From the protocol: http://www.biomedcentral.com/1471-2377/7/6
Previous research has found that people with ME/CFS report higher Borg scores when doing exercise tests. I'm rusty now but I think one or more from the CBT/GET school proponents have commented on this. I think they may have expected an improvement from GET and probably CBT. The latest paper talks about tolerance to activity as being the 6-minute walking test. One could argue another measure for this is the Borg scores (which measure perceived exertion - they adjust them by dividing by % of predicted maximum heart rate reached).
There was little talk that there was no improvement for the Borg score (at 12 weeks anyway).Process of treatment
We do not know the mechanisms of successful treatment for CFS/ME. Do illness beliefs or focusing of attention on symptoms (symptom focusing) need to be changed for CBT to be effective? Or do CBT and GET both work by improving tolerance to activity? Is increased physical fitness essential to recovery or not? How important is the alliance between therapist and patient? Is it necessary to adapt to the limitations imposed by the illness to reduce fatigue? A greater understanding of these processes will shed light on the essence of improvement and allow the development of more efficient treatments.
Previous research has found that people with ME/CFS report higher Borg scores when doing exercise tests. I'm rusty now but I think one or more from the CBT/GET school proponents have commented on this. I think they may have expected an improvement from GET and probably CBT. The latest paper talks about tolerance to activity as being the 6-minute walking test. One could argue another measure for this is the Borg scores (which measure perceived exertion - they adjust them by dividing by % of predicted maximum heart rate reached).