Ten organisations call for PACE data release, AYME refuses

Ten organisations so far have joined ME/CFS patient Clark Ellis’s call to Queen Mary University of London (QMUL) to release data from the PACE trial but one group has refused.

In early February, Mr Ellis asked seven major UK ME/CFS charities to write to ask QMUL to abandon their tribunal appeal against the UK Information Commissioner’s decision that they should release the data to a patient who had requested it.
Six responded — the ME Association, Action for ME, ME Research UK, Invest in ME, the Tymes Trust and the 25% ME Group. In addition, Hope 4 ME & Fibro NI, the Welsh Association of ME & CFS Support, the Irish ME Trust and Dutch organisation Groep ME Den Haag have joined them.
However, one group that he contacted — the Association of Young People with ME (AYME) — has refused to join the call. Mr Ellis said that the move “flies in the face of patients’ interests”.
AYME made their decision at a board meeting on 3 March but have made no public announcement. They emailed Mr Ellis, saying, “The QMUL data has already been released to and reanalysed by the Cochrane Collaboration (perhaps the most rigorous of research teams), which came to the same conclusion as the original researchers.”
AYME’s statement appears to indicate some confusion about the nature of the Cochrane Collaboration, which describes itself as an “independent network” of researchers and others, who can set up teams following Cochrane’s guidelines. The team who received the individual patient data from the PACE trial included all three of PACE’s principal investigators — Professors Peter White, Michael Sharpe, and Trudie Chalder. One of the team’s meetings was funded by Professor White’s academic fund. The results of their reanalysis have not been published.
In their email to Clark Ellis, AYME also stated, “This release to a bona fide researcher who has an ethical duty of care for the data complies with a condition of Medical Research Council (MRC) funding. For the same reasons, it remains open to other bona fide researchers to request the data, subject to the same ethical undertakings. Therefore there is no requirement for AYME to write to QMUL and we will not be doing so… No further comment will be made regarding our position on this matter.”
However, independent scientists who have requested the anonymised raw data have been refused by QMUL. They include geneticist Professor Ron Davis of Stanford University, biostatistician Professor Bruce Levin of Columbia University and psychologist Professor James Coyne of Pennsylvania University.
AYME’s lead medical advisor is Dr Esther Crawley, who is principal investigator for the MAGENTA study of graded exercise therapy for young people, dubbed “PACE for children” by the Welsh Association of ME & CFS Support. She has described PACE as “well conducted”.
Dr Crawley was also principal investigator on the controversial SMILE trial of the Lightning Process for children with ME/CFS. The Lightning Process is described by Phil Parker, its inventor, as a programme of “gentle movement” and “mental exercises” but has been dismissed by psychologist Professor James Coyne as “quackery justified by pseudoscience”. While other charities objected to plans for the study and called it “unethical”, its protocol was developed with the “active participation” of AYME.
Clark Ellis said, “I’m disappointed to see an ME/CFS charity letting patients down in this way. All the rest have been fantastic. I think it’s important to look at why AYME are acting differently from everyone else.”
He encourages patients outside the UK to contact their own national organisations and ask them to write to QMUL.

Facebook
Twitter
WhatsApp
Email

3 thoughts on “Ten organisations call for PACE data release, AYME refuses”

  1. jess marotta -porter

    why the secrecy? what are they hiding, if its medical records all should be pretty straightforwaord and okey dokey? Was there some patient neglect and or abuse thats being hidden. Its time to air out the cobwebs and release all those dead skeletons from the closet. The truth about scecrecy regarding this illness and the poor treatment of patients WILL eventually come out. Its time to admit mistakes, make apologies and move forward with honest science, not shady shenagans. There should NEVER be hidden or unaccessible records where children are concerned. right is right and wrong is wrong.

  2. Wendy Boutilier

    Canada also sent 2. But for some reason have not been included
    National ME FM Action Network
    Letter to the Lancet was sent on Feb 13th, 2016
    CIND Canada
    Non Profit ME Organization awaiting Charity Registration #
    Letter to the Lancet sent Feb 13th, 2016

Comments are closed.

Latest News

a dark plum square image with a brownish/purple square in the middle. The #MEAction logo is at the top center. the words: black ME voices: q&a with Teona Studemire are in a fancy white font. Black history month is at the bottom of the square surrounded by two black stars.

 Black ME Voices: Q&A with Teona Studemire

With it being Black History Month, it was crucial to me to make sure we spotlighted someone from the ME/CFS and Long COVID community who is Black. Being Black and disabled is an entirely different experience. Not only do we deal with ableism, but we also deal with racism, especially medical racism. According to the

Read More »
blue rectangle image with the NIH logo in the top left hand corner. the words: NIH MECFS Research Roadmap Update Public comments open until March 8th appear in the middle of the image. the meaction logo is in the bottom right hand corner.

NIH ME/CFS Research Roadmap Update–Public Comment Period Now Open

The NIH ME/CFS Research Roadmap public comment period is open now with a deadline of March 8th.  #MEAction is a member of the ME/CFS Research Roadmap Working Group and for the past several months we have been advocating on behalf of this community within this group. Our Executive Director, Laurie Jones, served on the nervous

Read More »
Scroll to Top