The purpose of this study is to examine the influence of the instruction on the use of Aricept with educational brochure on the 48-week medication persistence and to assess the reasons for discontinuation.
To examine the influence of the instruction on the use of Aricept with educational brochure comparing to the ordinary instruction on the 48-week medication persistence and to assess the reasons for discontinuation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
125
Instruction with educational brochure
Instruction as per usual practice
Shonan Fujisawa Tokushukai Hospital
Fujisawa, Kanagawa, Japan
Number of Participants With Medication Continuation
Number of Participants who Continue the Medication for 48 weeks
Time frame: 48 weeks
Reasons for Discontinuation
Reasons for discontinuation of the Medication
Time frame: 48 weeks
Number of Participants With Medication Discontinuation Due to Change to Alicept or Generics
Number of Participants who descontinue the Clinical Trial Medication due to Change to Alicept (not for clinical trial) or Generics
Time frame: 48 weeks
Adverse Events
Adverse Events for each arm
Time frame: Week 2, 12, 24, 48
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