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A Controlled Smoking Cessation Trial and Prospective Cohort Study of Tuberculosis (TB) Treatment Outcomes

Primary Purpose

Smoking Cessation, Tuberculosis

Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Intensive anti-smoking counseling
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Smoking Cessation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

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

Sites / Locations

  • Indus Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Counseling

Standard Care

Arm Description

Intensive anti-smoking counseling

Control group will receive current standard of care.

Outcomes

Primary Outcome Measures

Smoking cessation rate
Smoking cessation rate

Secondary Outcome Measures

negative TB treatment outcome (death, treatment failure, relapse, required prolongation of TB therapy
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.

Full Information

First Posted
July 22, 2014
Last Updated
August 8, 2018
Sponsor
Johns Hopkins University
Collaborators
Global Fund, National Tuberculosis Control Program, Pakistan
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1. Study Identification

Unique Protocol Identification Number
NCT02238405
Brief Title
A Controlled Smoking Cessation Trial and Prospective Cohort Study of Tuberculosis (TB) Treatment Outcomes
Official Title
A Randomized Controlled Smoking Cessation Trial and Prospective Cohort Study of TB Treatment Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
May 25, 2015 (Actual)
Primary Completion Date
December 2017 (Actual)
Study Completion Date
January 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
Global Fund, National Tuberculosis Control Program, Pakistan

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Smoking Cessation, Tuberculosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
350 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Counseling
Arm Type
Experimental
Arm Description
Intensive anti-smoking counseling
Arm Title
Standard Care
Arm Type
No Intervention
Arm Description
Control group will receive current standard of care.
Intervention Type
Other
Intervention Name(s)
Intensive anti-smoking counseling
Intervention Description
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.
Primary Outcome Measure Information:
Title
Smoking cessation rate
Time Frame
1-6 months
Title
Smoking cessation rate
Time Frame
6 months post-TB treatment
Secondary Outcome Measure Information:
Title
negative TB treatment outcome (death, treatment failure, relapse, required prolongation of TB therapy
Description
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.
Time Frame
6 months post-TB treatment

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonathan E Golub, PhD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Indus Hospital
City
Karachi
Country
Pakistan

12. IPD Sharing Statement

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A Controlled Smoking Cessation Trial and Prospective Cohort Study of Tuberculosis (TB) Treatment Outcomes

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