Clinical Trials Directory

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UnknownNCT01892813

Dissemination of a Tailored Tobacco Quitline for Rural Veteran Smokers

Tailored Tobacco Intervention

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
411 (actual)
Sponsor
Mark Vander Weg · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Accepted

Summary

The project is designed to examine the effectiveness of strategies to increase access to treatment for tobacco use and dependence among rural Veteran smokers. In addition, it will examine whether tailored treatment that is designed to address common comorbid conditions that are related to cigarette smoking enhances success with quitting relative to enhanced standard of care. The investigators hypothesize that participants assigned to the tailored tobacco cessation intervention will report greater cessation rates at six months. The investigators also anticipate more favorable outcomes on measures of depressive symptoms, alcohol use, and body weight.

Conditions

Interventions

TypeNameDescription
DRUGNicotine replacement therapy - Transdermal nicotine patchMedication selection will be determined based on individual participant preferences, medical history, and contraindications.
DRUGNicotine replacement therapy - Nicotine gumMedication selection will be determined based on individual participant preferences, medical history, and contraindications.
DRUGNicotine replacement therapy - Nicotine lozengeMedication selection will be determined based on individual participant preferences, medical history, and contraindications.
DRUGBupropionMedication selection will be determined based on individual participant preferences, medical history, and contraindications.
DRUGVareniclineMedication selection will be determined based on individual participant preferences, medical history, and contraindications.
DRUGCombination pharmacotherapy - Transdermal nicotine patch + nicotine gumMedication selection will be determined based on individual participant preferences, medical history, and contraindications.
DRUGCombination pharmacotherapy - Transdermal nicotine patch + nicotine lozengeMedication selection will be determined based on individual participant preferences, medical history, and contraindications.
DRUGCombination pharmacotherapy - Transdermal nicotine patch + bupropionMedication selection will be determined based on individual participant preferences, medical history, and contraindications.
BEHAVIORALTobacco quitline referralParticipants assigned to this condition will receive a referral to their state tobacco quitline. The specific behavioral treatment that is provided will differ slightly depending upon the services available through the participant's state of residence.
BEHAVIORALTailored behavioral interventionParticipants will receive a standard six session cognitive behavioral intervention for smoking cessation combined with supplemental treatment modules based on individual need and preference.
BEHAVIORALAlcohol use risk reductionParticipants engaging in risky alcohol use may receive this six-session telephone-based behavioral intervention for reducing alcohol use.
BEHAVIORALBehavioral activation for depressive symptomsParticipants with elevated depressive symptoms may receive this six-session telephone-based behavioral activation intervention.
BEHAVIORALBehavioral management of postcessation weight gainParticipants with concerns about gaining weight after quitting smoking may receive this six-session telephone-based behavioral self-management intervention designed to help attenuate post-cessation weight gain.

Timeline

Start date
2013-07-01
Primary completion
2018-01-01
Completion
2018-01-01
First posted
2013-07-04
Last updated
2017-07-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01892813. Inclusion in this directory is not an endorsement.