Australia University will Study Effects of Xbox on Physical Activity in ME/CFS Patients

The University of South Australia has approval to begin the trial, “Active video gaming to increase physical activity in adults with Chronic Fatigue Syndrome/Myalgic Encephalomyelitis.” The study has no set research criteria, despite studies that show 2 out of 5 patients are misdiagnosed with CFS, and 7 out of 10 don’t meet ME guidelines in Australia. The study does not include patients who are unable to attend the university, which automatically excludes 25% of the target group.
Dr Katia Ferrar (physiotherapist) of the University of South Australia says that state organisations will be recruiting patients for them, but Bridges and Pathways refuted that, saying it isn’t part of their research collaborations.
ME/CFS Association of SA confirmed that they are in the trial’s Stakeholder Advisory group and are recruiting people via their website. The association was asked their opinion on this study not using any criteria (i.e. Fukuda or International Consensus Criteria) and asked why this booklet for GPs is on their website, when the first recommendation for management is to “gradually increase activity”? They replied that they will not be answering questions directly.
Those questions remain unanswered.
Since the trial registration was criticised last year in, “Why patients should not enroll in a clinical trial of video gaming treatment for chronic fatigue syndrome,” the word ‘pacing’ has been added to the study’s title.
The University of South Australia’s Dr Katia Ferrar (physiotherapist), Dr Ashleigh Smith and Dr Kade Davison are conducting the study.
Here are questions we put to the researchers about the study:
What research criteria are you using to select patients? 
Dr Ferrar: The inclusion criteria for the study stipulate participants will need to have been diagnosed with CFS by a medical specialist and they will be requested to report which criteria were used for their diagnosis. Diagnostic uncertainty is an issue that has surrounded CFS research for some time, and unfortunately there still does not seem to be any consensus agreement. The inclusion criteria were designed to take a pragmatic approach which would provide the opportunity for sub-group analyses at the end of the study to determine whether diagnostic criteria were related to intervention outcomes.
How are you recruiting patients?
Participant recruitment will be primarily via existing professional networks with the South Australian ME/CFS Society and Bridges and Pathways, a support network for people with CFS in Adelaide. Several rheumatologists who regularly manage CFS clients have also offered their support for recruitment.
The Stakeholder Advisory Group is comprised of two medical specialists, three representatives from patient organisations, two laypeople living with ME/CFS and the research team.
What is the total cost of your study?
The research proposal has been funded by the Mason Foundation for a total of $60,000. Additional in-kind funding from the University of South Australia also covers the chief investigators salaried time on the project and consumables etc.
What is the video game they will be playing?
It is interesting that you ask – as this took a lot of time and discussion with experts in the field of health-related active video gaming to decide. The console that will be used in the study will be the Xbox Kinect. The Kinect sensor will enable to participants to exercise from their chair (sitting) or standing, and has a very accurate level of motion capture. The games we will be providing will be a dance-based game called Kinect Dance Central and a sports game called Sports Rivals. These were chosen for pragmatic reasons, they are off-the-shelf easily available games, and after informal consultation with some adults of varying ages and genders with CFS, a preference to sporting and dance-type games was indicated.
How can you have a control group at 12 months if you are also using them for testing at 6 months?
The pilot study is designed so that there is a 6 months comparison of the intervention to control and after that time the waitlisted control group will then participate in the intervention for the final six months.  This design is somewhat unconventional but has been used in previous studies. The six month randomised controlled trial component 1) was deemed sufficient to determine any increases in physical activity given the likely nature of varying inter-individual progression rates in this population, 2) allows comparison to control which is essential to determine whether the intervention is actually the ‘thing’ making the change. The second six months of the study 1) allows observation of long term adherence to active video game playing in the 12 month continual intervention group, and 2) allows both groups to participate which we feel is an ethical consideration.
Do you believe you have the support of the ME and CFS community?
The responses and interactions during consultation and discussion with people managing CFS and representatives from support groups such as the SA ME/CFS Society and Bridges and Pathways have been positive and this is why they have agreed to assist with recruitment. I feel it is essential to develop such interventions with the input of the ‘consumer group’ and stakeholders.
Part of the project involves forming a Stakeholder Advisory Group which will include rheumatologists, exercise physiologists and the research team, but, more importantly, several people from the general public who are managing CFS and at least two representatives from the SA ME/CFS Society and Bridges and Pathways; all of whom will help finalise the finer points of the intervention before it commences. The Stakeholder Advisory Group is soon to convene to finalise details. I acknowledge that perhaps some members of the ME and CFS community may not agree with all components of the study design, and I welcome any discussions with them in order to improve the proposed project.
What is your view of the PACE trial, in the UK, which looked at graded exercise therapy?
As a physiotherapist and someone who has for a majority of my professional time, which continues as an academic clinical educator, treating clients using active management strategies, I do not feel GET to be an appropriate method to increase the physical activity levels of any person with a chronic condition. Unfortunately, the issues surrounding the PACE trial have clouded some people’s thoughts regarding the benefit of physical activity for people with chronic conditions such as people with CFS. This is potentially detrimental given the indisputable research surrounding the health benefits of physical activity. Having said that, is also equally important to prescribe any increases in physical activity appropriately, and, as such, the study we will conduct uses self-paced physical activity progression principles, allowing each participant to be in total control of their progression, just like they would be in everyday life.
Did the ethics committee have any questions about your study?
The role of Ethics Committees are to ensure the best practice in research design to protect the participants, the researchers and the wider community. As a result, ethics committees always have a very long list of questions regarding every study that is submitted for consideration. The UniSA ethics committee requested clarification about various aspects of the study, but was primarily concerned with the risk (to the participants) mitigation components of the study. The safety of the participants is my most important consideration when running this or any research study. The ethics committee were satisfied with the processes in place to reduce the potential risk to any participant involved. These include but are not limited to: mandatory general practitioner clearance to participate, low risk identified on a standardised exercise screening tool, and physical activity pacing counselling and support throughout the intervention provided by an accredited exercise physiologist.
What kind of waiver or agreement will participants sign? Will there be any warning of danger?
Ethical conduct of research requires that research participants be informed of all real or potential inconveniences and harms. The participants will be provided with a detailed Participant Information Sheet which outlines potential harms and benefits and will have the opportunity to ask questions of the research team and seek advice from their medical practitioners prior to enrolling. All participants also have the right and ability to withdraw from the study at any stage. All of these are standard practices that are required by the Ethics Committee.
Will the data be available after the study is complete?
It is anticipated the findings of the study will be presented at both a conference and published as a manuscript in an academic journal in order to disseminate the study results throughout the scientific community. We will also endeavour to have the findings publicised via local media so the general public can also be informed of the findings. In addition, it is planned the members of the Stakeholder Advisory Committee (i.e. Bridges and Pathways and SA ME/CFS Society) will assist with dissemination of findings via their networks.
What do you say to critics who would rather see the money going to biomedical research?
Part of the proposed project would be considered biomedical research. The secondary research question seeks to understand the link between allostatic load and physical activity levels in this population. The allostatic load is a proposed model of inflammation that is now thought to explain the development of many major chronic diseases such as coronary heart disease. It is hoped that the proposed study will take a small step to understand the inflammatory responses to exercise of people managing CFS, hence furthering our understanding of the disorder.
While it is important to undertake a range of research to better understand the aetiology of CFS and identify strategies that might be effective in prevention of the syndrome, which might be considered biomedical research, it is also important to evaluate management strategies to help those already suffering from the condition. This includes evaluating strategies to improve physical activity levels which will help maintain a better background level of health and may assist with increasing overall wellbeing.

Response from ME/CFS Australia (SA):

Peter Mitchell, Secretary, responded on behalf of the Management Committee:

We have no input into the design of the trial.
We are cognizant of the many faults in the PACE trial which claims, incorrectly, to demonstrate the value of GET for people with ME/CFS.  We are also aware of the survey indicating the harm experienced by patients who have attempted GET.
Our organisation is therefore, unequivocally, opposed to the practice of GET for patients with ME/CFS, and we would not lend our support to any study that had that intention.
The background and brief overview of this research was presented to the society at a seminar in February, at which it was evident that Dr Ferrar has a good understanding of ME/CFS and the dangers of GET. Also, it is our understanding that the University of South Australia will be convening a reference group for the study, and that the reference group will include well-informed patients as well as experienced clinicians who understand the nature of ME/CFS and the harm GET can cause.
The Society will, therefore, decide whether or not to endorse the study after the consultation with reference groups has concluded and we have received official notification that it has been funded and there is intent to proceed.

Response from Bridges and Pathways South Australia: 

South Australia’s Bridges and Pathways explained they limit their research partners and are focussed on the new biological markers that will guide treatments at the clinic.
Did you raise any objections about this study?
We did not know about it until it was on the [South Australian] ME/CFS Society’s website.
What is Bridges and Pathways position on graded exercise therapy?
B&P uses a biomedical model of ME/CFS and have a recognition that many people have mitochondrial (energy making) faults or immune system faults that can be increased with physical exercise and stress. These pathways can now be measured and identified using laboratory tests. We do not include graded exercise therapy as one of our recommended treatments.
Which clinical guidelines do you recommend?
We only use the 2014-2016 International ME/CFS Primer based on the Canadian Clinical criteria because we believe it most recommends the multi-system, multi-function genetic, neuroendocrine, functional, mitochondrial, multiple infection, faulty immune system and gut pathways. All these need to be managed through a systematic, patient-centred, problem solving, layered investigation process.

What would you say to anyone considering being part of the trial?
We cannot really comment, but we are very aware that many people cannot use computers or video type games because of the hypersensitivity.This study is not part of the South Australian ME/CFS Clinical and Research Collaboration. Included in our upcoming activities is a conference / workshop on some of the new researchers to update them on the patient-centred, biomedical approaches to the management of ME/CFS.
This article first appeared in ME Australia. Thank you to the people who provided comments and feedback.

4 thoughts on “Australia University will Study Effects of Xbox on Physical Activity in ME/CFS Patients”

  1. Barbara from Germany

    I was not able to imagine, that after the pace trial there could be something still more ridiculous and worse thant that.
    But now I see, yes, it can!
    Now someone has the idea to try if one could not cure patients with ME/ CFS by active video gaming. Aha. At an australian University.
    Finally finding a trick to bring those malingerers and lazybones to activity and show that- if they forget to pretend that they are sick they will see that, yes, of course they can be activ?!
    What else will “academic scientists” still find to mock patients with that severe Illness? I am shocked and horrified.

  2. This is a junior high science fair project.
    I don’t even trust the findings of Griffith’s “we found a marker that could be the result of any medical issue” research. Just wait until no one else can replicate their findings using ME/CFS CCC, ICC or even SEID criteria. But they will have a patent and sell tests at a premium and look, in our new research using this test, 50% of the people that test positive recover from GET/CBT (because they won’t have ME/CFS) and 70% of people that meet ME/CFS criteria don’t test positive. Oh well.

    1. Thank you for reading and commenting Janet.

      Yes, criteria is so important. Many people share your concerns about this trial. Hopefully by continuing to ask questions we can improve the quality of research. although it is especially disappointing that neither the researchers or the patient association recruiting for the trials would provide further details.

  3. they. can’t. be. serious. ?!
    this is almost as stupid as a woman on CFS-L years ago – looking for a link between ME/CFS and alien abduction experience. for. her. graduate. thesis.

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