Full Text View
Tabular View
No Study Results Posted
Related Studies
N-Acetyl Cysteine Plus Behavioral Therapy for Nicotine Dependent Pathological Gamblers
This study is currently recruiting participants.
Verified by Yale University, January 2010
First Received: August 25, 2009   Last Updated: January 29, 2010   History of Changes
Sponsor: Yale University
Collaborators: National Institute on Drug Abuse (NIDA)
University of Minnesota - Clinical and Translational Science Institute
Information provided by: Yale University
ClinicalTrials.gov Identifier: NCT00967005
  Purpose

The objective of this application is to examine whether, given its mechanism of action, the dietary supplement, N-acetyl cysteine (NAC) will reduce both tobacco use and pathological gamblers (PG) symptoms in nicotine dependent pathological gamblers.


Condition Intervention Phase
Gambling
Tobacco Use Disorder
Drug: N Acetyl Cysteine
Other: Sugar Pill
Phase II

Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Official Title: N-Acetyl Cysteine Plus Behavioral Therapy for Nicotine Dependent Pathological Gamblers

Resource links provided by NLM:


Further study details as provided by Yale University:

Primary Outcome Measures:
  • The primary outcome will be at least 4 weeks of continuous abstinence from tobacco at the end of the 12-week treatment period. This will be confirmed by cotinine <10 ng/ml and CO <8 ppm. [ Time Frame: 12 week ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Consistent with recent consensus on the assessment of PG severity, the main outcome measures will be money lost gambling per month. This will be assessed using the Gambling Timeline Followback (G-TLFB). [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 80
Study Start Date: September 2009
Estimated Study Completion Date: September 2011
Estimated Primary Completion Date: September 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
N Acetyl Cysteine: Experimental
The objective of this application is to examine whether, given its mechanism of action, the dietary supplement, N-acetyl cysteine (NAC) will reduce both tobacco use and PG symptoms in nicotine dependent pathological gamblers.
Drug: N Acetyl Cysteine
N-Acetyl Cysteine, 1200mg-3000mg each day for 24-weeks
Sugar Pill: Placebo Comparator Other: Sugar Pill
placebo control

Detailed Description:

Among US adults, 12.8% report nicotine dependence, and nicotine dependence is highly associated with a variety of DSM-IV Axis I and II disorders (Grant BF et al., 2004). Pathological gambling (PG), a serious public health problem with detrimental effects on individuals and families, and with an estimated yearly cost to society of 5 billion dollars due to lost jobs, debt, bankruptcy, and incarcerations, is associated with elevated proportions of nicotine dependence (41% - 55%), and tobacco smoking in clinical samples of pathological gamblers has been associated with increased gambling severity and more frequent psychiatric problems (Smart & Ferris, 1996; Crockfod & El-Guebaly, 1998; Shaffer et al., 1999; Petry & Oncken, 2002; Potenza et al., 2004; Grant et al., 2005; Falk et al., 2006; Fagan et al., 2007). In addition, research suggests that continued nicotine use is associated with greater rates of relapse among pathological gamblers who received behavioral therapy. Despite increased awareness of the relationship between nicotine dependence and PG, and the possible effects of nicotine dependence on gambling severity, no previous research has focused on how assessment and treatment of nicotine dependence may aid in the successful treatment of PG or smoking cessation. Preliminary research suggests that behavioral therapy using imaginal desensitization and motivational interviewing (IDMI) has shown promise in reducing the symptoms of PG (Grant et al., in press). Despite the efficacy of treatments for PG and nicotine dependence, relapse is common among individuals with nicotine dependence and PG. Preclinical studies have suggested that levels of glutamate within the nucleus accumbens mediate reward-seeking behavior and may underlie relapse seen in addictions. N-acetyl cysteine, a dietary supplement, amino acid and cysteine pro-drug, appears to modulate glutamate within the nucleus accumbens and has shown benefit in reducing the reward-seeking behavior in individuals with cocaine dependence and in pathological gamblers (Baker et al., 2003; LaRowe et al., 2006; Grant et al., 2006). If successful in treating nicotine dependent pathological gamblers, N-acetyl cysteine may serve as a viable, low-cost, and easily available treatment option for nicotine dependent pathological gamblers who receive behavioral therapy.

We therefore propose to examine how a dietary supplement, N-acetyl cysteine, used in combination with behavioral therapy, will affect both the urge to smoke and gamble in nicotine dependent pathological gamblers and smoking and gambling behaviors. We therefore propose a randomized placebo-controlled trial of N-acetyl cysteine or placebo with 80 nicotine dependent pathological gamblers who will all receive brief standardized smoking cessation treatment (Ask, Advise, and Refer model) for nicotine cessation and 6 sessions of IDMI for PG. We hypothesize that N-acetyl cysteine plus behavioral therapy will result in greater reduction in both nicotine dependence and PG symptoms during the acute treatment phase and will enhance greater long-term abstinence. Our research will contribute to an improved understanding of the treatment of nicotine-dependent pathological gamblers as well as a greater understanding of the treatment of co-occurring addictions. If our intervention is successful, it will have the potential to set a new standard of care for a range of psychiatric disorders that co-occur with nicotine dependence.

  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Male and female outpatients, age 18-75 years;
  2. Presence of current DSM-IV nicotine dependence and PG for at least 6 months duration;
  3. Stable psychotropic drug dose for a period of at least 3 months prior to study entry;
  4. Completion of complete blood count, urinalysis, liver function tests, thyroid function tests, and pregnancy test with no evidence of significant lab abnormalities;
  5. Signed informed consent

Exclusion Criteria:

  1. Subjects who are currently receiving individual or group therapy specifically for nicotine dependence or PG symptoms;
  2. Currently receiving pharmacotherapies for either nicotine dependence or pathological gambling;
  3. Subjects who have started attending Gamblers Anonymous within the 3 months prior to study initiation;
  4. Subjects who have an unstable and significant medical illness;
  5. Current clinically significant suicidality (score or 3 or 4 on item 3 of the Hamilton Depression Rating Scale) or any other disorder requiring immediate intervention;
  6. Lifetime history of bipolar disorder type I or II, dementia, or psychotic disorder;
  7. Current (past 12 months) DSM-IV substance abuse or dependence (except nicotine dependence);
  8. Borderline or antisocial personality disorder based on the SCID-II;
  9. Positive urine drug screen at screening;
  10. Asthma (given possible worsening of asthma due to NAC);
  11. Cognitive impairment that interferes with the capacity to understand and self-administer medication or provide written informed consent;
  12. Current pregnancy or lactation, or inadequate contraception in women of childbearing potential; and
  13. Previous treatment with NAC
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00967005

Contacts
Contact: Marc N Potenza, MD, PhD 203-974-7356 marc.potenza@yale.edu
Contact: Jon E Grant, MD, JD, MPH 612-273-9736 grant045@umn.edu

Locations
United States, Connecticut
Yale University School of Medicine Recruiting
New Haven, Connecticut, United States, 06519
Contact: Marc N Potenza, MD, PhD     203-974-7356     marc.potenza@yale.edu    
Contact: Scott A Bullock     203-974-7312     scott.bullock@yale.edu    
Principal Investigator: Marc N Potenza, MD, PhD            
United States, Minnesota
University of Minnesota School of Medicine Recruiting
Minneapolis, Minnesota, United States, 55454
Contact: Jon E Grant, MD, JD, MPH     612-273-9736     grant045@umn.edu    
Contact: Brian L Odlaug     612-627-4363     odla0019@umn.edu    
Principal Investigator: Jon E Grant, MD, JD, MPH            
Sub-Investigator: Brian L Odlaug            
Sponsors and Collaborators
Yale University
University of Minnesota - Clinical and Translational Science Institute
Investigators
Principal Investigator: Marc N Potenza, MD, PhD Yale University
Principal Investigator: Jon E Grant, MD, JD, MPH University of Minnesota - Clinical and Translational Science Institute
  More Information

No publications provided

Responsible Party: Yale University ( Marc N. Potenza, MD, PhD Associate Professor of Psychiatry and Child Study )
Study ID Numbers: 0908M70981, 1RC1DA028279-01
Study First Received: August 25, 2009
Last Updated: January 29, 2010
ClinicalTrials.gov Identifier: NCT00967005     History of Changes
Health Authority: United States: Food and Drug Administration

Keywords provided by Yale University:
N acetyl cysteine
Pathological gambling
Nicotine dependence

Additional relevant MeSH terms:
Acetylcysteine
N-monoacetylcystine
Respiratory System Agents
Anti-Infective Agents
Neurotransmitter Agents
Antioxidants
Cholinergic Agonists
Molecular Mechanisms of Pharmacological Action
Nicotinic Agonists
Physiological Effects of Drugs
Disorders of Environmental Origin
Cholinergic Agents
Nicotine
Mental Disorders
Therapeutic Uses
Free Radical Scavengers
Substance-Related Disorders
Ganglionic Stimulants
Antidotes
Tobacco Use Disorder
Antiviral Agents
Protective Agents
Pharmacologic Actions
Impulse Control Disorders
Gambling
Autonomic Agents
Expectorants
Peripheral Nervous System Agents

ClinicalTrials.gov processed this record on February 08, 2010