cfq

Investigating the factors associated with meaningful improvement on the SF-36-PFS and exploring the appropriateness of this measure for young people with ME/CFS accessing an NHS specialist service: a prospective cohort study Daisy Gaunt; Amberly Brigden; Chris Metcalfe; Maria Loades; Esther...

https://www.tomwademd.net/chart-of-questionnaires-and-tools-that-may-be-useful-for-assessing-me-cfs-seid-symptoms/ contact details https://www.tomwademd.net/contact/

I have had a letter published in the Journal of the Royal Society of Medicine entitled ‘Measuring improvement and deterioration in myalgic encephalomyelitis/chronic fatigue syndrome: the pitfalls of the Chalder Fatigue Questionnaire’ You can read the letter here (see posts below if you are...

Systematic Review of Primary Outcome Measurements for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) in Randomized Controlled Trials https://www.mdpi.com/2077-0383/9/11/3463 eta:

https://www.mdpi.com/2227-9032/8/4/427 eta: (This article belongs to the Special Issue ME/CFS – the Severely and Very Severely Affected)

I plan to submit these comments to the current version of the Cochrane review next week (sorry I took me so long to write these down - long story). I thought it might be useful to post it here on S4ME first in case someone notices any mistakes so that I can still correct these before formally...

(Mods, do what you will with this.) This paper from 1998 is regularly cited in various papers as showing that the CFQ is a reliable measure for CFS research. But read beyond the abstract.......... https://www.sciencedirect.com/science/article/abs/pii/S0022399998000221 so they were...

Mod note: This discussion has been split from a thread in the members only area. Recently saw this on the Bristol Chronic Fatigue Syndrome/ME Service website (under Research)...