
A control is an experimental condition that provides a baseline for comparison. It does not receive the experimental treatment, or it receives an established standard, placebo or alternative condition.
For example, imagine that researchers want to test whether a new fertilizer increases plant growth. One group of plants receives the fertilizer, while the control group does not. If both groups otherwise receive the same water, light and soil, differences in growth may be associated with the fertilizer.
The control does not prove causation by itself. Researchers must also use appropriate sampling, measurement and analysis methods.
These terms are related but should not be used interchangeably.
A control is the baseline condition or reference used for comparison.
A control group is a collection of participants, samples or test units assigned to the baseline condition.
In a clinical trial, the control group might receive a placebo, an existing treatment or no treatment. The experimental group receives the intervention being studied.
The NCBI Bookshelf describes a control group as the comparison group that helps investigators determine whether an observed effect results from the experimental intervention or from other factors.
A controlled variable is a factor researchers try to keep consistent across all experimental conditions.
In the fertilizer example:
An experiment may have controlled variables even when it does not have a separate control group.
Most experiments involve independent, dependent and controlled variables.
The independent variable is the factor the researcher deliberately changes.
Examples include:
A clear experiment typically changes one primary independent variable at a time.
The dependent variable is the outcome researchers measure.
Examples include:
The dependent variable may change in response to the independent variable.
Controlled variables are factors kept as consistent as possible.
Examples include:
Controlled variables reduce the likelihood that another factor explains the observed result.
A confounding variable is an outside factor associated with both the independent variable and the outcome. It can create a misleading relationship if it is not addressed.
Researchers may use randomization, matching, statistical adjustment or design restrictions to reduce confounding.
Different experiments require different control conditions.
A negative control is expected not to produce the effect being tested.
For example, plants receiving no fertilizer can serve as a negative control when testing a growth treatment. If the negative control unexpectedly changes, the researcher may need to investigate contamination or procedural problems.
A positive control uses a condition already known to produce an effect.
For example, researchers testing a new disinfectant might compare it with an established disinfectant. If the positive control fails, there may be a problem with the procedure or measurement.
A placebo resembles the experimental treatment but lacks its active component. Placebos can help researchers distinguish treatment effects from participants’ expectations.
Placebo controls are associated with human research and require appropriate ethical oversight.
An active control receives an established treatment. Researchers can compare a new intervention with the current standard rather than with no treatment.
A no-treatment group does not receive the experimental intervention. Researchers continue to observe and measure this group during the study.
A historical control uses data collected from a previous study or outside population.
External controls may be useful when a concurrent control is impractical or unethical. However, differences in participants, time periods and measurement methods can make the comparison less reliable.
The experimental group receives the independent variable or intervention being tested. The control group receives the baseline condition.
For a valid comparison, researchers try to make the groups similar except for the intervention.
In randomized research, participants are assigned to groups by chance. Randomization can reduce selection bias and help distribute known and unknown characteristics across groups. It does not guarantee that the groups will be identical, particularly in small samples.
Controls help researchers:
Without a meaningful comparison, researchers may observe a change but be unable to determine why it occurred.
Use the following steps to design an appropriate control.
Write a specific question describing what you want to test.
For example:
Does adding 10 grams of fertilizer per week increase the average height of tomato plants over six weeks?
This question identifies the intervention, measurement and time period.
A hypothesis predicts the relationship between the independent and dependent variables.
For example:
Tomato plants receiving 10 grams of fertilizer per week will grow taller than plants receiving no fertilizer.
A good hypothesis can be evaluated using observable data.
Determine the factor you intend to change. In the example, the independent variable is fertilizer treatment.
If you test several fertilizer amounts, each dosage becomes a level of the independent variable.
Choose an outcome that can be measured consistently. Plant height may be measured in centimeters at the same time each week.
Avoid vague outcomes such as “plants look healthier” unless you define a reliable rating method.
List other factors that could influence the outcome.
For the plant experiment, keep the following consistent:
Perfect control is rarely possible, but careful procedures can reduce unnecessary variation.
Choose the most appropriate baseline. In this example, the control plants receive no fertilizer while all other procedures remain the same.
In another experiment, the correct control might be an existing product, placebo or standard process.
Assign participants, samples or objects to the experimental and control conditions. Random assignment is useful when practical and ethical.
Document the method so another researcher can understand how the groups were created.
Follow the same procedure for every group except for the planned difference in the independent variable.
Use consistent:
Compare the dependent-variable measurements for the experimental and control conditions.
Analysis may involve:
The appropriate method depends on the research question and data.
Determine whether the results support the hypothesis. Consider alternative explanations, measurement limitations and sample size.
A difference between groups may reflect the intervention, chance, bias or an uncontrolled factor. The conclusion should reflect the strength of the evidence.
A researcher wants to determine whether a new fertilizer improves plant growth.
The experimental design includes:
If the treated plants grow more, the fertilizer may have contributed to the difference. Repeated trials can help determine whether the result is consistent.
A company wants to test whether a redesigned landing page increases registrations.
The original page serves as the control, while the redesigned page is the experimental condition.
The company randomly sends visitors to one version and compares registration rates. Factors such as traffic source, device and campaign timing should be monitored because they may affect the result.
This type of experiment is commonly called an A/B test.
A manufacturer wants to determine whether a new production process improves product durability.
Products made with the existing process form the control group. Products made with the new process form the experimental group.
Both groups should use comparable materials and undergo the same durability test. This helps isolate the effect of the production process.
A control group is the baseline comparison. Controlled variables are the conditions kept consistent across groups.
If researchers change several variables at once, they may not know which one caused the result.
Major differences between the experimental and control groups can introduce bias.
Using different equipment, instructions or timing can create artificial differences.
The control should answer the research question. A no-treatment group may not be appropriate when the objective is to compare a new process with the existing standard.
Some experiments cannot ethically withhold an established treatment or expose participants to unnecessary risk. Human and animal research may require formal review and informed consent.
Professionals who may design or interpret controlled experiments include:
The exact standards vary by industry and the level of risk involved.

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No. Some experiments compare different levels of an independent variable without a separate untreated group. However, experiments generally need controlled variables and a meaningful basis for comparison.
A control is a baseline condition used for comparison. A constant, or controlled variable, is a factor kept consistent throughout the experiment.
Yes. An active control group may receive an established treatment, while the experimental group receives the new treatment being evaluated.
Random assignment can reduce selection bias and make experimental and control groups more comparable at the beginning of a study. It strengthens the ability to associate differences with the tested intervention.