What role did the Tuskegee syphilis experiment play in the development of the Belmont Report?

Asked By: Kira Ordner | Last Updated: 18th January, 2020
Category: medical health infectious diseases
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The Tuskegee study and the Belmont report
The study was designed to demonstrate the need for establishing syphilis treatment programs by investigating the effects of untreated disease.

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Keeping this in view, what was the main ethical problem with the Tuskegee experiment?

The Tuskegee Study raised a host of ethical issues such as informed consent, racism, paternalism, unfair subject selection in research, maleficence, truth-telling and justice, among others.

Also Know, what was the purpose of the Tuskegee syphilis experiment? The purpose of the study was to determine whether penicillin could prevent, not just cure, syphilis infection. Some of those who became infected never received medical treatment.

Similarly, it is asked, how did the Tuskegee Study violate the principle of justice as outlined in the Belmont Report?

Obviously, researchers in the Tuskegee Syphilis Study violated all three of these principles, as participants were lied to about their condition, lied to about the treatment they were receiving, and selected based on race, gender, and economic class.

What laws were created because of the Tuskegee study?

After the Tuskegee Study, the government changed its research practices to prevent a repeat of the mistakes made in Tuskegee. In 1974, the National Research Act was signed into law, creating the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research .

38 Related Question Answers Found

Why was the Tuskegee syphilis experiment unethical?

Q. When did the U.S. Public Health Service Syphilis Study at Tuskegee become unethical? A. The study became unethical in the 1940s when penicillin became the recommended drug for treatment of syphilis and researchers did not offer it to the subjects.

Who benefited from the Tuskegee study?

It was called the “Tuskegee Study of Untreated Syphilis in the Negro Male.” The study initially involved 600 black men – 399 with syphilis, 201 who did not have the disease. The study was conducted without the benefit of patients' informed consent.

What were the effects of the publicity about the Tuskegee experiment?

Disclosure of the Tuskegee Study disrupted a slow convergence of black health outcomes with white health outcomes in the mid-20th century, accelerated an erosion of trust in doctors, and dampened health-seeking behavior and health-care utilization for black men.

How and when did information about the experiment come to the public's attention?

On July 25, 1972, the public learned that, over the course of the previous 40 years, a government medical experiment conducted in the Tuskegee, Ala., area had allowed hundreds of African-American men with syphilis to go untreated so that scientists could study the effects of the disease.

What was the outcome of the Tuskegee study?


The 40-year Tuskegee Study of Untreated Syphilis in the Negro Male study was a major violation of ethical standards. Researchers knowingly failed to treat patients appropriately after the 1940s validation of penicillin was found as an effective cure for the disease that they were studying.

Did the Tuskegee Airmen have syphilis?

Many Americans will associate Tuskegee with the famous black pilots of World War II. The now well-celebrated Tuskegee Airmen have received a number of honors after decades of neglect. The U.S. government injected the men with syphilis. They went untreated as human guinea pigs.

What is informed consent in research?

Informed Consent is a voluntary agreement to participate in research. It is not merely a form that is signed but is a process, in which the subject has an understanding of the research and its risks. Informed consent is essential before enrolling a participant and ongoing once enrolled.

Why was the Tuskegee study considered unethical quizlet?

7: Why was the Tuskegee Study considered unethical? A. Those conducting the study did not provide treatment for participants even after an effective treatment became available. Those conducting the study did not provide treatment for participants even after an effective treatment became available.

What are the 3 principles identified in the Belmont Report and what do they mean?

The Belmont Report summarizes ethical principles and guidelines for research involving human subjects. Three core principles are identified: respect for persons, beneficence, and justice. Three primary areas of application are also stated.

What is the Belmont report and why is it important?


The Belmont Report is one of the leading works concerning ethics and health care research. Its primary purpose is to protect subjects and participants in clinical trials or research studies. This report consists of 3 principles: beneficence, justice, and respect for persons.

Does virtue ethics support the Belmont Report?

The Belmont Report adheres to three basic principles: respect for persons, beneficence, and justice. Contemporary theories of Virtue Ethics do not support the Belmont Report. THE BELMONT REPORT 5 References Codes and Regulations.

Who created the Belmont Report?

The Belmont Report was written by the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research.

What was the Belmont report in response to?

The Belmont Report was written in response to the infamous Tuskegee Syphilis Study, in which African Americans with syphilis were lied to and denied treatment for more than 40 years. Many people died as a result, infected others with the disease, and passed congenital syphilis onto their children.

What is justice in the Belmont Report?

Justice, the third of these basic principles, is the main focus of this chapter. The Belmont Report states that "injustice arises from social, racial, sexual and cultural biases institutionalized in society." Women as a class were not the primary concern of the National Commission's work.

What are the two ethical convictions of Belmont Report?


The Belmont Report states that “respect for persons incorporates at least two ethical convictions: first, that individuals should be treated as autonomous agents, and second, that persons with diminished autonomy are entitled to protection.

Which basic principle from the Belmont report embodies the need for informed consent?

The Belmont principles include: (1) respect for persons, embodied in regulatory requirements for informed consent; (2) beneficence, embodied in regulations on the obligation to minimize risks and maximize research benefits; and (3) justice, reflecting in regulations requiring fair access of all populations to the

How do you ensure justice in research?

Ensuring justice in research begins with selecting subjects based on research needs rather than convenience. Inclusion and exclusion criteria should be explicit within the research protocol and followed to ensure equal opportunities to the participants (1, 4).