Project Details
Description
Background: Worldwide estimates suggest that people living with HIV/AIDS (PLWH) smoke at nearly
three times the rate of the general population. Smoking among PLWH living in sub-Saharan Africa is
associated with gender (male>female), with living in an urban slum community, and perhaps most
importantly with illicit substance use. Although precise prevalence estimates of tobacco use among PLWH in
Kenya are lacking, recent data collected from a large, well established methadone maintenance program in
Nairobi found the prevalence of smoking among PLWH with opiate use disorders was 100%. This compares
to 7.7-9.1% in the Kenyan general population. Many interventions are effective in helping smokers in the
general population quit. To what degree these data translate to PLWH in lower-middle income countries that
may have greater challenges with health infrastructure, resources and medication access, is not clear.
Approach: Our 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
PLWH who smoke. We propose to randomize 300 participants PLWH, who smoke and who are receiving
care in a methadone maintenance program in Nairobi, Kenya to one of the following 4 conditions: (1)
bupropioin + Positively Smoke Free (an 8 session tailored behavioral intervention for PLWH smokers); (2)
bupropion + Standard of Care (brief advice to quit); (3) Placebo + Positively Smoke Free; and (4) Placebo +
Standard of Care. We plan to 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. We plan to conduct the
study in a methadone maintenance clinic for several reasons. First, smoking rates are shockingly high in this
setting, and the need for effective tobacco treatment is enormous. Second, there is great synergy in providing
behavioral and pharmacological treatment for smoking cessation interventions to clients who are already
receiving a pharmacological intervention (i.e., methadone) with concomitant substance use counseling. Third,
people in methadone maintenance come regularly to receive treatment which is likely to enhance smoking
cessation treatment follow-up and completion. 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
Status | Active |
---|---|
Effective start/end date | 9/5/18 → 8/31/23 |
Funding
- National Cancer Institute: $604,482.00
- National Cancer Institute: $629,333.00
- National Cancer Institute: $624,460.00
- National Cancer Institute: $99,999.00
- National Cancer Institute: $634,879.00
Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.