Smoking Cessation, Tuberculosis
Conditions
Brief summary
The primary focus of this intervention trial is to understand the effect of quitting smoking on TB treatment outcomes. The investigators will compare a cessation strategy based on guidelines recommended by the World Health Organization (WHO) and the International Union against Tuberculosis and Lung Disease (IUTLD). This is currently not utilized in TB directly observed therapy (DOT) clinics in Pakistan. The investigators study will provide comprehensive data towards understanding the effectiveness of these strategies for TB patients who smoke in Pakistan, and most importantly, on the effect of quitting smoking on TB treatment outcomes. These findings will guide development of effective smoking cessation strategies in a region with high prevalence of TB and increasing tobacco use.
Interventions
OTHERIntensive anti-smoking counseling
Study participants randomized to the intervention arm will receive intensive cessation support outside of the TB clinic setting, from a health worker trained in cessation counseling, during the course of their TB treatment. Behavioral elements will consist of follow up using unscheduled drop in or phone sessions, motivational interviewing, and counseling tailored to the needs and circumstances of the patient. Patients who are current smokers and are ready to commit to quit smoking will be supported to stop completely. Recent smokers will supported for having quit, and the counselor will discuss coping strategies to maintain abstinence.
Sponsors
Global Fund
National Tuberculosis Control Program, Pakistan
Johns Hopkins University
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Males, ≥18 years of age * diagnosed with pulmonary TB * self-reported current smokers, or smoker within 6 months * anticipated to be attending the TB treatment clinic for at least 6 months * be willing to set a quit date within 2 weeks after baseline assessment * agree to participate
Exclusion criteria
* less than 18 years of age * quit for more than 6 months * extra-pulmonary TB * unable/unwilling to provide written consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Smoking cessation rate | 1-6 months |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| negative TB treatment outcome (death, treatment failure, relapse, required prolongation of TB therapy | 6 months post-TB treatment | To assess differences in TB treatment outcomes between smokers and quitters, all patients enrolled in the intervention trial will be included in analyses of a composite negative outcome variable, defined as a composite endpoint of poor clinical response to TB treatment including death, treatment failure, relapse, and/or requirement for prolongation of TB therapy. Risk of a negative treatment outcome will be compared between the following 3 groups: 1) TB patients who were current smokers and quit smoking for 6 months of follow-up; 2) TB patients who were recent smokers and stayed quit for 6 months of follow-up; and, 3) TB patients who are never smokers. |
Countries
Pakistan
Outcome results
None listed