A group in a clinical trial that receives a placebo or standard treatment for comparison.A control group is a baseline group in a clinical trial or experiment that does not receive the treatment being tested. Instead, it receives a placebo, a standard existing treatment, or no intervention at all. Its purpose is to provide a reference point so that any changes observed in the treatment group can be attributed to the treatment itself rather than to other factors like the natural course of a disease, the placebo effect, or random chance.
The concept of a control group became formalized in the early 20th century, notably with the 1948 British Medical Research Council trial of streptomycin for tuberculosis, which is widely considered the first properly randomized controlled trial.
Participants are randomly assigned to either the treatment group or the control group. The control group is treated identically to the treatment group in every way except for the intervention under study. By comparing outcomes between the two groups at the end of the trial, researchers can isolate the specific effect of the treatment. Blinding—where participants and sometimes researchers do not know who is in which group—further reduces bias.
Control groups are the gold standard in clinical trials for new drugs, vaccines, and medical procedures, and are also used in psychology, agriculture, and other experimental sciences.
The placebo effect is so powerful that even when people know they are taking a placebo, they can still experience real physiological improvements in some conditions.



