Examining the Effectiveness of the Nicotine Patch in Male and Female Smokers - 2
Status: | Completed |
---|---|
Conditions: | Smoking Cessation, Tobacco Consumers |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - 50 |
Updated: | 1/13/2017 |
Start Date: | May 2004 |
End Date: | June 2007 |
Effects of Transdermal Nicotine on Tobacco Withdrawal and the Effects of Smoking in Men and Women
Treatment studies have demonstrated that current smoking cessation techniques are less
effective for women. The purpose of this study is to determine the role that gender plays on
the effectiveness of nicotine replacement therapy. This may lead to improved cessation
interventions for all smokers, particularly women.
effective for women. The purpose of this study is to determine the role that gender plays on
the effectiveness of nicotine replacement therapy. This may lead to improved cessation
interventions for all smokers, particularly women.
Currently, about 70 percent of smokers who try to quit by using smoking cessation treatments
are unsuccessful. Treatment studies have demonstrated that current smoking cessation
techniques are less effective for women. There is no clear explanation for this difference,
but it may involve a differential response to nicotine replacement treatments (NRTs) and/or
smoking-related stimuli. For women, NRT may be less effective at suppressing withdrawal or
blunting the effects of smoking during a quit attempt. Women may also be more sensitive to
smoking-related stimuli, such as the taste, sight, and smell of smoke. Tailoring treatment
to the separate needs of subgroups, such as men and women, may produce better outcomes. The
purpose of this study is to assess the influence of gender on the effectiveness of
transdermal nicotine treatment in a group of male and female smokers.
Participants in this double-blind, dose-comparison study will complete separate sessions in
a random order.
Each session will last approximately 6.5 hours and will correspond to a specific transdermal
patch dose (0, 7, 14, or 21 mg). Objectively verified cigarette abstinence will be required
before each session. Sessions will occur at least 48 hours apart to avoid carryover.
Cognitive, behavioral, subjective, and physiological measures will occur during study
visits. Specifically, the NRT dose response to tobacco suppression and cigarette blunting
effects will be compared in women and men.
are unsuccessful. Treatment studies have demonstrated that current smoking cessation
techniques are less effective for women. There is no clear explanation for this difference,
but it may involve a differential response to nicotine replacement treatments (NRTs) and/or
smoking-related stimuli. For women, NRT may be less effective at suppressing withdrawal or
blunting the effects of smoking during a quit attempt. Women may also be more sensitive to
smoking-related stimuli, such as the taste, sight, and smell of smoke. Tailoring treatment
to the separate needs of subgroups, such as men and women, may produce better outcomes. The
purpose of this study is to assess the influence of gender on the effectiveness of
transdermal nicotine treatment in a group of male and female smokers.
Participants in this double-blind, dose-comparison study will complete separate sessions in
a random order.
Each session will last approximately 6.5 hours and will correspond to a specific transdermal
patch dose (0, 7, 14, or 21 mg). Objectively verified cigarette abstinence will be required
before each session. Sessions will occur at least 48 hours apart to avoid carryover.
Cognitive, behavioral, subjective, and physiological measures will occur during study
visits. Specifically, the NRT dose response to tobacco suppression and cigarette blunting
effects will be compared in women and men.
Inclusion Criteria:
- Daily cigarette use of 15 or more cigarettes for at least 2 years
- Screening CO level of or greater than 15 ppm
- Normal or corrected-to-normal vision
- Willing to abstain from tobacco products for 8 or more hours prior to testing
Exclusion Criteria:
- History of chronic health problems or psychiatric conditions
- History of cardiovascular disease, low or high blood pressure, seizures, head
injuries requiring hospital care, peptic ulcer, or diabetes
- Pregnancy (tested by urinalysis)
- Scores greater than 17 on the Beck Depression Inventory
- Lack of a high school degree or GED
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