SAS Exam A00-280 Topic 11 Question 58 Discussion

Actual exam question for SAS's A00-280 exam

Question #: 58
Topic #: 11

A Statistical Analysis Plan describes a clinical trial as "A 12 week, double-blind, placebo-controlled, randomized, multi-center study." Double-blind refers to which groups in this study?

Atreatment and control group

Binvestigator and subjects

Cstatistician and sponsor

Dsponsor and investigator

Show Suggested Answer

Suggested Answer: B

by Lajuana at May 20, 2024, 01:06 AM

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Oretha

6 months ago

B for sure. Anything else would just be a mess. Can you imagine the statistician being blinded? They'd be crunching numbers with their eyes closed!

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Ming

6 months ago

Hmm, let me think... I'll go with B. Double-blind just means the people administering and taking the treatment are both clueless. Keeps things nice and impartial.

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Whitney

6 months ago

C'mon, this is a classic double-blind study question. Of course it's B! The statistician and sponsor shouldn't be blinded, but the investigators and subjects need to be in the dark.

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Socorro

5 months ago

C) statistician and sponsor

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Buffy

5 months ago

B) investigator and subjects

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Mila

5 months ago

A) treatment and control group

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Edna

6 months ago

Definitely B. It's all about making sure there's no bias in the study. If the investigators and subjects don't know who's getting what, the results are much more reliable.

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Rosendo

5 months ago

B) investigator and subjects

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Alonzo

5 months ago

Definitely B. It's all about making sure there's no bias in the study. If the investigators and subjects don't know who's getting what, the results are much more reliable.

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Chuck

6 months ago

A) treatment and control group

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Sharika

6 months ago

The correct answer is B) investigator and subjects. In a double-blind study, neither the participants nor the researchers know who is receiving the treatment or the placebo.

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Paulina

5 months ago

B: Actually, it's B) investigator and subjects. In a double-blind study, neither the participants nor the researchers know who is receiving the treatment or the placebo.

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