C.I.T.I. Training and IRB Certification
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C.I.T.I. Training and IRB Certification

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@HandsomeVariable

Questions and Answers

What does C.I.T.I. stand for?

  • Comprehensive Institutional Training Initiative
  • Central Institutional Training Initiative
  • Collaborative Institutional Training Initiative (correct)
  • Community Institutional Training Initiative
  • What is the role of the Institutional Review Board (IRB)?

    To approve research based on risk to the participants.

    Which of the following is NOT a condition for the IRB's involvement?

  • Uses research beyond observation
  • Performed research with animals
  • Receives federal funding
  • Participates in cooking competitions (correct)
  • Members of the IRB can have a vested interest in the research.

    <p>False</p> Signup and view all the answers

    What information should a researcher provide when proposing research to the IRB?

    <p>Participant centered information, including sample/population, contact method, research procedures, data usage, and possible risks.</p> Signup and view all the answers

    The risk/benefit ratio must always try to minimize the ______.

    <p>risk</p> Signup and view all the answers

    Which risk category involves no known risk to potential subjects?

    <p>Exempt research</p> Signup and view all the answers

    What constitutes expedited research?

    <p>Research involving minimal risk to human subjects, including physiological data collection.</p> Signup and view all the answers

    Full-review research has minimal risk to human subjects.

    <p>False</p> Signup and view all the answers

    Which item is NOT a criterion for the Centre's IRB eligibility quiz?

    <p>Use of devices in cooking</p> Signup and view all the answers

    Study Notes

    C.I.T.I. Training and Certification

    • Initiative developed by the University of Miami.
    • Offers online courses focused on research regulations and ethical standards.

    Institutional Review Board (IRB)

    • Approves research proposals based on participant risk assessment.
    • Mandatory for organizations receiving federal funding, conducting research on humans or animals, or utilizing research beyond mere observation.

    Member of the IRB

    • Composed of local professionals, including center professors, staff, and legal advisors.
    • Members must have no financial or professional stake in the research being reviewed to ensure impartiality.

    Proposing Research to the IRB

    • Must include participant-centered information such as:
      • Details on sample population.
      • Methods for contacting participants.
      • Outline of research procedures and questions.
      • Plan for data management.
      • Identification of potential risks to participants.

    Risk/Benefit Ratio

    • Focus on minimizing risk and maximizing benefits:
      • Risks can range from minimal discomfort to severe consequences (e.g., loss of sight).
      • Benefits could include small incentives (e.g., $5) or significant outcomes (e.g., successful phobia treatment).
    • Evaluation of risks and benefits varies based on time, cultural context, and situational factors.

    Risk Categories (Subjective)

    • Research classified into three categories:
      • Exempt research: minimal to no known risk.
      • Expedited research: involves minimal risk.
      • Full-review research: exceeds minimal risk.

    Exempt Research

    • Characterized by no known risks for participants.
    • May involve anonymous or publicly available data collection and naturalistic observation.
    • Requirement for PSY 205 course.

    Expedited Research

    • Involves minimal risk to participants, typically including:
      • Collection of physiological or biological data.
      • Use of photographs, videos, or audio recordings.
    • Commonly found in PSY 210 course.

    Full-Review Research

    • Involves research designs that pose greater than minimal risk to participants.

    Centre's IRB Eligibility Quiz

    • Criteria include:
      • No involvement with special populations, such as prisoners or children.
      • No use of deception in research design.
      • No risk of participant identification or stigmatization (e.g., disclosing GPA or body weight).
      • No potential for long-term adverse effects beyond normal stress levels.
      • Consideration of risks associated with physical interaction (e.g., using body sensors or equipment).

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    Description

    This quiz covers the essentials of C.I.T.I. training and the Institutional Review Board (IRB) processes. It includes information on the approval of research proposals, the roles of IRB members, and guidelines for proposing research. Test your knowledge on ethical standards and participant risk assessments in research.

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