HSCI 140 Final Essay

Submitted By Bianca-Auld
Words: 882
Pages: 4

HSCI 140

We talked about political influences in general, and especially when it comes to regulating more the Natural Products category. One one side we saw how the regulations of natural products was very poor, quasi inexistent in the US, more requirements in Canada, but the requirements for safety and efficacy in Canada were almost meaningless, and on the other side how the industry of Natural Products (small or big) was complaining about too many regulations, endangering their businesses, etc, and in one example threatening to sue Health Canada!
In the US, we can suspect that the lobby to keep things the way they are (minimal) is very strong. It is a huge business, and as we have seen, with very little benefit beyond the placebo effect and with many dangers, as we have seen.

“Equipoise and the ethics of clinical research”
“The ethics of clinical research requires equipoise‐‐a state of genuine uncertainty on the part of the clinical investigator regarding the comparative therapeutic merits of each arm in a trial. Should the investigator discover that one treatment is of superior therapeutic merit, he or she is ethically obliged to offer that treatment.”

Clinical equipoise, also known as the principle of equipoise, provides the ethical basis for medical research that involves assigning patients to different treatment arms of a clinical trial. The term was first used by Benjamin Freedman in 1987.[1]
An ethical dilemma arises in a clinical trial when the investigator(s) begin to believe that the treatment or intervention administered in one arm of the trial is significantly outperforming the other arms. A trial should begin with a null hypothesis, and there should exist no decisive evidence that the intervention or drug being tested will be superior to existing treatments or effective at all. As the trial progresses, the findings may provide sufficient evidence to convince the investigator of the intervention or drug’s efficacy. Once a certain threshold of evidence is passed, there is no longer genuine uncertainty about the most beneficial treatment, so there is an ethical imperative for the investigator to provide the superior intervention to all participants. Ethicists contest the location of this evidentiary threshold, with some suggesting that investigators should only continue the study until they are convinced that one of the treatments is better, and with others arguing that the study should continue until the evidence convinces the entire expert medical community.[citation needed]
In short, clinical equipoise means that there is genuine uncertainty in the expert medical community over whether a treatment will be beneficial. This applies also for off-label treatments performed before or during their required clinical trials.[citation needed]
The extent to which major research ethics policies endorse clinical equipoise varies. For instance, the Canadian Tri-Council Policy Statement endorses it; whereas, the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) does not. With regard to clinical equipoise in practice, there is evidence that industry-funded studies disproportionately favor the industry product, suggesting unfavorable conditions for clinical equipoise. In contrast, a series of studies of national cancer institute funded trials suggests an outcome pattern consistent with clinical equipoise.[2]

6 Things To Know About Massage Therapy for Health Purposes
The term “massage therapy” includes many techniques, and the type of massage given usually depends on your needs and physical condition. In general, massage therapists work