The responsiveness of outcome measures used in antidementia drug trials has
had little formal analysis, but it can be crucial to the interpretation of
a medication's effectiveness. The authors report the responsiveness of out
come measures from the Canadian trial of linopirdine, a novel phenylinodoli
none, estimated using an effect size statistic. The effect sizes ranged fro
m 0.10-0.26, with the cognitive and functional measures yielding estimates
greater than 0.20, a level held to be clinically detectable. All of the sta
ndard measures used in this trial, save one, performed better than the glob
al clinical measure. The global clinical measure used in this study may hav
e been too insensitive to detect minimal clinical change.