Alzheimer's Disease Clinical Trial
Official title:
Apathy in Dementia Methylphenidate Trial (ADMET)
The Apathy in Dementia Methylphenidate Trial (ADMET) is a masked, placebo-controlled trial that will examine the efficacy and safety of methylphenidate for the treatment of clinically significant apathy in patients with Alzheimer's dementia.
The Apathy in Dementia Methylphenidate Trial (ADMET), funded by the National Institute of
Aging, is a Phase II, placebo-controlled, masked, 3-center randomized clinical trial. ADMET
will enroll 60 patients with Alzheimer's disease (AD) and significant apathy from outpatient,
nursing home, and assisted living facilities along with their primary caregiver. Eligible and
willing patients will be randomly assigned to methylphenidate (20 mg per day) or placebo. At
baseline and each in-person follow-up visit, all caregivers and patients will be provided
with a standardized psychosocial intervention consisting of a counseling session, provision
of educational materials, and 24-hour availability for crises. Efficacy and safety outcomes
will be measured at baseline and at in-person follow-up visits at 2, 4, and 6 weeks following
randomization. Telephone contact will take place at 1, 3, and 5 weeks after randomization.
ADMET has 80% power to detect a difference of at least 3.3 in change in the Apathy Evaluation
Scale scores between the two treatment groups. It also has 80% power to detect an absolute
difference of 35% or more in the change in the proportion of study participants improving on
te Clinical Global Impression of Change, given that 20% to 305 of participants in the placebo
group show improvement.
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