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When describing harms and benefits to potential trial participants, participant information leaflets are inadequate.

Laura CuddihyJeremy HowickEllen MurphyFrances Shiely
Published in: Trials (2024)
Significant variation exists in how potential trial benefits and harms are described to potential trial participants in PILs in our sample. Usage of the seven principles of good practice will promote consistency, ensure informed ethical decision-making and invoke trust and transparency. In the long term, a standardised PIL template is needed.
Keyphrases
  • phase iii
  • study protocol
  • decision making
  • clinical trial
  • phase ii
  • primary care
  • healthcare
  • human health
  • randomized controlled trial
  • open label
  • risk assessment
  • climate change
  • mass spectrometry
  • molecularly imprinted