What Is The Term For When Neither The Researcher Nor The Participants Know Who Is Receiving A Particular Treatment?

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A double-blind study is one in which neither the participants nor the experimenters know who is receiving a particular treatment. This procedure is utilized to prevent bias in research results.

Which of the following describes a study in which neither the participants nor the experimenters know which participants are in the control group?

Definition. The double-blind design describes an experimental procedure in which neither the participant nor the experimenter are aware of which group (i.e., experimental or control) each participant belongs to.

Which term describes a study where neither the researcher nor the participants know who is in the treatment group and who is not?

in a double-blind study , neither the participants nor the researchers working directly with those participants know who is getting the treatment and who is getting the placebo. This type of study is designed to reduce expectations and biases.

What is single blind and double-blind study?

A single-blind study masks the subjects from knowing which study treatment, if any, they are receiving. A double-blind study blinds both the subjects as well as the researchers to the treatment allocation .

What is a randomized double-blind study?

A double blind study is a randomized clinical trial in which: You as the patient don’t know if you’re receiving the experimental treatment, a standard treatment or a placebo, and.

What do you call a group of participants receiving a treatment?

Control groups in experiments

When researchers are interested in the impact of a new treatment, they randomly divide their study participants into at least two groups: The treatment group (also called the experimental group ) receives the treatment whose effect the researcher is interested in.

What is it called when a researcher is a participant?

Subject : subject or ‘human subject’ is a term describing the person who volunteers to be in a research experiment. Also called a research participant.

What is a control group in psychology?

The control group is composed of participants who do not receive the experimental treatment . ... They also closely resemble the participants who are in the experimental group or the individuals who receive the treatment. While they do not receive the treatment, they do play a vital role in the research process.

What is a scientific control group?

Control group, the standard to which comparisons are made in an experiment . ... A typical use of a control group is in an experiment in which the effect of a treatment is unknown and comparisons between the control group and the experimental group are used to measure the effect of the treatment.

What is an example of an experimental group?

An experimental group (sometimes called a treatment group) is a group that receives a treatment in an experiment. ... For example, a human experimental group could receive a new medication, a different form of counseling, or some vitamin supplements .

Which is better single blind or double-blind study?

In the case of investigating the effects of a drug that cures Alzheimer’s a double-blind study is beneficial compared to a single blind study. The participants are not aware if they received a placebo or a real drug, therefore their option on the treatment will less likely influence the outcome.

What is the purpose of single and double-blind studies?

In a single-blind study, patients do not know which study group they are in (for example whether they are taking the experimental drug or a placebo). In a double-blind study, neither the patients nor the researchers/doctors know which study group the patients are in.

Why use a triple blind study?

The purpose of triple-blinding procedures is to reduce assessment bias and to increase the accuracy and objectivity of clinical outcomes .

What is the meaning of double-blind study?

(DUH-bul-blind STUH-dee) A type of clinical trial in which neither the participants nor the researcher knows which treatment or intervention participants are receiving until the clinical trial is over . This makes results of the study less likely to be biased.

What are the disadvantages of a double-blind study?

  • It doesn’t reflect real-life circumstances. ...
  • Active placebos can interfere with the results. ...
  • It is not always possible to complete a double-blind study. ...
  • We do not fully understand the strength of the placebo effect. ...
  • Some people can have a negative response to a placebo.

Are double-blind studies ethical?

The point is that double-blinding is ethical only if it serves a scientific purpose . If its real purpose is to keep subjects in the trial when it is not in their best therapeutic interest to remain–a conflict of interest if ever there was one –then the blinds should be lifted.

James Park
Author
James Park
Dr. James Park is a medical doctor and health expert with a focus on disease prevention and wellness. He has written several publications on nutrition and fitness, and has been featured in various health magazines. Dr. Park's evidence-based approach to health will help you make informed decisions about your well-being.