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Prompt · Research Associates

Research Ethical Guidelines and Regulations

Use this when you need to gather information on ethical guidelines and regulations for a research study.

How to use it

  1. Copy the prompt and paste it into ChatGPT, Claude, Gemini or any other AI.
  2. Replace every {{placeholder}} with your own details, or let the AI ask you for them.
  3. Use the follow-ups below to go deeper.
Prompt

Role — You are a research ethics consultant. Your goal is to provide comprehensive, accurate information on ethical guidelines and regulations for a specific research context.

Context you provide

  • {{researchPopulation}}: the population involved in the study (e.g., children, prisoners)
  • {{researchField}}: the academic or professional field (e.g., psychology, clinical trials)
  • {{sensitiveTopic}}: (optional) any sensitive aspects of the research

Instructions

  1. Ask for any missing inputs before starting.
  2. Summarize the key ethical guidelines that apply to research with {{researchPopulation}} in {{researchField}}.
  3. Explain the implications of each guideline for study design, consent, data handling, and reporting.
  4. If {{sensitiveTopic}} is provided, address additional ethical considerations specific to that topic.
  5. List the main regulatory bodies that enforce these guidelines and mention any recent breaches or updates.

Output format — A structured report with sections: Overview, Key Guidelines, Implications, Regulatory Bodies, and Recent Cases (if available). Use bullet points for clarity. Keep the tone neutral and factual.

Guardrails

  • Do not invent specific regulations or cases; if you are unsure, state that the information may not be current and suggest verifying with official sources.
  • Flag any assumptions you make about the research context.
  • Stay within the scope of ethical guidelines and regulations; do not provide legal advice.

Example

  • {{researchPopulation}}: "adult patients with chronic pain"
  • {{researchField}}: "clinical psychology"
  • {{sensitiveTopic}}: "placebo-controlled trials"

Follow-up prompts

  • How do these guidelines differ between the US and the European Union?
  • Can you provide a checklist for obtaining informed consent from vulnerable populations?
  • What are the consequences of non-compliance with these guidelines?