Nicotine Treatment of Impulsivity in Parkinson's Disease
Status: | Completed |
---|---|
Conditions: | Parkinsons Disease |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/2/2016 |
Start Date: | October 2010 |
End Date: | December 2013 |
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.
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.
(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.
Inclusion Criteria:
- A clinical diagnosis of idiopathic Parkinson's Disease based on movement disorders
specialist assessment using the National Institute of Neurological disorders and
Stroke (NINDS) criteria 17;
- demonstrated response to L-¬DOPA and/or dopamine agonists;
- Hoehn and Yahr19 stage 1 - 3 motor disability in the "on" medication state;
- stable PD and non-PD medications for at least 1 month prior to baseline;
- positive QUIP screening and confirmatory interview for current or prior ICD symptoms
36;
- Montreal Cognitive Assessment score > 24;
- impaired impulsive and/or compulsive responding compared to norms on Stop Signal Task
and/or Set-Shifting Task
- Global Deterioration Scale score24 of 1-2;
- Adequate visual and auditory acuity for neuropsychological testing;
- good general health with no additional diseases expected to interfere with the study;
- normal laboratory tests and ECG;
- female participants must be non-breastfeeding, post-menopausal or have been
surgically sterilized or have a negative urine pregnancy test at screening and
baseline visits with an acceptable form of contraception being used (see drug safety
section for details on acceptable contraception);
- Subjects will be taking no centrally active or anti or pro-cholinergic drugs;
- non¬smokers, defined as no cigarettes in the last 6 months
Exclusion Criteria:
- severe motor fluctuations;
- prior DBS surgery;
- Any significant systemic illness or unstable medical condition including serious
heart disease, severe asthma, severe or active ulcer disease, active thyroid disease,
pyloric stenosis epilepsy, or allergies to nicotine;
- clinically significant laboratory test abnormalities on the battery of screening
tests (hematology, chemistry, urinalysis, ECG);
- uncontrolled hypertension (systolic BP> 170 or diastolic BP> 100);
- Any current significant or unstable depression, anxiety, or psychosis
- history of obsessive-compulsive disorder
- use of any investigational drugs within 30 days or 5 half-¬lives, whichever is
longer, prior to screening
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