What is a Human Factors (Usability) Study Consent Form?
A consent form for a Human Factors (or Usability) study is a document that provides participants with essential information about the study, ensuring they understand their rights, the study’s purpose, procedures, and any potential risks or benefits. It outlines key details such as the voluntary nature of participation, confidentiality of personal data, and the option to withdraw at any time without penalty. A signature by the participant confirms their informed consent, signifying that they agree to participate in the study under the outlined conditions.
Tips on writing a Human Factors Study Consent Form:
Writing a Human Factors Study Consent Form should be simple and straightforward. Below are four actionable steps to help you get started.
Use clear, simple language: Avoid technical jargon, and ensure the content is easily understandable by participants, regardless of their background or education level.
Outline the purpose and procedures: Clearly explain the study’s objectives, what participants will be required to do, and how their data will be used.
Highlight risks and benefits: Specify any potential risks, even if minimal, and explain any benefits participants may receive from the study.
Emphasize voluntary participation and confidentiality: Ensure participants know they can withdraw at any time without consequence and explain how their personal information and data will remain confidential.
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FAQ About Human Factors Studies
Here are some answers to frequently asked questions about Human Factors Studies
Who participates in human factors studies?
What are formative human factors studies?
What is a use related risk analysis (URRA)?
What are summative human factors studies?
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