9 May 2023

Discussion in 'Other psychosomatic news and research' started by Sly Saint, Jan 11, 2023.

  1. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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    ABSTRACT
    Cognitive behaviour therapy for persistent physical symptoms: what to do and how it works?

    Professor Trudie Chalder


    Overlapping, common, persistent physical symptoms, not associated with significant pathology, are associated with profound distress, sleep disturbance and disability. Patients with these symptoms attract a range of different labels including irritable bowel syndrome, , chronic fatigue, cough hypersensitivity, fibromyalgia, and dissociative seizures. Around 50% of patients in secondary care have symptoms such as these. Evidence has accumulated for the efficacy of cognitive behaviour therapy. Some studies focus on one syndrome such as irritable bowel syndrome while others take a transdiagnostic approach.


    The aim of the workshop is to,

    (1) describe specific and transdiagnostic models and treatment approaches for persistent physical symptoms, and

    (2) describe evidence of efficacy and mechanisms of change.


    This workshop will be useful for qualified cognitive behaviour therapists and clinical psychologists working in primary or secondary care, occupational therapists, psychiatrists, and primary care physicians.


    In this workshop you will develop an understanding of why physical symptoms persist within a cognitive behavioural framework, the extent to which they can be changed and how they can be changed. Building on your existing skills you will expand your repertoire of skills and techniques that will translate into effective change for your clients and patients. A range of self-report scales will be described as well as self help materials for patients.



    References


    Chalder T, Willis C. ‘Lumping’ and ‘splitting’ medically unexplained symptoms: is there a role for a transdiagnostic approach? J Ment Health. 2017 Jun;26(3):187–191. doi.org/10.1080/09638237.2017.1322187


    Chalder T, Patel M, Hotopf M, Moss-Morris R, Ashworth M, Watts K, David AS, McCrone P, Husain M, Garrood T, James K, Landau S. Efficacy of therapist delivered transdiagnostic CBT for patients with persistent physical symptoms in secondary care: a randomised control trial. Psychol Med. 2021 May 31. doi.org/10.1017/S0033291721001793 [Epub]


    Husain M, Chalder T. Medically unexplained symptoms: assessment and management. Clin Med (Lond). 2021 Jan;21(1):13-18. doi.org/10.7861/clinmed.2020-0947


    Windgassen S, Moss-Morris R, Goldsmith K, Chilcot J, Sibelli A, Chalder T. The journey between brain and gut: a systematic review of psychological mechanisms of treatment effect in irritable bowel syndrome. Br J Health Psychol. 2017 Nov;22(4):701–736. doi.org/10.1111/bjhp.12250


    https://www.cbtreach.org/about
     
    Ipquise, Louie41, Hutan and 4 others like this.
  2. Sean

    Sean Moderator Staff Member

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    Yet. And never will be if you don't look for any. Which you never have.
    Not chronic fatigue syndrome?

    Increasingly slippery games with words won't save you and your empire.
     
    bobbler, RedFox, Ash and 15 others like this.
  3. Charles B.

    Charles B. Senior Member (Voting Rights)

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    Using the terminology “chronic fatigue” seems so disingenuous. Can anybody attest to Chalder’s reputation amongst physicians and academics? It seems she’s highly regarded, and it’s utterly bewildering why.
     
  4. duncan

    duncan Senior Member (Voting Rights)

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    Interesting choice of references (reference material) for the workshop. :)
     
  5. bobbler

    bobbler Senior Member (Voting Rights)

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    She cares so much about the people this treats it is now 'transdiagnostic'? - 'let's not diagnose anymore because it only wastes my time listening to what you think you have when the treatment will be the same anyway'. Just so happens that without having to diagnose any condition I can sell my cure based on my own personal form selling merely 'they'll fill this form out differently at the end'.

    "What did they have?".... "lower scores on average for my forms than before they did the session" .... "oh, so what shall we fund it under.. low/high score syndrome?" should surely be the discussion? How is this getting away with 'all diseases' instead of 'no illnesses' it has been proven to work for being the assumption of this?

    That 'should people be allowed to do useless bad research' thread is really important here. Morally obviously not, as well as many other obvious reasons. They do it for many reasons and the impacts.....


    operationalising the 'it's in yer head just try focusing on not doing ill and distracting yourself to not focus on it' bigotry to pretend it's 'science' based on the fallacy 'really bad, biased research set-up merely as a vehicle to carry your opinion-based narrative and fait-a-compli claims is better than the 'no research' you claim is the alternative - when even if that were the case basic logic, decency and respectful clinical approach would surely be that?
     
    Last edited: Jan 11, 2023
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  6. Trish

    Trish Moderator Staff Member

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    It appears to be quite easy to be highly regarded if you stay within your clique of like minded people, produce masses of publications and get lots of research funding. Professorships will ensue.
    Regardless of research quality, signs of intelligence, or ethical integrity. Just keep churning out the same old garbage.
     
  7. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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    I can't find the link to it but on one of the various sites (might be one of the FND ones where she is a medical advisor) it says that TC was the first Professor of CBT.
     
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  8. Adrian

    Adrian Administrator Staff Member

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    Clearly CBT is a universal cure for everything so why have diagnosis. Just convince a patient there is nothing wrong with them and that they can go away and disapear and hence be judged cured.
     
  9. Trish

    Trish Moderator Staff Member

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    Clearly CBT is not going to cure anything, and the perpetrators of this con seem to believe that a minor uptick on a questionnaire outcome for some patients is sufficient to justify it. And clearly it's mainly offered as a way of getting bothersome patients out of the hair of doctors and into the hands of lower paid CBT practitioners.

    But what I think needs to be shouted loud and clear is this:

    Not only is CBT not effective in any long term or meaningful way for many patients - it also CAUSES HARM, as I know to my cost.
     
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  10. Adrian

    Adrian Administrator Staff Member

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    And do we need to list the ways it causes harm?
     
  11. CRG

    CRG Senior Member (Voting Rights)

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    It's on the page you linked to :): https://www.cbtreach.org/about - next to her oversized photo

    Trudie Chalder PhD

    Professor of Cognitive Behaviour Therapy

    Department of Psychological Medicine

    IOPPN

    Kings College

    University of London.

    Trudie is the first Professor of CBT in the UK and President of BABCP 2012-2014
     
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  12. Trish

    Trish Moderator Staff Member

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    I think a study of people who have found CBT unhelpful could be quite enlightening for CBT therapists to read.

    In my case the CBT was prescribed to help me cope with distress following losing my career because of ME/CFS. The negative effects included gaslighting (acting as if my physical symptoms and disability didn't exist, eg making no accessiblity adjustments), not acknowledging that I needed time to grieve, and leaving me feeling more of a failure. The focus on trying to persuade me that my negative thoughts were wrong thoughts was harmful.
     
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  13. John Mac

    John Mac Senior Member (Voting Rights)

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    Yes very strange that your only references are your own studies!
     
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  14. Peter Trewhitt

    Peter Trewhitt Senior Member (Voting Rights)

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    There was the survey done at the request of NICE early on in the ME/CFS guidelines rewrite process, that asked both about GET and CBT, though I can’t remember where it was published and whether it had any detail.
     
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  15. Adrian

    Adrian Administrator Staff Member

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    I think Trish covered some of the reasons CBT can be bad. But there are others such as someone is put off going to the doctor and other (acute) diagnoses are not explored. Or that someone with ME does too much and becomes more severe.

    I think it is useful to think through the different possible consequences in understanding safety as they you can look at the data with a finer grained analysis
     
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  16. bobbler

    bobbler Senior Member (Voting Rights)

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    I fully agree that the harm caused by this dodgy ‘CBT’ needs to start being unbundled and defined. Like that everybody’s welcome (is that the right name?) page.

    too many who shove others off into it believe they brochure ‘it will help people cope’ and think they don’t need to interrogate if that’s nonsense, about what, and won’t open their mind to the idea it can be psychologically and physically harmful as a treatment.

    one reason I suspect is simply because of the tendency for certain individuals to throw ‘anti mental health’ at anyone who rightly - as they should for anyone led overall safety - asks whether something has risks and could actually be harmful even if it is technically under ‘psychological retraining’ because after all that term doesn’t include only things that retrain in ways that are helpful and don’t harm.

    So it needs blatant defined harm to stop them suggesting they are the victim of someone saying their treatment is bad by spelling out they aren’t, the ones it hurt - in this way - are the ones who can be heard, tell their story and not be accused of anything other than reporting safety info.

    I think cfs-CBT is perhaps worse than GET as it’s more persistent in its gaslighting residue lurking for years, it’s those courses that deliberately stay up online to influence support networks to not support disabled people (goodness knows what it does to many relationships), and it’s tentacled into the practice of physios, OTs, nurses

    the worry is it’s been trained as if it’s a good technique without them realising it’s just bullying invalidationand lack of empathy under a pretence of ‘therapeutic technique’ when you step back - and that these are fundamentally terrible things in any profession but really bad in medicine and where there is a power imbalance. And that the ‘embedded stuff’ won’t get unpicked like the courses might unless someone spells it out as a wake up call.

    how do we get this dirty underbelly out from ‘embedding’ everything without blowing up the myth that ‘bad is good’ [as long as you claim good intentions with no proof you put much effort into checking those intentions matched consequences of said actions] and saying no it’s just bad and look what it actually does on the ground when it infiltrates access to everything service or support wise …. Without holding up a mirror to the consequences of what it does?
     
    Last edited: Jan 13, 2023
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  17. Ipquise

    Ipquise Established Member (Voting Rights)

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    There have also been cases where cognitive behavioral therapy has been a cure. I would not write off this type of treatment. Let it evolve like all other therapies.
    In general, the topic of psychosomatics is very interesting. People like to make things up :) They can even make up a disease for themselves :) Quite real ones! And they can do it both consciously and unconsciously.
     
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  18. Hutan

    Hutan Moderator Staff Member

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    It depends on the underlying paradigm of the therapist. It can be harmful when the therapist believes, with no good evidence, that the patient isn't really sick, and just needs to think more positively.

    If you are ill and get told it is all in your head, and yet the psychological treatments for the supposed imaginary illness don't work, that is a problem. You are still sick, but also feel disbelieved and/or inadequate for not being able to recover.

    Psychosomaticism has often been used as a way to label illnesses where the doctors don't know what is going on; they don't need to feel bad about their ignorance, or do anything constructive about it, but can instead blame the patient for thinking incorrectly. @ME/CFS Skeptic has a great blog series about this - see this thread
    ME/CFS SKeptic: A new blog series on the dark history of psychosomatic medicine

    If you believe that you have some evidence for psychosomaticism, you might like to start a thread to chat about it. I'm sure people will join in the conversation :).
     
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  19. Charles B.

    Charles B. Senior Member (Voting Rights)

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    There is an evidentiary double standard in psychosomatic land though. Those suggesting these post-infectious conditions are driven by organic pathological processes are required to produce consistent, replicated, and objective anomalies that could explain clinical presentations.

    Psychosomatics traffic in the amorphous. I think your line, “people like to make things up,” perfectly illustrates this point. As far as CBT, the issue is perpetual underperformance in clinical trials. There are anecdotes supporting an eclectic array of interventions for the constellation of symptoms falling under the auspices of CFS. That doesn’t make them universally applicable.
     
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  20. Trish

    Trish Moderator Staff Member

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    I'm not writing off CBT completely. I accept that there may be people who find it helpful for making changes they want to make in the way they handle some issues in their lives, perhaps related to how they cope with anxiety or phobias. Though I suspect really successful interventions depend more on a wise and empathic counsellor/therapist working to the patient's agenda, rather than a therapist applying a preset process according to what they believe is best for the patient.

    What is being offered in CBT for persistent physical symptoms is something different from CBT for anxiety/phobias etc.

    It is a directive form of CBT that endeavours to persuade the patient that their symptoms are psychogenic, and that they need to learn to ignore them and push through and try to function normally and with positive thoughts about their health, to overcome what the therapist has been taught is the patient's abnormal fear of exercise, etc.

    There is no credible evidence I have seen anywhere that thousands of people are imagining themselves sick or making things up. That sounds like prejudice to me, not medically established fact. Are you really suggesting that the millions of people around the world with ME/CFS, fibromyalgia, Long Covid etc are all imagining they are sick?

    If so, how come CBT hasn't worked in clinical trials?
     
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