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Intensive Smoking-cessation Intervention Versus Smoking-cessation Advice in Smear-positive Patients With Pulmonary Tuberculosis

Impact of a Package of Intensive Smoking-cessation Interventions Versus Smoking-cessation Advice on Outcomes in Smear-positive Patients With Pulmonary Tuberculosis; a Randomised Controlled Trial (STB_RCT).

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01517022
Enrollment
800
Registered
2012-01-25
Start date
2010-11-30
Completion date
2016-09-30
Last updated
2017-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tuberculosis

Keywords

smoking cessation, early sputum smear conversion

Brief summary

The aim of the study is to determine the impact of a package of smoking-cessation interventions on a composite measure of Tuberculosis (TB) treatment-related outcomes. Given the lack of objective clinical data/evidence about the impact of smoking-cessation on TB-related outcomes, yet subjective expert opinion that smoking cessation is highly likely to be beneficial particularly in patients with TB, this study proposes to determine the impact of an intensive package of smoking-cessation interventions aimed to promote smoking-cessation (counseling plus nicotine replacement therapy, NRT), on patient response to anti-tuberculosis therapy. This is to be compared with the structured counselling for smoking-cessation that is recommended to be routinely provided by health care workers to all patients who are smokers. If the results prove that such a smoking-cessation PI indeed improves outcomes in TB patients, such information would strongly motivate for the institution of more intensive smoking-cessation interventions in TB clinics than is currently being employed for TB patients

Detailed description

No clinical trials have been done to determine if the cessation of smoking has any influence on outcome in tuberculosis patients. In particular, if smoking cessation leads to a higher rate of sputum culture-conversion at 2 months, TB transmission rates should be reduced. Such targeted smoking-cessation intervention may be more successful than general public education strategies in reducing the spread of TB in high-incidence countries Tuberculosis (TB) . The WHO has estimated that approximately a third of the world's population is infected with Mycobacterium tuberculosis, and approximately 2 million die from TB every year. Tobacco smoking, which is the single most preventable cause of death in the world today, appears to be an important risk factor for TB disease and mortality, especially in countries such as India. The smoking-TB association has major public health implications because in many of the developing countries where there is a high prevalence of TB, smoking is also a common practice. Smoking is widespread, with approximately a third of the global population aged 15 years or above being smokers, but has reached epidemic proportions in countries such as India, China and Russia. For example, in India more than half of the rural male population is estimated to smoke and India accounts for 1.85 million TB cases each year. Therefore in India, as for other developing countries, the co-existence of a high TB and smoking burden is a major health concern, and further underscores the importance of promoting smoking cessation to the general public. In India, studies have shown a strong association between tobacco and TB mortality. An estimated third of male TB deaths in India may be due to smoking. However, there is concern that many of the published studies did not adequately control for bias and confounding (that may have caused spurious associations).

Interventions

DRUGnicotine replacement therapy

nicotine replacement therapy 2mg for patients cessation arm for period of 6 weeks

Sponsors

University of Cape Town
CollaboratorOTHER
Sri Venkateswara Institute of Medical Sciences University
CollaboratorOTHER
All India Institute of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* any adult (\> 18 years) * Recently diagnosed (primary TB/Relapse TB) smear-positive TB patient who self-reports to smoke at least 10 whole cigarettes or bidis (rolled tobacco leaf) per day, every day

Exclusion criteria

* patients will be excluded from recruitment to the study if they fall into any one or more of these exclusion categories: * Inability to give consent or \< 18 years * Patients who self-report to smoke less than 10 whole cigarettes/bidis per day * TB patients who have already started anti-tuberculosis therapy for more than 1 week. * Patients with known multidrug-resistant TB (or XDR) (information provided by patient or the information is available in the clinic folder). * Known HIV-positive patients * Contra-indications to NRT (patients with a history of severe cardiovascular disease including arrhythmias, recent myocardial infarction (within the last 6 months), recent cerebrovascular incident (6 months), and/ or history of peripheral vascular disease, phaeochromocytoma, poorly controlled diabetes mellitus, hyperthyroidism, renal/hepatic impairment or gastritis/peptic ulcers). Patients with asthma or depression will also be excluded, as quitting may have an effect on medications used for these conditions. Patients with severe skin disorders (such as psoriasis or eczema) will also be excluded.

Design outcomes

Primary

MeasureTime frameDescription
1. Change in TB Score at second month and sixth monthMeasured at baseline, second month and sixth month.Composite score for objective and subjective improvement measured at baseline, second month and sixth month
Sputum culture conversionMeasured at baseline and second monthSputum culture conversion at second month using solid/liquid culture technique

Secondary

MeasureTime frameDescription
More than 10% weight gain at six monthsSixth monthTo determine rate of weight gain after completion of treatment
Proportion of subjects in each group that have quit smoking at second monthSixth monthTo determine the rate of smoking cessation in the cohort
Sputum smear conversionMeasured at baseline, second week, fourth week, second month and sixth monthsProtocol was amended to access sputum conversion weekly up to second month
Cure, failure and default rateAt sixth monthTo determine cure, failure and default rate in the cohort
Treatment completionSix months for new cases and eight months for re-treatment cases following regimen 2
Mortality at sixth monthSixth monthTo determine number of mortality at the end of follow-up

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026