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Health Psychology

Ethics of using human participants to study drugs

  • 3 things to know
  • Papers 2 and 3

Overview

Recall questions on informed consent, the right to withdraw, protection from physical and psychological harm, confidentiality, deception and debriefing, ethics committees, safeguards for dependent participants, cost-benefit analysis, and placebo and double-blind designs.

What you need to know

Answer each one before you reveal it.

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Study

Give an example of an additional safeguard that might be used when researching drug effects with vulnerable participants.

Key term

What does full disclosure of study purpose mean in the context of informed consent for drug studies?

Key term

Why must researchers explain potential risks and side effects to participants before a drug study begins?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    Why is informed consent an important ethical consideration in human drug studies?

    Model answer

    Participants must be fully informed about the nature of the study and any potential risks before agreeing to take part

  2. 2

    What does the right to withdraw mean in the context of human drug research?

    Model answer

    Participants must be free to leave the study at any time without penalty or pressure to continue

  3. 3

    Why is protection from harm an ethical consideration in human drug studies?

    Model answer

    Researchers must ensure participants are not exposed to physical or psychological harm from the drugs or procedures used in the study

  4. 4

    Why is confidentiality particularly important as an ethical consideration in human drug research?

    Model answer

    Because participants may disclose illegal behaviours, their data must be kept confidential to protect them from legal or social consequences

  5. 5

    What does full disclosure of study purpose mean in the context of informed consent for drug studies?

    Model answer

    Participants must be fully informed about the nature and aims of the research before agreeing to take part.

  6. 6

    Why must researchers explain potential risks and side effects to participants before a drug study begins?

    Model answer

    So participants can make an informed decision about whether to take part, understanding what physical or psychological effects they might experience.

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