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Impact of Smoking Cessation on Sleep - 5

Primary Purpose

Tobacco Use Cessation, Sleep Disorders

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Bupropion
Transdermal Nicotine Patch
Placebo Bupropion
Placebo transdermal nicotine patch
Sponsored by
National Institute on Drug Abuse (NIDA)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tobacco Use Cessation focused on measuring Nicotine dependence, Sleep disorders, smoking cessation, Relapse

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Meets DSM-IV criteria for nicotine dependence History of smoking at least 20 cigarettes each day for 2 years prior to enrollment Expired carbon monoxide level of at least 10 ppm Body mass index less than 30 kg/m2 Exclusion Criteria: Meets DSM-IV criteria for dependence on substances other than nicotine and caffeine Substance abuse within the year prior to enrollment History of DSM-IV diagnosis of schizophrenia, bipolar disorder, obsessive compulsive disorder, or chronic depression Current diagnosis of major depression History of neurological illness or trauma (e.g., stroke, seizure disorder, febrile seizures, electroconvulsive therapy) Family history of seizure disorder History of head injury with loss of consciousness for longer than 1 hour Currently diagnosed with a sleep disorder Currently diagnosed with anorexia or bulimia Severe or chronic cardiovascular, lung, kidney, or neurological disease Uncontrolled hypertension or diabetes Use of medications contraindicated with bupropion High frequency alcohol use or binge drinking in the month prior to enrollment Pregnant or breastfeeding

Sites / Locations

  • SRI International

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Placebo Comparator

Arm Label

A

B

C

D

Arm Description

Bupropion

Transdermal nicotine patch

Outcomes

Primary Outcome Measures

Pre- and post-cessation sleep measures by in-laboratory polysomnography

Secondary Outcome Measures

Smoking cessation status confirmed by carbon monoxide levels

Full Information

First Posted
August 18, 2005
Last Updated
January 11, 2017
Sponsor
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT00132821
Brief Title
Impact of Smoking Cessation on Sleep - 5
Official Title
Impact of Smoking Cessation on Sleep
Study Type
Interventional

2. Study Status

Record Verification Date
June 2009
Overall Recruitment Status
Completed
Study Start Date
August 2005 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Smoking is a major health problem with a direct link to elevated heart- and lung-related problems. Nicotine is highly addictive, which makes quitting difficult and relapse after quitting highly probable. Any type of sleep disturbance may make quitting even harder. The purpose of this study is to evaluate the effect of bupropion and nicotine replacement therapies (NRT) on sleep disturbances. In turn, this might show how such medications affect attempts at smoking cessation.
Detailed Description
The majority of attempts to quit smoking end in failure due to unpleasant withdrawal symptoms. One such symptom is sleep disturbances. Bupropion, effective in assisting with smoking cessation, commonly causes sleep disturbances as a medication side effect. In addition, a number of NRTs also cause sleep disturbances. This study will aim to characterize the effect of smoking cessation and smoking cessation treatments on sleep by measuring central and autonomic nervous system arousal. The study will also evaluate the impact of smoking cessation treatments on daytime sleepiness and mood as well as their effect on smoking relapse. Participants will be randomly assigned to one of four groups. Participants will receive either bupropion (150 mg for 3 days and 300 mg for 60 days) or placebo, starting one week prior to smoking quit day. They will then receive either active NRT (21 mg for 6 weeks, 14 mg for 1 week, and 7 mg for 1 week) or placebo, starting on quit day. Participants will be studied for up to 5 nights in a sleep lab. Sleep studies will include polysomnography measurements, including electrooculography of both eyes, activity of mentalis muscle and both anterior tibialis muscles, EEG, ECG, oxygen saturation, airflow, and respiratory efforts. Sleep studies will occur on the 2 nights prior to quit day, the quit night, and the 2 nights after quitting. Each sleep study will be followed by daytime measures. These will include a series of self-report instruments, sleepiness and performance measures, and physiological activity measures. Carbon monoxide levels will also be a daytime measurement and must fall below 10 ppm on the post quit days. All participants will receive bimonthly phone counseling for 12 months, starting on quit day. Participants will have follow-up evaluations at Months 3 and 12 in order to measure carbon monoxide levels and complete self-report instruments.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Use Cessation, Sleep Disorders
Keywords
Nicotine dependence, Sleep disorders, smoking cessation, Relapse

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
59 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Active Comparator
Arm Description
Bupropion
Arm Title
B
Arm Type
Active Comparator
Arm Description
Transdermal nicotine patch
Arm Title
C
Arm Type
Placebo Comparator
Arm Title
D
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Bupropion
Other Intervention Name(s)
Zyban
Intervention Description
Days 1-3, 150 mg Bupropion in am; days 4-63, 300 mg Bupropion (150 mg in am and 150 mg in pm)
Intervention Type
Drug
Intervention Name(s)
Transdermal Nicotine Patch
Intervention Description
21-mg nicotine patch applied in AM for 6 weeks, starting on the morning of quit day; 14-mg patch applied in AM for 2 weeks; 7-mg patch applied in AM for 1 week
Intervention Type
Drug
Intervention Name(s)
Placebo Bupropion
Intervention Description
Days 1-3, 150 mg placebo Bupropion in am; days 4-63, 300 mg placebo Bupropion (150 mg in am and 150 mg in pm)
Intervention Type
Drug
Intervention Name(s)
Placebo transdermal nicotine patch
Intervention Description
21-mg placebo nicotine patch applied in AM for 6 weeks, starting on the morning of quit day; 14-mg placebo patch applied in AM for 2 weeks; 7-mg placebo patch applied in AM for 1 week
Primary Outcome Measure Information:
Title
Pre- and post-cessation sleep measures by in-laboratory polysomnography
Time Frame
Up to 7 days post-cessation
Secondary Outcome Measure Information:
Title
Smoking cessation status confirmed by carbon monoxide levels
Time Frame
Up to 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Meets DSM-IV criteria for nicotine dependence History of smoking at least 20 cigarettes each day for 2 years prior to enrollment Expired carbon monoxide level of at least 10 ppm Body mass index less than 30 kg/m2 Exclusion Criteria: Meets DSM-IV criteria for dependence on substances other than nicotine and caffeine Substance abuse within the year prior to enrollment History of DSM-IV diagnosis of schizophrenia, bipolar disorder, obsessive compulsive disorder, or chronic depression Current diagnosis of major depression History of neurological illness or trauma (e.g., stroke, seizure disorder, febrile seizures, electroconvulsive therapy) Family history of seizure disorder History of head injury with loss of consciousness for longer than 1 hour Currently diagnosed with a sleep disorder Currently diagnosed with anorexia or bulimia Severe or chronic cardiovascular, lung, kidney, or neurological disease Uncontrolled hypertension or diabetes Use of medications contraindicated with bupropion High frequency alcohol use or binge drinking in the month prior to enrollment Pregnant or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gary Swan
Organizational Affiliation
SRI International
Official's Role
Principal Investigator
Facility Information:
Facility Name
SRI International
City
Menlo Park
State/Province
California
ZIP/Postal Code
94025
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
15801567
Citation
Colrain IM, Trinder J, Swan GE. The impact of smoking cessation on objective and subjective markers of sleep: review, synthesis, and recommendations. Nicotine Tob Res. 2004 Dec;6(6):913-25. doi: 10.1080/14622200412331324938.
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Impact of Smoking Cessation on Sleep - 5

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