In​ randomized, double-blind clinical trials of a new​ vaccine, infants were randomly divided into two groups. Subjects in group 1 received the new vaccine while subjects in group 2 received a control vaccine. After the second​ dose, 126 of 387 subjects in the experimental group​ (group 1) experienced drowsiness as a side effect. After the second​ dose, 158 of 574 of the subjects in the control group​ (group 2) experienced drowsiness

Holt Mcdougal Larson Pre-algebra: Student Edition 2012
1st Edition
ISBN:9780547587776
Author:HOLT MCDOUGAL
Publisher:HOLT MCDOUGAL
Chapter11: Data Analysis And Probability
Section: Chapter Questions
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In​ randomized, double-blind clinical trials of a new​ vaccine,
infants
were randomly divided into two groups. Subjects in group 1 received the new vaccine while subjects in group 2 received a control vaccine. After the second​ dose,
126
of
387
subjects in the experimental group​ (group 1) experienced
drowsiness
as a side effect. After the second​ dose,
158
of
574
of the subjects in the control group​ (group 2) experienced
drowsiness
as a side effect. Does the evidence suggest that a higher proportion of subjects in group 1 experienced
drowsiness
as a side effect than subjects in group 2 at the
α=0.01
level of​ significance?
Verify the model requirements. Select all that apply.
 
 
A.
The sample size is less than​ 5% of the population size for each sample.
 
B.
n1p11−p1≥10
and n2p21−p2≥10
 
C.
The samples are dependent.
 
D.
The sample size is more than​ 5% of the population size for each sample.
 
E.
The samples are independent.
 
F.
The data come from a population that is normally distributed.
 
Determine the null and alternative hypotheses.
 
H0​:
p1
 
less than<
equals=
greater than>
not equals≠
p2
H1​:
p1
 
less than<
equals=
not equals≠
greater than>
p2
 
Determine the​ P-value for this hypothesis test.
 
nothing
​(Round to three decimal places as​ needed.)
 
State the conclusion for this hypothesis test.
 
 
A.
Reject
H0.
There
is not
sufficient evidence to conclude that a higher proportion of subjects in group 1 experienced
drowsiness
as a side effect than subjects in group 2 at the
α=0.01
level of significance.
 
B.
Reject
H0.
There
is
sufficient evidence to conclude that a higher proportion of subjects in group 1 experienced
drowsiness
as a side effect than subjects in group 2 at the
α=0.01
level of significance.
 
C.
Do not reject
H0.
There
is
sufficient evidence to conclude that a higher proportion of subjects in group 1 experienced
drowsiness
as a side effect than subjects in group 2 at the
α=0.01
level of significance.
 
D.
Do not reject
H0.
There
is not
sufficient evidence to conclude that a higher proportion of subjects in group 1 experienced
drowsiness
as a side effect than subjects in group 2 at the
α=0.01
level of significance.
 
 
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