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Application of normalisation process theory in understanding implementation processes in primary care settings in the UK: a systematic review - 2020

Discussion in 'PsychoSocial ME/CFS Research' started by Sly Saint, Mar 17, 2020.

  1. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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    https://bmcfampract.biomedcentral.c...mpaign=BSCN_2_DD01_CN_bmcso_article_paid_XMOL
     
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  2. alktipping

    alktipping Senior Member (Voting Rights)

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    a fancy way to write about protocols new language doesn't change the fact that most if not all healthcare industry protocols are not actually based on addressing patients needs and have everything to do with costs . another paper written just so the authors can claim to have published .
     
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  3. Invisible Woman

    Invisible Woman Senior Member (Voting Rights)

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    Wow. It took me a couple of goes to get my head around the title.

    Words for the sake of words.

    I can't be bothered.

    I'll wait till a few more reviews have been done and then read the meta analysis on that thanks.
     
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  4. MEMarge

    MEMarge Senior Member (Voting Rights)

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    This is so waffly/full of sociology blurb but the following sentence under the sub-heading "use and adaptation of NPT" (a couple of paras up from Table 5) made me want to shout out an expletive or 3.

    "However, one paper suggests that focussing on the individual and collective agency of actors who are delivering the intervention risk neglecting the agency of those who receive the intervention – particularly at a patient or service user level [44]."

    Also, under the heading:

    "NPT as a facilitator of understanding" - ( just under Table 5 in Results section.)

    "For example, Bayliss et al. reported that NPT revealed that owing to a large number of barriers the CFS/ME intervention was not feasible, and concluded that “time pressures and competing priorities meant that some GPs failed to engage with the training module (cognitive participation). When the module was completed, many GPs stated that it was not feasible to retain even the key messages as they saw so few patients with the condition” [32]."

    32.

    Bayliss K, Riste L, Band R, Peters S, Wearden A, Lovell K, et al. Implementing resources to support the diagnosis and management of chronic fatigue syndrome/Myalgic encephalomyelitis (CFS/ME) in primary care: a qualitative study. BMC Fam Pract. 2016;17(1):66.

    (The above paper is not a recommendation - numerous comments by GPs ....)

     
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