Trial of Nicotine Nasal Spray as an Aid for Smoking Cessation in Schizophrenia

This study has been completed.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
University of Medicine and Dentistry New Jersey
ClinicalTrials.gov Identifier:
NCT01010477
First received: November 6, 2009
Last updated: January 7, 2013
Last verified: January 2013

November 6, 2009
January 7, 2013
August 2009
July 2012   (final data collection date for primary outcome measure)
the quit rate of subjects who receive NNS and behavioral intervention will be significantly greater than the quit rate of the control group who will receive the placebo spray plus same behavioral intervention. [ Time Frame: 4 weeks ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01010477 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Trial of Nicotine Nasal Spray as an Aid for Smoking Cessation in Schizophrenia
Double-Blind, Placebo-Controlled Trial of Nicotine Nasal Spray as an Aid for Smoking Cessation in Schizophrenia

This R01 grant describes a randomized, double-blind, placebo-controlled trial of nicotine nasal spray (NNS) as an aid for smoking cessation in 60 individuals with schizophrenia. The objectives of this study are to determine the efficacy of NNS with behavioral intervention for smoking cessation in smokers with schizophrenia. It is hypothesized that the quit rate of subjects who receive NNS and behavioral intervention will be significantly greater than the quit rate of the control group who will receive the placebo spray plus same behavioral intervention. Quit rate is defined as the proportion of individuals who self report no tobacco use during weeks 5 through 8 confirmed by exhaled carbon monoxide (CO) less than 10 parts per million during these 4 weeks. The investigators will also assess abstinence rates at Study Weeks 12 and 20 on the NNS and at weeks 26 and 52 after the medication has been stopped. Since studies of this group suggest high relapse rates when treatments are discontinued (Evins et al., 2005; George et al., 2000; George et al., 2002a), the investigators will continue NNS treatment for a total of 20 weeks.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
  • Smoking Cessation
  • Schizophrenia
Drug: Nicotine Nasal Spray
minimum 8 doses of nasal spray per day; maximum of 5 doses per hour, no more than 40 doses per day
Other Name: Nicotrol
Experimental: Nicotine Nasal Spray
Intervention: Drug: Nicotine Nasal Spray
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
60
August 2012
July 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Subjects will be invited to participate in the study if they fulfill the following inclusion criteria:

    1. Meet DSM-IV diagnostic criteria for Schizophrenia
    2. Be 18 years of age or older
    3. Be daily smokers of 10 or more cigarettes per day (cpd)
    4. Have an expired CO level > 9 ppm
    5. Be motivated to quit smoking
    6. Be willing to adhere to the study protocol (e.g. provide samples, attend all visits)
    7. Be able to give informed consent
    8. Stable on their current atypical antipsychotic medication for at least one month.

Exclusion Criteria:

  • Subjects will be excluded based on any one of the following exclusion criteria:

    1. Current suicidal risk, including active suicidal ideation, recent suicidal behavior or suicide attempt in the past 30 days,
    2. Psychiatric hospitalization in the last 30 days
    3. Inability to read or understand the questionnaires in English
    4. Current pregnancy or lactation or plans to become pregnant in the next 12 months
    5. Regular use of non-cigarette forms of tobacco including cigars, pipes, smokeless tobacco
    6. Patients with significant cognitive impairment that may interfere with their study participation assessed as a Folstein Mini-Mental Status exam score of less than 22.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01010477
1R01DA024640-01A1, 1R01DA024640-01A1
Yes
University of Medicine and Dentistry New Jersey
University of Medicine and Dentistry New Jersey
National Institute on Drug Abuse (NIDA)
Principal Investigator: Jill M Williams, MD University of Medicine and Dentistry New Jersey
University of Medicine and Dentistry New Jersey
January 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP