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. Author manuscript; available in PMC: 2020 Apr 1.
Published in final edited form as: Clin Trials. 2019 Apr;16(2):111–119. doi: 10.1177/1740774518816323

Table 2.

Sample sizes (N) for a secondary prevention trial enrolling persons with amyloidosis (state 2) with AD dementia (state 7) as the primary endpoint for three age distributions at enrollment. Follow-up durations are T=5 years and T=7 years. The intervention’s effects are θ24=0.50 and θ24 =0.67. P1 and P2 are the absolute risks of occurrence of the primary endpoint within T years. Power=0.90 and two sided significance level=.05.

θ24=0.50 θ24=0.67
T=5 years T=7 years T=5 years T=7years
AGE P1 P2 N P1 P2 N P1 P2 N P1 P2 N
Young 0.007 0.004 20727 0.018 0.010 8840 0.007 0.005 54951 0.018 0.013 23906
Uniform 0.014 0.008 10983 0.031 0.018 5633 0.014 0.010 29719 0.031 0.022 15635
Old 0.020 0.011 7898 0.042 0.024 4148 0.020 0.014 21424 0.042 0.031 11563

Age distributions are: young is w(a)=0.25 at ages a= 60, 65, 70 and 75; uniform is w(a)=0.167 at ages 60, 65, 70, 75, 80 and 85; old is w(a)=0.25 at ages 70, 75, 80 and 85. Incomplete follow-up is due only to death. N is the sample size from both groups combined (N/2 per group).