The Miriam Hospital
Providence, Rhode Island, 02903, United States
NCT Number: NCT00420160
This study compares the effects of a standard smoking cessation treatment, including one-time brief counseling and provision of nicotine patch plus an 8-week moderate intensity exercise program versus the same standard smoking cessation treatment plus equivalent contact control among 60 healthy women. We hypothesize that participants in the smoking cessation plus moderate intensity exercise condition will be more likely to quit smoking than participants in the smoking cessation treament plus contact control condition.
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Notify Me18 year–65 year
Female
Interventional
Phase 2 / Phase 3
Providence, Rhode Island, 02903, United States
This study compares the effects of a standard smoking cessation treatment, including one-time brief counseling and provision of nicotine patch plus an 8-week moderate intensity exercise program versus the same standard smoking cessation treatment plus equivalent contact control among 60 healthy women. A number of techniques will be used to increase compliance with the treatment program, thus more effectively isolating the effects of exercise. These include: (1) a two-week run-in period prior to randomization; (2) use of behavioral contracting prior to participant randomization; and (3) performance of all exercise on-site. Smoking cessation outcomes (continuous abstinence and point prevalence abstinence) will be verified by carbon monoxide and saliva cotinine. Physical activity will be evaluated by attendance at the supervised sessions. We hypothesize that participants in the smoking cessation plus moderate intensity exercise condition will be more likely to quit smoking than participants in the smoking cessation treament plus contact control condition.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Acebutolol Atenolol Carvedilol Metoprolol Nadolol Pindolol Propranolol Timolol
Medical problems:
Psychiatric Problems
REQUIRES MD CONSENT FOR THE SPECIFIC CONDITION
Time frame: post-intervention (8 weeks after baseline)
Time frame: taken one month post-intervention (12 weeks after baseline)
The Miriam Hospital
Other
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