Which of the Following Are the Three Principles Discussed in the Belmont Report?
The three core ethical principles of the Belmont Report are Respect for Persons, Beneficence, and Justice. Published in 1979, these principles guide the ethical conduct of research involving human subjects and map to informed consent, risk/benefit assessment, and fair subject selection.
The answer
The three ethical principles discussed in the Belmont Report are:
- Respect for Persons
- Beneficence
- Justice
Issued in 1979 by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, the Belmont Report established these three principles as the ethical foundation for all research involving human subjects in the United States. On the CITI exam, the correct choice is the option listing exactly Respect for Persons, Beneficence, and Justice—no more, no fewer.
What each principle means and how it is applied
The reason this trio matters is that each principle maps directly to a concrete research practice. This mapping is what most explainer pages leave out:
Respect for Persons → Informed consent. People must be treated as autonomous agents capable of making their own decisions, and those with diminished autonomy (children, prisoners, cognitively impaired individuals) are entitled to additional protection. In practice this principle produces the requirement for voluntary, informed consent.
Beneficence → Assessment of risks and benefits. Researchers must "do no harm" and maximize possible benefits while minimizing possible harms. In practice this principle drives the risk/benefit analysis that an IRB performs before approving a study.
Justice → Fair selection of subjects. The benefits and burdens of research must be distributed fairly, so that no group is unfairly targeted for risky research or unfairly denied access to benefits. In practice this principle governs equitable subject-selection criteria.
Why the other options are wrong
CITI questions surround the correct answer with plausible-sounding distractors. Watch for these:
"Autonomy, Beneficence, Non-maleficence, Justice" — This is the four-principle framework of biomedical ethics (Beauchamp and Childress), not the Belmont Report. The Belmont Report has three principles, and it uses "Respect for Persons," not "Autonomy," and folds non-maleficence into Beneficence.
"Respect for Persons, Beneficence, Integrity" — Integrity is not a Belmont principle; the third principle is Justice.
"Honesty, Objectivity, Confidentiality" — These are general research-conduct virtues, not the Belmont trio.
"Informed consent, Risk/benefit, Subject selection" — These are the applications of the principles, not the principles themselves. The question asks for the principles, so this is a classic trap.
The bigger picture
The Belmont Report was a direct response to research abuses—most notably the Tuskegee Syphilis Study—and it became the backbone of U.S. human-subjects regulations, including the Common Rule (45 CFR 46) that governs IRBs today. Remembering the report is easy if you pair each principle with its application: Respect for Persons → consent, Beneficence → risk/benefit, Justice → fair selection. That three-by-three anchor lets you both name the principles and explain how an IRB actually enforces them, which is exactly what the CITI exam expects.
| Respect for Persons | Treat individuals as autonomous; protect those with diminished autonomy | Informed consent |
| Beneficence | Maximize benefits and minimize harms ('do no harm') | Assessment of risks and benefits |
| Justice | Distribute research benefits and burdens fairly | Fair (equitable) selection of subjects |
Frequently asked
What are the three principles of the Belmont Report?
The three principles are Respect for Persons, Beneficence, and Justice. Respect for Persons requires informed consent, Beneficence requires weighing risks against benefits, and Justice requires the fair selection of research subjects and equitable distribution of benefits and burdens.
How is respect for persons applied in research?
Respect for Persons is applied through informed consent. Researchers must treat participants as autonomous decision-makers who voluntarily agree to participate, and must provide extra protections for people with diminished autonomy, such as children, prisoners, or cognitively impaired individuals.
What is the difference between beneficence and justice?
Beneficence concerns the balance of harms and benefits—maximizing benefits while minimizing risks to participants. Justice concerns fairness in who bears the burdens and who receives the benefits of research, ensuring no group is unfairly targeted or excluded.
What year was the Belmont Report published?
The Belmont Report was published in 1979 by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. It was written partly in response to abuses such as the Tuskegee Syphilis Study and shaped modern human-subjects protections.