Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | Nicotine replacement therapy - Transdermal nicotine patch | Medication selection will be determined based on individual participant preferences, medical history, and contraindications. |
| DRUG | Nicotine replacement therapy - Nicotine gum | Medication selection will be determined based on individual participant preferences, medical history, and contraindications. |
| DRUG | Nicotine replacement therapy - Nicotine lozenge | Medication selection will be determined based on individual participant preferences, medical history, and contraindications. |
| DRUG | Bupropion | Medication selection will be determined based on individual participant preferences, medical history, and contraindications. |
| DRUG | Varenicline | Medication selection will be determined based on individual participant preferences, medical history, and contraindications. |
| DRUG | Combination pharmacotherapy - Transdermal nicotine patch + nicotine gum | Medication selection will be determined based on individual participant preferences, medical history, and contraindications. |
| DRUG | Combination pharmacotherapy - Transdermal nicotine patch + nicotine lozenge | Medication selection will be determined based on individual participant preferences, medical history, and contraindications. |
| DRUG | Combination pharmacotherapy - Transdermal nicotine patch + bupropion | Medication selection will be determined based on individual participant preferences, medical history, and contraindications. |
| BEHAVIORAL | Tobacco quitline referral | Participants 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. |
| BEHAVIORAL | Tailored behavioral intervention | Participants will receive a standard six session cognitive behavioral intervention for smoking cessation combined with supplemental treatment modules based on individual need and preference. |
| BEHAVIORAL | Alcohol use risk reduction | Participants engaging in risky alcohol use may receive this six-session telephone-based behavioral intervention for reducing alcohol use. |
| BEHAVIORAL | Behavioral activation for depressive symptoms | Participants with elevated depressive symptoms may receive this six-session telephone-based behavioral activation intervention. |
| BEHAVIORAL | Behavioral management of postcessation weight gain | Participants 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.