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Q: What type of experiment is it when only the subject does not know if they are receiving the real treatment or the placebo?
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What type of experiment is it when only the subject does not know it they are receiving the real treatment of the placebo?

If the experimenters know but the subject does not, it's called a "single blind" study. If the placebo is randomized and neither the subject nor the experimenters know which is the placebo, it's called a "double blind" study.


In an experiment a group that receives no treatment is called what?

A group that receives no treatment is called the control group. The control group is there to compare the results between a group that has been exposed to diffent conditions, and one that has not.


What is a placebo variable?

A placebo is a treatment, most commonly a medication of some kind, which is given to a subject with the pretense that it will treat a specific ailment when in fact the treatment will have no significant effect on the subject. The subject may report that the treatment has had a positive effect, when in fact the effect is entirely in the imagination of the subject. Therefore, a placebo variable is a factor that researchers in the medical field must consider when experimenting with new treatments, to decide whether the success of the treatment is due to the psychological or placebo effect of the treatment, or if the treatment itself is working.


A placebo is a medication that elicits a positive emotional response in an experimental subject?

Actually, a placebo is a substance or treatment with no therapeutic effect that is used as a control in medical research. It allows researchers to isolate the true effects of a treatment by comparing the results from the actual treatment group to those from the placebo group.


Single blind experiment?

In a double-blind experiment, neither the researchers or the human test subjects know if they are receiving the tested medication or just a placebo (a harmless substance). This eliminates any bias by either the subject (who may psychologically influence his condition) or the experimenter (who may otherwise see effects that are not due to the treatment). While there are logistical and ethical questions that make double-blind experiments difficult, the ultimate aim is to definitively establish whether a drug or treatment actually works.


What is double blind trial?

A double-blind study means that neither the test subject (human) or the researcher administering the study knows whether the test subject is receiving the experimental treatment or the control treatment. Often in human drug tests, the control treatment will be a placebo. This ensures that neither party can make any expectations as to whether they should or shouldn't be seeing results. This is important because sometimes researchers will botch their results to coincide with their hypothesis. This also ensures that both control and experimental groups experience the "placebo effect" more or less equally


What is double blind drug trial?

A double-blind study means that neither the test subject (human) or the researcher administering the study knows whether the test subject is receiving the experimental treatment or the control treatment. Often in human drug tests, the control treatment will be a placebo. This ensures that neither party can make any expectations as to whether they should or shouldn't be seeing results. This is important because sometimes researchers will botch their results to coincide with their hypothesis. This also ensures that both control and experimental groups experience the "placebo effect" more or less equally


What is a double blind drug?

A double-blind study means that neither the test subject (human) or the researcher administering the study knows whether the test subject is receiving the experimental treatment or the control treatment. Often in human drug tests, the control treatment will be a placebo. This ensures that neither party can make any expectations as to whether they should or shouldn't be seeing results. This is important because sometimes researchers will botch their results to coincide with their hypothesis. This also ensures that both control and experimental groups experience the "placebo effect" more or less equally


What is a double blind crossover study?

I want to know if a medication has the desired effect. I'm going to give half the subjects the 'live' med, and half will get a placebo. The subjects will not know which one they are getting. That's one level of "blind". Studies show that there is a measurable affect based on the fact that the person distributing the med's knows who is getting the med and who is getting the placebo. So I am going to package the med's and give them to the distributing nurse, and the nurse will not know who is getting the med and who is getting the placebo. That is "double blind" model.


What has the author Fabrizio Benedetti written?

Fabrizio Benedetti has written: 'Placebo effects' -- subject(s): Placebo (Medicine), Placebo Effect, Placebos, Suggestion, Therapeutic use, Treatment Outcome 'La tecnica del vertere negli epigrammi di Ausonio' -- subject(s): Ancient Rhetoric, History and criticism, Intellectual life, Latin Epigrams, Romans, Rome in literature, Sources


The group in an experiment that is not exposed to the tested variable is called the group?

An unexposed subject is the "control" for the experiment. The purpose is to establish an idea of what would normally occur outside the testing procedure. Similarly, in human tests, an inactive "placebo" is given to some subjects to verify that the changes occur independently of the psychosomatic (belief-driven) effects. In a "double blind' experiment, the person distributing the medication also does not know whether any particular individual is receiving the actual drug or a placebo. This is hidden in coded form until the results are recorded.


Does a patient have the right to know they are receiving a placebo?

If you are taking part in a medical or pharmaceutical test, no, you do not. You sign away those rights as a pre-requisite to becoming involved as a test subject. If this was NOT done in a test environment then the doctor would be committing malpractice.