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I also think that this is a good idea. If there is any way that could possibly improve the health care system, then we should go for it. If this research could possibly reduce medical costs, then more people may be willing to seek medical help when they get sick or hurt. If someone cuts his hand, and he needs to go to the emergency room, he will may be more likely not to go if he knows that it is going to cost him a fortune to go. Even though this plan may decrease medical costs, it doesn't mean that it will reduce the profits that the company has. If more people will be willing to go to the doctors, the office will be bringing additional revenue and possibly even repeat customers. One of the biggest costs for businesses is trying to gain new customers. It is cheaper for a business to keep previous customers. I think that this program will increase the demand for medical assistance.
The article also states that this could maybe improve a person's quality of living. This would be kind of like an economic cost because it isn't something that can be valued in terms of money. The extra time that a patient is feeling better can't be valued with money. It will also make patients feel better because they will feel as if they know what is going on.
Mr. Kling: If your father is truly in the control group, then this study is badly designed. In a study comparing a new intervention to existing care, the patients randomized to receive existing care should be told nothing. This study design is appalling because it raises false hopes and adversely affects the control patients (because they may get angry, frustrated, disappointed, depressed, etc. about not receiving the extra services). I, too, am glad that Medicare is investigating better ways to deliver health care, but this study's design makes me angry.
My father does not know to which group he was assigned. But it's obvious that no nurse is talking to him about the plan for his care.
I don't see any way that this experiment could be done with informed consent and still be "blind."
I agree with the previous poster, the design of this study allows for a number of confounding factors to creep in and potentially skew results (the saddened, angry, etc. patient will do poorly relative to the patient that 'wins' and gets extra care/time/input from a nurse).
In response to Kling, the study could have been 'blinded' by:
#1. The IRB waiving the need for informed consent. If the care they are receiving is what they would have received while not in the study, why do they need to be consented? Or,
#2. Having a 'Nurse Coordinator' or someone acting the role, meet with the control patients, but do nothing to coordinate the care (i.e. - someone plays the nurse and sits with the patient and acts understanding, but provides no input to the real medical team that would alter the course of care. That way you eliminate the knowledge of treatment vs. control causing confounding bias, and you eliminate the variable of 'someone taking an interest in me and listening to what I have to say' as a placebo effect of the nurse manager.
While not perfect, it's an interesting study.
Caring and worrying for parents while they undergo treatment is not easy. I can appreciate what you are going through, as my mom underwent cancer treatment recently. Good Luck.