TY - JOUR
T1 - The Apathy in Dementia Methylphenidate Trial 2 (ADMET 2)
T2 - Study protocol for a randomized controlled trial
AU - the ADMET 2 Research Group
AU - Scherer, Roberta W.
AU - Drye, Lea
AU - Mintzer, Jacobo
AU - Lanctôt, Krista
AU - Rosenberg, Paul
AU - Herrmann, Nathan
AU - Padala, Prasad
AU - Brawman-Mintzer, Olga
AU - Burke, William
AU - Craft, Suzanne
AU - Lerner, Alan J.
AU - Levey, Allan
AU - Porsteinsson, Anton
AU - van Dyck, Christopher H.
AU - Clark, David
AU - Battjes-Siler, Debra
AU - Smith, Stan
AU - O'Neil, Courtney
AU - Stocking, Nicole
AU - Perin, Jamie
AU - Shade, David
AU - Jones, Jennifer
AU - Holland, Stephanie
AU - Wentz, Alicia
AU - Chattopadhyay, Shumon
AU - Grove, Bethany
AU - Herrera, Stephanie
AU - Kaiser, Kristen
AU - Lears, Andie
AU - Broadnax, April
AU - Mohammed, Aisha
AU - Ryan, Laurie
AU - McKelvy, Alvin
AU - Rockwood, Kenneth
AU - Edland, Steve
AU - Turner, Raymond Scott
AU - Hodges, Debbie
AU - Jackson, Nicole
AU - Padala, Kalpana
AU - Batchuluun, Dawn
AU - Burke, Anna
AU - Grigaitis-Reyes, Michele
AU - DiLise-Russo, Marjoire
AU - Vadovicky, Shelia
AU - Favaro, Susan
AU - Hernandez, Mary Lou
AU - Autry, Lynn
AU - Hoffmann, Nicole
AU - Marano, Chris
AU - Burhanullah, Haroon
N1 - Publisher Copyright:
© 2018 The Author(s).
PY - 2018/1/18
Y1 - 2018/1/18
N2 - Background: Alzheimer's disease (AD) is characterized not only by cognitive and functional decline, but also often by the presence of neuropsychiatric symptoms. Apathy, which can be defined as a lack of motivation, is one of the most prevalent neuropsychiatric symptoms in AD and typically leads to a worse quality of life and greater burden for caregivers. Treatment options for apathy in AD are limited, but studies have examined the use of the amphetamine, methylphenidate. The Apathy in Dementia Methylphenidate Trial (ADMET) found that treatment of apathy in AD with methylphenidate was associated with significant improvement in apathy in two of three outcome measures, some evidence of improvement in global cognition, and minimal adverse events. However, the trial only enrolled 60 participants who were followed for only 6 weeks. A larger, longer-lasting trial is required to confirm these promising findings. Methods: The Apathy in Dementia Methylphenidate Trial 2 (ADMET 2) is a phase III, placebo-controlled, masked, 6-month, multi-center, randomized clinical trial targeted to enroll 200 participants with AD and apathy. Participants are randomly assigned 1:1 to 20 mg methylphenidate per day prepared as four over-encapsulated tablets or to matching placebo. The primary outcomes include (1) the mean difference in the Neuropsychiatric Inventory Apathy subscale scores measured as change from baseline to 6 months, and (2) the odds of having a given rating or better on the modified AD Cooperative Study Clinical Global Impression of Change ratings at month 6 compared with the baseline rating. Other outcomes include change in cognition, safety, and cost-effectiveness measured at monthly follow-up visits up to 6 months. Discussion: Given the prevalence of apathy in AD and its impact on both patients and caregivers, an intervention to alleviate apathy would be of great benefit to society. ADMET 2 follows on the promising results from the original ADMET to evaluate the efficacy of methylphenidate as a treatment for apathy in AD. With a larger sample size and longer follow up, ADMET 2 is poised to confirm or refute the original ADMET findings. Trial registration: ClinicalTrials.gov, NCT02346201. Registered on 26 January 2015.
AB - Background: Alzheimer's disease (AD) is characterized not only by cognitive and functional decline, but also often by the presence of neuropsychiatric symptoms. Apathy, which can be defined as a lack of motivation, is one of the most prevalent neuropsychiatric symptoms in AD and typically leads to a worse quality of life and greater burden for caregivers. Treatment options for apathy in AD are limited, but studies have examined the use of the amphetamine, methylphenidate. The Apathy in Dementia Methylphenidate Trial (ADMET) found that treatment of apathy in AD with methylphenidate was associated with significant improvement in apathy in two of three outcome measures, some evidence of improvement in global cognition, and minimal adverse events. However, the trial only enrolled 60 participants who were followed for only 6 weeks. A larger, longer-lasting trial is required to confirm these promising findings. Methods: The Apathy in Dementia Methylphenidate Trial 2 (ADMET 2) is a phase III, placebo-controlled, masked, 6-month, multi-center, randomized clinical trial targeted to enroll 200 participants with AD and apathy. Participants are randomly assigned 1:1 to 20 mg methylphenidate per day prepared as four over-encapsulated tablets or to matching placebo. The primary outcomes include (1) the mean difference in the Neuropsychiatric Inventory Apathy subscale scores measured as change from baseline to 6 months, and (2) the odds of having a given rating or better on the modified AD Cooperative Study Clinical Global Impression of Change ratings at month 6 compared with the baseline rating. Other outcomes include change in cognition, safety, and cost-effectiveness measured at monthly follow-up visits up to 6 months. Discussion: Given the prevalence of apathy in AD and its impact on both patients and caregivers, an intervention to alleviate apathy would be of great benefit to society. ADMET 2 follows on the promising results from the original ADMET to evaluate the efficacy of methylphenidate as a treatment for apathy in AD. With a larger sample size and longer follow up, ADMET 2 is poised to confirm or refute the original ADMET findings. Trial registration: ClinicalTrials.gov, NCT02346201. Registered on 26 January 2015.
UR - http://www.scopus.com/inward/record.url?scp=85040775562&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85040775562&partnerID=8YFLogxK
U2 - 10.1186/s13063-017-2406-5
DO - 10.1186/s13063-017-2406-5
M3 - Article
C2 - 29347996
AN - SCOPUS:85040775562
SN - 1745-6215
VL - 19
JO - Trials
JF - Trials
IS - 1
M1 - 46
ER -