Parkinson's Disease Clinical Trial
Official title:
Nicotine Treatment of Impulsivity in Parkinson's Disease: A Pilot Study
The specific aims of this study are to examine whether treatment with transdermal nicotine improves computer-based laboratory and clinical measures of impulsive and compulsive behaviors in Parkinson's Disease subjects who have recently experienced an impulse control disorder.
In recent years, a group of behavior changes collectively called Impulse Control Disorders
(ICDs) have been identified in Parkinson's Disease (PD). ICDs have a broad range of possible
symptoms such as compulsive gambling, shopping, hypersexual behavior, overeating; spending
excessive amounts of time on hobbies, tasks, or other organized activities; walking or
driving without a goal or purpose; hoarding or overuse of PD medications. It is estimated
that as many as 30% of people with PD experience ICDs during the course of their condition.
ICDs are believed to occur due to effects of dopamine enhancing medications in areas of the
brain which regulate behavior (rather than their intended target areas that regulate
movement).
A reduction or discontinuation of PD medications can be helpful in reducing ICDs.
Unfortunately reduction in medication is often impractical or not possible because people
with PD rely on these medications to improve their movement symptoms. There are currently no
scientifically proven treatments for ICDs except for PD medication reductions.
Acetylcholine is a chemical in the brain which works to regulate the effects of dopamine. It
has been known for many years that nicotine imitates many of the actions of acetylcholine.
In preliminary studies, nicotine has been shown to reduce impulsive behavior in Attention
Deficit Hyperactivity Disorder. By administering nicotine across the skin using a patch, we
hope to better understand whether nicotine may act to improve impulse control disorders in
PD without needing to reduce or stop PD medications. Several studies have shown that
nicotine is tolerated well by people with PD, and does not appear to worsen motor/movement
symptoms. The amount of nicotine in each patch used in this study is the same as patches
that are used in people who are trying to quit smoking.
In this pilot within-subject crossover placebo-controlled study, subjects with a diagnosis
of Parkinson's Disease who have recently experiencing an impulse control disorder will be
enrolled. Subjects will randomized to one of two treatment groups. During the first portion
of the study, the first treatment group will receive transdermal nicotine (nicotine by skin
patch) and the second treatment group will receive an identical placebo patch which does not
contain any nicotine. Over the course of the study, each of the two groups will switch to
receive whichever treatment they were not initially receiving (for example-the first
treatment group will later receive the placebo patch and the second treatment group will
later receive the nicotine patch). Each treatment group will receive the nicotine patch or
placebo patch for an equal number of weeks, but at different times during the study.
Clinical and laboratory computer based measurements of impulsive and compulsive behaviors,
memory testing, sleep quality/ sleepiness, and Parkinson's disease symptoms will be assessed
at each visit.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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