Smoking Cessation Interventions for People Living With HIV in Nairobi, Kenya
- Conditions
- HIVSmoking Cessation
- Interventions
- Registration Number
- NCT03342027
- Lead Sponsor
- University of Maryland, Baltimore
- Brief Summary
The proposed study will use a factorial design to evaluate the most promising and accessible behavioral and pharmacologic treatments aimed at achieving maximal efficacy for smoking cessation among people living with HIV who smoke. The study will randomize 300 participants people living with HIV , who smoke and who are receiving care in HIV clinics affiliated with the Center for International Health, Education, and Biosecurity in Nairobi, Kenya to one of the following 4 conditions: (1) bupropion + Positively Smoke Free (an 8 session tailored behavioral intervention for people living with HIV smokers); (2) bupropion + Standard of Care (brief advice to quit); (3) Placebo + Positively Smoke Free; and (4) Placebo + Standard of Care.
- Detailed Description
The proposed study will use a factorial design to evaluate the most promising and accessible behavioral and pharmacologic treatments aimed at achieving maximal efficacy for smoking cessation among people living with HIV who smoke. The will randomize 300 participants people living with HIV, who smoke and who are receiving care at HIV clinics affiliated with the Center for International Health, Education, and Biosecurity in Nairobi, Kenya to one of the following 4 conditions: (1) bupropion + Positively Smoke Free (an 8 session tailored behavioral intervention for people living with HIV smokers); (2) bupropion + Standard of Care (brief advice to quit); (3) Placebo + Positively Smoke Free; and (4) Placebo + Standard of Care. The study will use a factorial design as it is a highly efficient method of assessing multiple treatments in a single trial with the possibility of saving both time and resources. All participants will be assessed at baseline,12 weeks and 36 weeks with the main outcome being 7-day abstinence (defined as self-reported no smoking in the past 7 days + CO\<7 ppm).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 300
Not provided
- Has a history of seizure disorder or bulimia nervosa
- Recent use of Bupropion (by participant report in the past 3 months)
- Previous allergic reaction/hypersensitivity to Bupropion (by participant report ever in lifetime)
- Pregnant, nursing, or becoming pregnant during the study (pregnancy test)
- Current use of any medication that would interfere with the protocol in the opinion of a medically accountable Physician
- Known plans to re-locate or travel away from the study site for more than two consecutive months during the study period.
- Expected survival of less than 6 months
- Meets criteria for dementia by scoring below 10 on the Hopkins HIV Dementia Scale.
- The study physician believes that the individual is not medially stable enough to participate in the study. This exclusion will be based on a review of the individual's past medical history and current medical status.
- Based on screening, not meeting criteria for moderate or severe substance disorder as established by the MINI International Neuropsychiatric Interview.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- FACTORIAL
- Arm && Interventions
Group Intervention Description Bupropion + Positively Smoke Free Positively smoke free Positively smoke free-- an 8 session tailored behavioral treatment for smoking cessation bupropion--used for smoking cessation Bupropion + Standard of Care Brief advice to quit smoking Standard of Care--brief advice to quit provided in a standardized format bupropion--used for smoking cessation Bupropion + Standard of Care Bupropion Standard of Care--brief advice to quit provided in a standardized format bupropion--used for smoking cessation Placebo + Positively Smoke Free Positively smoke free Placebo--matched to bupropion Positively smoke free-- an 8 session tailored behavioral treatment for smoking cessation Placebo + Standard of Care. Brief advice to quit smoking Placebo--matched to bupropion Standard of Care--brief advice to quit provided in a standardized format Bupropion + Positively Smoke Free Bupropion Positively smoke free-- an 8 session tailored behavioral treatment for smoking cessation bupropion--used for smoking cessation
- Primary Outcome Measures
Name Time Method 7-day Abstinence Up to 36 Weeks defined as self-reported no smoking in the past 7 days + CO\<7 ppm
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Center for International Health, Education, and Biosecurity (CIHEB)
🇰🇪Kilimani, Nairobi, Kenya