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Study Design & Methodology Flashcards

7 cards from real CPI practice questions. Tap to flip, then mark Knew It or Still Learning โ€” missed cards come back until you master them.

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  1. Which of the following is an example of an adaptive trial design?

    Answer: Pre-specified sample size reestimation at interim

    Adaptive designs allow pre-specified modifications (such as sample size reestimation) based on interim data while maintaining trial integrity.

  2. In a crossover trial, the 'washout period' serves to:

    Answer: Eliminate carryover effects from prior treatment

    The washout period allows prior treatment effects to dissipate before participants receive the next treatment, preventing carryover bias.

  3. A researcher compares outcomes between patients who chose drug A versus drug B without randomization. The main methodological threat is:

    Answer: Confounding by indication

    Confounding by indication occurs when the reason for choosing a treatment (indication) is also related to the outcome, distorting effect estimates.

  4. The CONSORT statement was developed primarily to improve reporting of:

    Answer: Randomized controlled trials

    CONSORT (Consolidated Standards of Reporting Trials) provides a checklist and flow diagram to improve transparency in RCT reporting.

  5. Which bias can occur when study participants who drop out differ systematically from those who complete the study?

    Answer: Attrition bias

    Attrition bias (loss-to-follow-up bias) occurs when dropouts differ from completers in ways that affect the outcome, distorting results.

  6. A Phase I clinical trial primarily aims to:

    Answer: Determine maximum tolerated dose and safety profile

    Phase I trials focus on safety, pharmacokinetics, and determining the maximum tolerated dose, typically in a small number of participants.

  7. Which of the following best describes a 'pragmatic' clinical trial?

    Answer: Real-world conditions testing whether a treatment works in practice

    Pragmatic trials test interventions under real-world clinical conditions with broad eligibility to assess effectiveness in routine practice.