Question

In: Statistics and Probability

A clinical trial is conducted to test a new medication designed to lower systolic blood pressure...

A clinical trial is conducted to test a new medication designed to lower systolic blood pressure (SBP). Participants are randomly assigned to receive the new medication or a placebo. The outcome is clinically significant SBP reduction after 30 days. The data are shown below. Compute the totals.

Significant Reduction in SBP

No Significant Reduction in SBP

Total

New Medication

44

76

Placebo

21

99

Total

  1. Compute the proportion of participants who experienced a significant reduction in SBP, given they received the new medication
    1. 0.3667
    2. 0.6769
    3. 0. 6333
    4. 0.175
    5. Some other answer (indicate):

  1. Compute the proportion of participants who experienced a significant reduction in SBP, given they received the placebo
    1. 0.825
    2. 0.3667
    3. 0.3231
    4. 0.175
    5. Some other answer (indicate):

  1. Generate a 90% confident interval for the true proportion of people experiencing a significant reduction in SBP given they received the new medication.
    1. (0.3635, 0.3699)
    2. (0.2943, 0.4391)
    3. (0.3155, 0.4179)
    4. (0.2684, 0.465)
    5. Some other answer (indicate):

Solutions

Expert Solution

Given,

Significant Reduction in SBP No Significant Reduction in SBP Total
New Medication 44 76 120
Placebo 21 99 120
Total 65 175 240

a. Compute the proportion of participants who experienced a significant reduction in SBP, given they received the new medication

Proportion of Participants who experienced significant reduction in SBP, given they received the new medication

= Number of Participants who received the new medication  and experienced significant reduction in SBP / Number of Participants who received the new medication

= 44/120 = 0.3667

Ans : a. 0.3667

b. Compute the proportion of participants who experienced a significant reduction in SBP, given they received the placebo

Proportion of Participants who experienced significant reduction in SBP, given they received the the placebo

= Number of Participants who received the the placebo  and experienced significant reduction in SBP / Number of Participants who received the the placebo

= 21/120 = 0.175

Ans : d. 0.175

c. Generate a 90% confident interval for the true proportion of people experiencing a significant reduction in SBP given they received the new medication

Confidence interval for true proportion :

n : sample size : Number of Participants who received the new medication = 120

Sample proportion of participants who experienced significant reduction in SBP, given they received the new medication

= Number of Participants who received the new medication  and experienced significant reduction in SBP / Number of Participants who received the new medication

= 44/120 = 0.3667

Confidence Level 90%
(= 100-90/100=10/100 ) = 0.1 0.1
/2 (=0.1/2=0.05) 0.05
1.6449

90% confident interval for the true proportion of people experiencing a significant reduction in SBP given they received the new medication

90% confident interval for the true proportion of people experiencing a significant reduction in SBP given they received the new medication = (0.2943, 0.4391)

Ans : b. (0.2943, 0.4391)


Related Solutions

A clinical trial is planned to compare an experimental medication designed to lower blood pressure to...
A clinical trial is planned to compare an experimental medication designed to lower blood pressure to a placebo. Before starting the trial, a pilot study is conducted involving 7 participants. The objective of the study is to assess how systolic blood pressure changes over time untreated. Systolic blood pressures are measured at baseline and again 4 weeks later. Is there a statistically significant difference in blood pressures over time? Run the test at a 5% level of significance. Baseline           120     ...
A clinical trial is planned to compare an experimental medication designed to lower blood pressure to...
A clinical trial is planned to compare an experimental medication designed to lower blood pressure to a placebo. Patients are enrolled and randomized to either the experimental medication or the placebo. The data shown below are data collected at the end of the study after 6 weeks on the assigned treatment. Experimental (n=100) Placebo (n=100) Mean (SD) Systolic Blood Pressure 120.2 (15.4) 131.4 (18.9) % Hypertensive 14% 22% % With Side Effects 6% 8% Is there a significant difference in...
A clinical trial is planned to compare an experimental medication designed to lower blood pressure to...
A clinical trial is planned to compare an experimental medication designed to lower blood pressure to a placebo. Before starting the trial, a pilot study is conducted involving eight participants. The objective of the study is to assess how systolic blood pressure changes over time untreated. Systolic blood pressures are measured at baseline and again 4 weeks later Is there a statistically significant difference in blood pressures over time? Run the test at a 5% level of significance. Give each...
A medical researcher wants to begin a clinical trial that involves systolic blood pressure (SBP) and...
A medical researcher wants to begin a clinical trial that involves systolic blood pressure (SBP) and cadmium (Cd) levels. However, before starting the study, the researcher wants to confirm that higher SPB is associated with lower Cd levels. Below are the SBP and Cd measurements for a sample a participants. What can the researcher conclude with an α of 0.10? SBP Cd 169 183 115 113 182 126 179 127 148 160 140 55.5 55.7 55.8 55.9 55.5 55.7 55.6...
A medical researcher wants to begin a clinical trial that involves systolic blood pressure (SBP) and...
A medical researcher wants to begin a clinical trial that involves systolic blood pressure (SBP) and cadmium (Cd) levels. However, before starting the study, the researcher needs to know if there is a relationship between SBP and Cd. Below are the SBP and Cd measurements for a sample a participants. What can the researcher conclude with α = 0.05? SBP Cd 169 161 115 113 182 126 179 127 148 160 140 55.9 55.7 55.7 55.5 55.9 55.8 55.8 55.5...
The drugs Telmisartan and Ramipril are designed to reduce high blood pressure. In a clinical trial...
The drugs Telmisartan and Ramipril are designed to reduce high blood pressure. In a clinical trial to compare the effectiveness of these drugs in preventing heart attacks, patients were divided into three groups. One group took a telmisartan tablet daily, another group a rampipril tablet daily, and the third group too both. Fatal Heart Attack Nonfatal Heart Attack No Heart Attack Telmisartan only 598 431 7513 Rampipril only 603 400 7573 Both drugs 1821 1255 7458 a) Describe the observational...
A clinical trial was conducted to test whether medication A could effectively be used to reduce...
A clinical trial was conducted to test whether medication A could effectively be used to reduce the risk of a special disease among people with high risk. The results at the end of the study are listed on the table below with disease without disease total medication A 99 3377 3476 placebo 174 3098 3272 Keep 4 decimal points for your calculations in Q1 - 4, 6 - 8. 1. P(disease| medication A) = Blank 1. Fill in the blank,...
21.HE.B: Captopril is a drug designed to lower systolic blood pressure. When subjects were treated with...
21.HE.B: Captopril is a drug designed to lower systolic blood pressure. When subjects were treated with this drug, their systolic blood pressure readings (in mm Hg) were measured before and after the drug was taken. The results are in the accompanying table on the next page. (a)      Go through “The Drill” for paired t-tests (Use a 0.05 α-level and the corresponding confidence interval.)           The Drill: Assumptions and Conditions Paired Data Condition The data must be paired. Only use pairing...
In a clinical trial to study if an experimental drug can lower diastolic blood pressure, 780...
In a clinical trial to study if an experimental drug can lower diastolic blood pressure, 780 participants suffering from high blood pressure were randomly assigned to one of three groups. Over a one-month period, the first group received a low dosage of the experimental drug, the second group received a high dosage of the drug, and the third group received a placebo. Neither the patients nor those analyzing the results knew what type of treatment each patient received. The diastolic...
A clinical trial is run to look at the efficacy of a new blood pressure drug....
A clinical trial is run to look at the efficacy of a new blood pressure drug. Patients with a diagnosis of hypertension (high blood pressure) are recruited to participate in the trial and randomized to receive either the new drug or placebo. Participants take the assigned drug for 12 weeks and their blood pressure status is recorded. At the end of the trial, participants are classified as still having hypertension or not. The data are shown here: Group Number with...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT