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Psychological research involves studying human behaviour, which means researchers have a responsibility to protect the welfare and dignity of their participants. The British Psychological Society (BPS) publishes a Code of Ethics and Conduct that all psychologists in the UK must follow.
Participants must be given sufficient information about the study to make an informed decision about whether to take part. They must agree to participate voluntarily, without pressure or coercion.
Researchers should not mislead participants about the nature of the study. However, some studies require an element of deception to avoid demand characteristics.
Participants must be informed that they have the right to leave the study at any time, without giving a reason, and without any negative consequences.
Participants should not be exposed to any greater risk of physical or psychological harm than they would encounter in their everyday lives.
Participants' personal information and data must be kept confidential and not shared without their permission.
Researchers should respect participants' privacy. People should not be observed or studied in situations where they would not expect to be observed.
flowchart TD
A[BPS Code of Ethics] --> B[Informed consent]
A --> C[Deception]
A --> D[Right to withdraw]
A --> E[Protection from harm]
A --> F[Confidentiality]
A --> G[Privacy]
B --> B1[Voluntary agreement]
B --> B2[Parental consent if under 16]
C --> C1[Only if unavoidable]
C --> C2[Debrief afterwards]
D --> D1[Leave at any time]
D --> D2[Withdraw data later]
E --> E1[No greater risk than daily life]
F --> F1[Anonymous data storage]
G --> G1[Public vs private settings]
Before any research is conducted, the study must be approved by an ethics committee (also called an Institutional Review Board or IRB). The ethics committee:
| Study | Ethical Issue | How It Was Addressed (or Not) |
|---|---|---|
| Milgram (1963) | Deception, protection from harm (extreme distress) | Debriefed participants afterwards; but many experienced lasting distress |
| Asch (1951) | Deception (participants did not know the confederates were acting) | Debriefed after the study |
| Loftus and Palmer (1974) | Mild deception (different question wordings) | Low risk; debriefed |
| Piliavin et al. (1969) | No informed consent (participants were unsuspecting subway passengers) | Difficult to obtain consent in a field experiment |
Sometimes ethical principles conflict with each other or with the aims of the research:
Exam Tip: When evaluating a study ethically, identify the specific ethical principle involved (e.g. informed consent, protection from harm), explain how it was or was not followed, and discuss whether the potential harm was justified by the value of the findings.
Ethics in psychology is not just a checklist of rules to tick off. It is a way of thinking about the responsibility researchers have towards the people who take part in their studies. Every participant is a real person whose wellbeing, time and trust matter — and treating them well is both a moral obligation and a practical necessity. A study that damages participants loses public trust, discourages future participation and may prevent important research from being funded.
Modern ethical practice therefore goes beyond the written guidelines. It includes thinking carefully about the purpose of the research, the potential impact on participants' lives, and what the researcher would do if a participant became distressed or wished to withdraw. Experienced psychologists anticipate ethical issues in advance and build safeguards into the design, rather than reacting to problems as they arise.
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