Discussion of unethical experiments and their implications on ethics in research.
Importance of understanding these experiments in the context of current ethical standards.
Origin: Conducted by scientists at the University of Iowa in 1939.
Purpose: Aimed to investigate stuttering but involved gaslighting children into believing they had speech issues.
Total subjects: 22 orphan children.
Led by Professor Wendell Johnson.
Outcome: Survivors and families filed a lawsuit against the state of Iowa in 2007, receiving a total of $925,000 for psychological damage.
Ethical concerns: The American Speech-Language-Hearing Association prohibits experimentation on children with potential lasting harm.
Overview: Subjects administered what they believed were painful electric shocks to others when prompted by an authority figure in a lab coat.
Objective: Measured obedience to authority against personal morals.
Findings: 65% of subjects administered the maximum voltage despite signs of distress from the learner (actor).
Relation to historical events: Parallels drawn between Milgram's findings and the obedience shown in Nazi Germany.
Description: Experiment involving isolated baby monkeys to study the effects of maternal care on social development.
Experiment's design: Infants were given two surrogate mothers; one was comforting and the other provided nourishment but was frightening.
Research significance: Connections were made to reactive attachment disorder in humans, showing effects of maltreatment on psychological well-being.
Legislative impact: Resulted in greater scrutiny of animal research practices and more legislation for ethical treatment of animals.
Duration: 1932-1972, involving 399 men with untreated syphilis.
Misleading information: Participants were deceived about their health status (told they were receiving treatment for 'bad blood').
Ethical violations: No informed consent provided, and treatment was deliberately withheld despite the existence of a cure for syphilis.
Legal outcomes: Settlement in 1974 included $10,000,000 divided among affected group members.
Legal frameworks: Established post-experimentations, specifically the Nuremberg Code (1947) and the Declaration of Helsinki.
Key guidelines:
Voluntary consent from subjects.
Studies must yield fruitful results and ensure subject safety.
Need for ethical approval from Institutional Review Boards (IRBs).
Importance of informed consent and clear communication with subjects.
Risks associated with experiments must be minimized; protocols must be designed thoughtfully to avoid harm.
Need for checks and balances within research institutions (e.g., IRBs must ensure regulations are met).
Respect for persons: Ensuring autonomy and voluntary participation.
Beneficence: Maximizing benefits while minimizing risks.
Justice: Equitable selection of subjects and fairness in the distribution of research benefits.
Composition: At least one scientist, one non-scientist, and one non-affiliated member.
Function: Review research proposals for ethical standards, ensure participant protection, and monitor compliance throughout the research process.