Thursday, September 18, 2014

When Medical Research Ethics Fall Short



A short while ago I was asked my opinion about a promising new treatment for depression being evaluated at a prominent research hospital.  I looked at the description on the hospital’s website, and it did indeed look interesting. I called the study coordinator for more details.

He told me the therapy involved adding energy to parts of the brain that might be involved in depression, and evaluating the results over a period of several months.  After my experience with TMS (which adds magnetic energy to the brain) I felt the idea sounded promising enough to be worth exploration.

Patients who enrolled in the study would go to the hospital twice a week for the duration of the study, which would be 2-3 months.  Then we got to the “fine print.” Half the participants would get the therapy, and half would get a placebo (a treatment that does nothing.)  Hearing that, I asked if the people in the placebo group would have the option to come back after the study sessions, and get the real treatment.

“No,” he said, “we don’t have funding for that.”  Wrong answer, I thought to myself.

When scientists construct a study that tests a new therapy for depressed people, they have an ethical duty to their subjects, and the structure of this study falls far short of what I’d find acceptable, as an ethical advisor.  I was surprised it made it past the hospital’s review board.  I was tempted to raise the question with them, but I didn’t.

If you’re testing a therapy that might help gifted kids read faster, this design might have been ethically ok, because volunteers in such a study would not be described as “suffering.”  People who enroll in a depression study are certainly suffering.  Asking a population that lives in pain to volunteer for research while withholding possible pain relief from half of them is morally wrong. Period.  There’s not much room for discussion about that, in my opinion.

We’ve gone down this road with autism pharmaceutical studies, where policies have evolved to the point where people who get a benefit from experimental medications can continue to take them after the study is complete.

Anyone who signs up for a study like this does so in hopes of gaining a benefit.  They don’t sign up to be “control patients” who get a sham treatment for purposes of comparison.  No one would knowingly do that.

“We thought they’d sign up to get the money,” the study coordinator told me in a weak voice.  Two hundred dollars for eighteen sessions, each of which takes 3-4 hours out of your day?  Let’s get real.  That’s two bucks an hour; an inducement that I found insulting at the suggestion.

“We had a really strong placebo response,” he told me, in a further effort to justify the flawed study design.  I’m aware of that effect, and it wasn’t surprising to hear him say that.  Basically, what he was saying was that patients who received a sham treatment reported almost as much benefits as patients who got the “real thing,” and the researchers wanted to separate people who truly got better from those who just imagined they were better.

That’s a real and valid concern in medical research where the power of positive thinking can make people think they are better even when they didn’t receive any medical value from a treatment.  We often see placebo responses that are similar to the real thing.  So how should researchers tell them apart?

One good way – in a psychiatric treatment like this – is to double the length of the study and give each subject both therapies. The subjects can be told they will be tested with two possible treatments, one of which is a placebo.  Half the group gets placebo first, half gets the actual treatment first.  Each group gets the other treatment after an appropriate “cooling off” period.  That way, the placebo effect can be compared in the same individuals.

The alternative would be to offer the actual therapy to the placebo patients after the study has run, and after announcing they were in the placebo group.  That would be ethically incorrect if it came as a surprise, but it would be OK if people were told they might be in a placebo group at the outset.

“Those are good ideas,” the coordinator told me, “But we didn’t have money to do what you suggest.”  How does one answer that?  Is it better to run an ethically flawed study in hopes of a strong result? Or is it better to hold off until an ethically sound study can be funded?  Now we have a different ethical question – one of benefiting the few versus benefiting the many.

The design of this study did not have the potential to harm participants directly but it could increase suffering for those who discovered they were in the placebo group.  It certainly subjects half the study participants to hardship for no real benefit.  Is it OK to do that to twenty people in hopes of developing a beneficial therapy for thousands?

I think the answer is no, when we place the study in context.  This is a well-funded research hospital, and when we consider the costs to save the twenty initial subjects from possible pain, that cost is trivial in the broader scheme of things.  The study should be properly designed and funded, or not done at all.  Getting funding is the researcher’s job.  You don’t save money at the expense of your subjects, unless there is no possible alternative, and a huge comparative benefit.

This study is not a “one or many” example where one person is sacrificed to avoid the sure death of a thousand.  That’s the stuff of action movies, not medical science.  This is considerably more pedestrian but still important to the patients who trudge to the hospital for three months, and get nothing for their depression but a thanks for helping science.

The final argument - That's the way we've always done these studies - is just disappointing.  Two hundred years ago, unsuspecting animals and sometimes people were dissected while alive, in the name of what was then legitimate science.  Ever hear of "Anti-vivisection societies?" That was what got them going.  Ethics evolve, and this is an example where evolution is called for today. 


As someone who has served on several medical research ethics boards I found it troubling that a major hospital would design a study with such obvious (to me, at least) ethical flaws.   What do you think?  Am I missing something here?

John Elder Robison is an autistic adult and advocate for people with neurological differences.  He's the author of Look Me in the Eye, Be Different, Raising Cubby, and the forthcoming Switched On. He serves on the Interagency Autism Coordinating Committee of the US Dept of Health and Human Services and many other autism-related boards. He's co-founder of the TCS Auto Program (A school for teens with developmental challenges) and he’s Neurodiversity Scholar in Residence at the College of William & Mary.  The opinions expressed here are his own.

8 comments:

David Smith said...

Sadly, much research is driven by the carrot of strictly budgeted allowances for such studies. In a "publish or perish" environment, the temptation is strong I think, to conduct a weak study simply for the researchers to remain employed. Hospitals look the other way, as each published study done in their name looks good to a board of directors. The question remains an open one in how to shift the incentive towards strong methodology and ethics. Even in cases like this, where the goal is laudable, an environment where funding has been drastically reduced from state and federal coffers creates it's own ethical problems within the system.

spdpd said...

John, you are spot on. Dave, in the previous coment says it well. In todays global pharmasutical market, it is a do or die racket. In this case, it would make better sense to reduce the number of subjects to be tested by at least half so all can benifit.

MountainMeg said...

I was in a study with TMS treatment for major clinical depression. The statement "The design of this study did not have the potential to harm participants directly but it could increase suffering for those who discovered they were in the placebo group." is, unfortunately, untrue.

In my experience, I had to stop taking an antidepressant (which wasn't working great) in a very short time - 6 days. That causes real, physical problems.

I never found out if I was in the placebo group, though I suspect it. I felt pretty good until 4 weeks after the study conclusion, at which point the depression came back harder and worse than ever. Wish I had never participated!

Car said...

Did the placebo group still receive the standard therapeutic treatment, or did they have no treatment at all? It would be extremely unethical if they withheld all treatment, especially proven standard therapies.

Did they have a way to monitor the psychological well-being of the patients? 2-3 months is a long time to be on a placebo, and depressive symptoms have the potential to cause great harm. I hope they are monitoring this risk and withdrawing volunteers who are suffering.

If they found the experimental treatment to be significantly effective during trials, would they stop the placebo group or would they have them complete the entire trial?

I also hope it was made very clear to participants that they could be in the placebo group and that people in the placebo group would not get the same benefit from the study.

keista said...

I think this is standard protocol. Because it's depression it should be handled differently than say, diabetes or high blood pressure? You are also assuming that the treatment WILL work, and will not have any negative side effects. Just because it was benign for you doesn't mean it will be benign for others. What if it turns out that this is the exact opposite treatment that people with depression should get?

Having said that, it sounds like the pay for this research was really low and they'd have a hard time getting candidates anyway.

John Elder Robison said...

Keista, I did not do the study so it didn't have any effect on me. And you are right that I don't *know* it won't have harmful effects, I am repeating their disclosure. Thanks for your thoughts.

Blaze1428 said...

I agree with you, John, that this is an ethically lacking plan especially for the suffering that goes on with depression. There is a lot of effort and time being put forth by the research subjects for only a 50% chance of being in the experimental group who get the treatment. I think your idea of getting a real treatment exposure after the study is complete is a good idea. They could also use another treatment modality for the control group, though that could be sticky to figure out the logistics. I would not participate in this study given those parameters. As a nurse, I also question the ethics of such a proposition. Good call.

Marilee G said...

Unfortunately we are all lab rats. Yes, there are many controlled research studies where people actually sign up. But due to this lack of funding many of the supposed blind and double blind studies are done by letting the public purchase the medication and use it, long before it's actually approved for what they take it for. A few years ago a fibromyalgia drug was sold as such when actually it had not received FDA approval for fibromyalgia, but had only received FDA approval for depression. Or maybe vice versa? The point is that when I read the news that it had barely been approved for an illness I knew friends had already been taking for over a year, I was livid. But what can one person do? We are all just lab rats and Guinea pigs. Why do you think we are seeing such a surge in lawsuits against drug manufacturers. Release of patents are being done in shorter times, less testing and more just using us to see what happens. It's sad, but we have to take more control of our own healthcare and not blindly follow the doctors and pill pushers. Your questions about the study were warranted. How they did the study, and the lack of funding to do it completely right is the researchers fault. They didn't ask for what they needed to do a complete study. And if they did and it was denied then they knowingly did an unethical study. Sad, very saddened.