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

Primary Purpose

Tuberculosis

Status
Completed
Phase
Phase 3
Locations
India
Study Type
Interventional
Intervention
nicotine replacement therapy
Sponsored by
All India Institute of Medical Sciences, New Delhi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Tuberculosis focused on measuring smoking cessation, early sputum smear conversion

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • All India Institute of Medical Sciences, Ansari Nagar

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control arm

Intervention arm

Arm Description

Control arm patients will receive pre designed pamphlets and structured conselling for smoking cessation by trained counsellors along with routine DOTS treatment

Cessation arm patients will receive pre designed pamphlets and structured conselling for smoking cessation by trained counsellors along and nicotine replacement therapy(NRT) and routine DOTS treatment

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Sputum smear conversion
Protocol was amended to access sputum conversion weekly up to second month
Mortality at sixth month
To determine number of mortality at the end of follow-up
More than 10% weight gain at six months
To determine rate of weight gain after completion of treatment
Proportion of subjects in each group that have quit smoking at second month
To determine the rate of smoking cessation in the cohort
Treatment completion
Cure, failure and default rate
To determine cure, failure and default rate in the cohort

Full Information

First Posted
June 23, 2011
Last Updated
October 12, 2017
Sponsor
All India Institute of Medical Sciences, New Delhi
Collaborators
University of Cape Town, Sri Venkateswara Institute of Medical Sciences University
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1. Study Identification

Unique Protocol Identification Number
NCT01517022
Brief Title
Intensive Smoking-cessation Intervention Versus Smoking-cessation Advice in Smear-positive Patients With Pulmonary Tuberculosis
Official Title
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).
Study Type
Interventional

2. Study Status

Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
November 2010 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
September 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
All India Institute of Medical Sciences, New Delhi
Collaborators
University of Cape Town, Sri Venkateswara Institute of Medical Sciences University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
smoking cessation, early sputum smear conversion

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
800 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Control arm patients will receive pre designed pamphlets and structured conselling for smoking cessation by trained counsellors along with routine DOTS treatment
Arm Title
Intervention arm
Arm Type
Active Comparator
Arm Description
Cessation arm patients will receive pre designed pamphlets and structured conselling for smoking cessation by trained counsellors along and nicotine replacement therapy(NRT) and routine DOTS treatment
Intervention Type
Drug
Intervention Name(s)
nicotine replacement therapy
Other Intervention Name(s)
Nicogum 2mg Cipla pharmaceuticals
Intervention Description
nicotine replacement therapy 2mg for patients cessation arm for period of 6 weeks
Primary Outcome Measure Information:
Title
1. Change in TB Score at second month and sixth month
Description
Composite score for objective and subjective improvement measured at baseline, second month and sixth month
Time Frame
Measured at baseline, second month and sixth month.
Title
Sputum culture conversion
Description
Sputum culture conversion at second month using solid/liquid culture technique
Time Frame
Measured at baseline and second month
Secondary Outcome Measure Information:
Title
Sputum smear conversion
Description
Protocol was amended to access sputum conversion weekly up to second month
Time Frame
Measured at baseline, second week, fourth week, second month and sixth months
Title
Mortality at sixth month
Description
To determine number of mortality at the end of follow-up
Time Frame
Sixth month
Title
More than 10% weight gain at six months
Description
To determine rate of weight gain after completion of treatment
Time Frame
Sixth month
Title
Proportion of subjects in each group that have quit smoking at second month
Description
To determine the rate of smoking cessation in the cohort
Time Frame
Sixth month
Title
Treatment completion
Time Frame
Six months for new cases and eight months for re-treatment cases following regimen 2
Title
Cure, failure and default rate
Description
To determine cure, failure and default rate in the cohort
Time Frame
At sixth month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Surendra K Sharma, MD, Ph.D.
Organizational Affiliation
AIIMS, New Delhi
Official's Role
Principal Investigator
Facility Information:
Facility Name
All India Institute of Medical Sciences, Ansari Nagar
City
New Delhi
ZIP/Postal Code
110029
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
34611902
Citation
Hartmann-Boyce J, Theodoulou A, Farley A, Hajek P, Lycett D, Jones LL, Kudlek L, Heath L, Hajizadeh A, Schenkels M, Aveyard P. Interventions for preventing weight gain after smoking cessation. Cochrane Database Syst Rev. 2021 Oct 6;10(10):CD006219. doi: 10.1002/14651858.CD006219.pub4.
Results Reference
derived

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

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