https://www.mahanatx.com/treatments/ibd-researchA New Way to Treat IBD
Mahana is currently developing a personalized digital treatment for adolescents and adults with Inflammatory Bowel Disease. This product will be tested in a series of research studies and randomized, controlled trials. This treatment will tap into the power of Cognitive Behavioral Therapy (CBT) to help patients living with IBD.
Is this venture capitalist unable to assess claims of treatment efficacy and a little gullible or does he not care whether it really works or not?
http://www.virology.ws/2020/02/17/trial-by-error-my-follow-up-letter-to-mahana-therapeutics-ceo/Last week, I wrote to Rob Paull, the co-founder and CEO of Mahana Therapeutics, regarding the company’s misleading claims about the web-based cognitive behavior therapy program for irritable bowel syndrome it recently licensed from King’s College London. I have also written to Professor Rona Moss-Morris, the co-lead investigator of ACTIB, the study that road-tested the program, as well as three of Mahana’s prominent gastroenterology advisors.
So far, no one has responded or attempted to explain why Mahana is making unwarranted statements about the efficacy of the program. Presumably the company would like to have regulators in the UK and the US approve the product for public use. If so, it would be smart for Mahana and Mr Paull to be honest in describing what the findings do and do not show. So far, they have failed that test.
https://www.berkeleywellness.com/healthy-mind/stress/article/cbt-ibs-worth-tryIrritable bowel syndrome (IBS) is a common gastrointestinal condition characterized by cramping, bloating, gas, and diarrhea or constipation. It likely has multiple causes, and many patients continue to suffer despite taking medication. Cognitive behavioral therapy (CBT) has sometimes been recommended as a treatment based on the notion that it can help patients reduce stress, change their eating patterns, and modify how they think about the illness. But now the largest study to date of CBT for IBS has shown that it has little impact in reducing symptom severity.
The UK study, conducted by investigators at King's College London and the University of Southampton, included 558 people with unresolved IBS. Participants were randomly assigned to receive telephone-delivered CBT, web-based CBT, or no intervention. All three groups continued to receive their usual medical treatment. The study did not test in-person CBT. The 12-month and 24-month results were published in 2019 in, respectively, the journals Gut and Lancet Gastroenterology & Hepatology.
Short version: It is all your fault if you don't get better.
I think they originally wanted "Muhaha" but it was already taken by this guy:None of the Founders are Hawaiian or Maori either, so it still seems like cultural appropriation...
I hope the end result is the company collapses.
I can see the point of @dave30th pursuing this, even though his funding is for ME/CFS, not IBS. Rona Moss-Morris is heavily involved in doing the same sort of crap research and treatment for ME/CFS, and undoubtedly she and her colleague Trudie Chalder have plans in place to set up a similar company to sell their crap on-line CBT for ME/CFS as well, which I'm sure would be taken up with enthusiasm by the NHS.
If this IBS venture can be stopped in its tracks before it fully launches, not only will it help patients with IBS, there should be a knock on effect for patients with ME/CFS too - I hope.
I have been trying to find out why Mahana Therapeutics, a San Francisco-based start-up, has chosen to disseminate misleading information about a web-based cognitive behavior therapy program for people with irritable bowel syndrome. Because Mahana’s co-founder and CEO, Rob Paull, has not responded to my letters, I have contacted some of those listed as science advisors on the company’s website.
Earlier this month, I sent one such letter to Dr Mel Heyman, a pediatric gastroenterologist at University of California, San Francisco–one of Berkeley’s sister UC campuses. I received an automatic e-mail response that Dr Heyman was out of the office for a period of time. Last week, after his stated return date, I sent another letter:
Last week, BerkeleyWellness.com published a short article about the UK study at the root of the inflated claims that CBT is an effective treatment for IBS symptoms. The piece was blunt about the limitations of the findings. Here is the text:
Trial By Error: A Non-COVID Post about KCL’s Rejection of My FOI Request - https://www.virology.ws/2020/04/07/...-post-about-kcls-rejection-of-my-foi-request/
Profiting from pain
So it's official. UK universities put financial gain before academic integrity. I am disgusted.
Sadly no....but are you surprised?
The issues are over misleading scientific claims, hence the need for information. A deflection over commercial interests is as meaningless as saying "you can't investigate possible wrongdoing since I'm making money from it and that would be prejudicial to my self-interest". They are making medical claims aimed at dispensing clinical advice, this isn't a simple matter of protecting business and it's an academic institution anyway, different requirements. This ain't a corner rub-and-tug where you can hide something in a back room.
It's an interesting notion, albeit ethically bankrupt, that you can't question misleading science if it aims to be commercialized. Even though of course commercializing misleading medical advice is obviously highly problematic. Now that's a gigantic loophole if I've ever seen one.
Because this is kind of similar to LP and generally the CBT/GET paradigm. The evidence simply isn't there, even though some misrepresentation of it was published in medical journals. But it's a commercial product, therefore not subject to the public interest since obviously more information would unravel the business. This is borderline mob level of skirting legal obligations while appearing to adhere to thanks to protection from secrecy.
Great example of evidence laundering. The findings in the papers are weak. The public claims have nothing to do with the findings, they present it as outlandishly more effective than it actually is (familiar territory, lots of experience). Those claims have "commercial interest" and become not subject to scientific scrutiny. They are lying about their own research. But the research itself is weak and muddied, so is unlikely to be retracted as it makes very weak claims. It's the misleading amplification of those claims that becomes a commercial product, by exaggerating baseless claims but now this is outside of the scientific process so it's not subject to the usual requirements and anyway it's a self-help thingy so has nothing to do with medicine, therefore exempt from stringent clinical requirements.
This is genuinely villainous. It's the same moral bankruptcy we are familiar with so not surprising but this is completely outside of the purpose of scientific research, medical research and, especially, academic institutions. And the refusal here is one of those obvious cases of having lots to hide.
Put a few bad apples in a bunch. Wait a few year and even the barrel falls apart.
Sorry, I can't help. My involvement with the ME world doesn't extend beyond this forum.
Nope, sorry, my MP is a Minister in the government so wouldn't take an active part anyway, and I've never had the time, energy or inclination to attempt to interest him in engaging with the whole ME issue.
Nope, sorry, my MP is a Minister in the government so wouldn't take an active part anyway, and I've never had the time, energy or inclination to attempt to interest him in engaging with the whole ME issue.