2014
DOI: 10.1136/eb-2014-101961
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Response to: reports of recovery in chronic fatigue syndrome may present less than meets the eye

Abstract: Friedberg and Adamowicz 1 make several interesting observations in their review of recovery rates reported in White et al. 2 However, we disagree with them that a previous trial of an active behavioural intervention, Deale et al, which reported very similar recovery rates to White et al, 'used similar recovery criteria'. [1][2][3] The White et al 2 recovery criteria were: Chalder Fatigue Questionnaire (CFQ; Likert scoring) and Short Form (SF)-36 physical functioning (PF) scores in normal range (ie, ≤18 and ≥60… Show more

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Cited by 2 publications
(2 citation statements)
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“…An analysis of the PACE trial suggested cure was possible, but recovery outcomes were defined post hoc using population norms with generous thresholds (such as the population mean plus one standard deviation for self reported fatigue). 15 This analysis was criticised because of the limited assessments and less than full restoration of health, 16 leading to a recommendation that trials use more accurate outcomes (such as clinically relevant improvement) defined in advance and capturing a broad based return to health with assessments of fatigue and function.…”
Section: Prospects For Curementioning
confidence: 99%
“…An analysis of the PACE trial suggested cure was possible, but recovery outcomes were defined post hoc using population norms with generous thresholds (such as the population mean plus one standard deviation for self reported fatigue). 15 This analysis was criticised because of the limited assessments and less than full restoration of health, 16 leading to a recommendation that trials use more accurate outcomes (such as clinically relevant improvement) defined in advance and capturing a broad based return to health with assessments of fatigue and function.…”
Section: Prospects For Curementioning
confidence: 99%
“…Prior to publication of the PACE trial results, a small number of clinical trials had supported the use of CBT and GET, almost all of which had been carried out by health professionals who promoted a psychosomatic model of causation and management. However, patient survey evidence, as collected by the ME Association (ME Association, 2015) along with most other patient surveys (Kindlon and Baldwin, 2015), told a very different story. The majority of people with ME/CFS consistently reported that CBT was ineffective.…”
mentioning
confidence: 99%