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Airborne Preventive Measures to Reduce New TB Infections in Household Contacts (TBMask)

Primary Purpose

Tuberculosis, Pulmonary, Household Contacts, Tuberculosis

Status
Recruiting
Phase
Not Applicable
Locations
Chile
Study Type
Interventional
Intervention
Respiratory bundle
Sponsored by
Pontificia Universidad Catolica de Chile
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Tuberculosis, Pulmonary

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • all household contacts of a new case of pulmonary TB (smear, culture or PCR positive) newly diagnosed at each clinic.

Exclusion Criteria:

  • household contacts found to have co-prevalent active TB at enrolment
  • household contacts planning to leave the house at the time of enrolment
  • household contacts of index cases having already initiated TB treatment for > 48h
  • household contacts of index cases that are currently hospitalized

Sites / Locations

  • Pontificia Universidad Católica de ChileRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Respiratory Bundle Group

Standard of care

Arm Description

The intervention consists of a bundle of measures for respiratory transmission prevention that will be provided during the first 2 weeks of TB treatment of index case.

Under current national guidelines, no systematic recommendation regarding respiratory protection is given for household contacts of TB cases.

Outcomes

Primary Outcome Measures

Participation rate
To document the proportion of TB cases and household contacts who agree to participate as measured by enrollment.
Study compliance
To document participants compliance with the respiratory bundle as measured by a previously validated adherence questionnaire.
Completion rate
The number of participants assessable at end of follow-up.
Acceptability of the intervention
Focus group evaluation (participants and TB nurses perspectives, qualitative outcome).

Secondary Outcome Measures

New tuberculosis infections
The number of participants converting from a negative to a positive latent TB test at follow-up.

Full Information

First Posted
May 12, 2021
Last Updated
September 27, 2022
Sponsor
Pontificia Universidad Catolica de Chile
Collaborators
Fondo Nacional de Desarrollo Científico y Tecnológico, Chile, Agencia Nacional de Investigación y Desarrollo
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1. Study Identification

Unique Protocol Identification Number
NCT04938596
Brief Title
Airborne Preventive Measures to Reduce New TB Infections in Household Contacts
Acronym
TBMask
Official Title
Strengthening of Airborne Preventive Measures Inside Households of Pulmonary TB Cases as a Tool to Reduce New Infections in Close Contacts. A Pilot, Controlled, Pre-post Study.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 4, 2021 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
September 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pontificia Universidad Catolica de Chile
Collaborators
Fondo Nacional de Desarrollo Científico y Tecnológico, Chile, Agencia Nacional de Investigación y Desarrollo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Tuberculosis (TB) is currently one of the top 10 causes of death worldwide and the leading cause of death from a single infectious agent (ranking above HIV/AIDS). The investigators hypothesize that reducing respiratory exposure within the household, during the first weeks of TB treatment initiation of the index case, can reduce new TB infections in close contacts. For this purpose, a pilot, controlled, pre-post study will be set up, to evaluate the feasibility of implementing a bundle of respiratory precautions to all household contacts of new pulmonary TB cases, compared to standard of care, in primary health care in a high TB incidence area in Santiago, Chile.
Detailed Description
Tuberculosis (TB) is currently one of the top 10 causes of death worldwide and the leading cause of death from a single infectious agent (ranking above HIV/AIDS). In 2018, an estimated 10 million people fell ill with TB worldwide, and more than 1.4 million people died from it, making eradication of this disease in the next decades highly unlikely unless new interventions are discovered. Mycobacterium tuberculosis (Mtb) transmission mainly occurs when patients affected by laryngeal or pulmonary TB cough upon others and the mycobacteria are spread in airborne droplets nuclei smaller than 5 μm that are subsequently inhaled by close contacts. Although chemoprophylaxis once a new TB infection is detected is an effective strategy to reduce the risk of contacts developing active TB, it does not prevent Mtb acquisition; it only reduces the risk of developing active TB once infected. Currently, the large majority of international guidelines recommend strict measures to reduce airborne transmission in hospitalized patients with pulmonary TB, with a minimum of 2 weeks of effective TB therapy to consider a patient no longer infectious and discontinue respiratory isolation in healthcare settings. On the contrary, in the community, no special recommendations regarding protection of household contacts are specified, assuming that most of them are already infected and that the TB index case will stop infecting very quickly under antimicrobial treatment. However, several studies show that median time to sputum Mtb culture conversion under effective treatment takes 5-7 weeks, raising the potential for continued transmission even despite effective treatment. Furthermore, a previous study has shown that in Santiago, Chile, 55% of household contacts of TB cases have no evidence of TB infection at the time of diagnosis of the index case - as categorized by negative latent TB testing - yet under close follow-up, up to 21% of these show new evidence of having acquired the infection based on latent TB test conversion after 12 weeks of follow-up. The investigators hypothesize that reducing respiratory exposure within the household, during the first weeks of TB treatment initiation of the index case, can reduce new TB infections in close contacts. For this purpose, a pilot, controlled, pre-post study will be done to evaluate the feasibility of implementing a bundle of respiratory precautions to all household contacts of new pulmonary TB cases, compared to standard of care, in primary care in a high TB incidence area in Santiago. The respiratory bundle in the intervention arm will be implemented as soon as a new pulmonary TB case is diagnosed, will last 2 weeks and, will include: (a) provision of N95 masks and strong recommendation of use to all household contacts and the index case when sharing a room together, (b) recommendation to index case to sleep in a room alone, with the door closed and avoid sharing room with others, (c) promotion of strategies to improve house ventilation; and (d) education about TB transmission. The investigators expect to show that this trial is feasible to proceed with a larger, definitive cluster randomized controlled trial that will evaluate the intervention effectiveness in reducing the incidence of new TB infections in household contacts. The results of this study will help to answer a critical research gap in TB infection control and prevention and, it will provide a key contribution to future policies regarding TB control and elimination worldwide. Furthermore, in the new global context of rising infectious agents of pandemic risk, this work may have an additional potential relevance with respect to the use, acceptability and transmission prevention potential of a respiratory bundle in the household setting regarding other respiratory pathogens such as SARS-Cov-2.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis, Pulmonary, Household Contacts, Tuberculosis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Pre-post controlled study. Two different health care areas of Santiago (and their corresponding TB clinics) will be allocated to control or intervention arm; after a baseline pre-intervention period.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Respiratory Bundle Group
Arm Type
Experimental
Arm Description
The intervention consists of a bundle of measures for respiratory transmission prevention that will be provided during the first 2 weeks of TB treatment of index case.
Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
Under current national guidelines, no systematic recommendation regarding respiratory protection is given for household contacts of TB cases.
Intervention Type
Combination Product
Intervention Name(s)
Respiratory bundle
Intervention Description
Provision of N95 masks and strong recommendation of use to all household contacts and the index case when sharing a room together, for 2 weeks Recommendation to index case to sleep in a room alone, with the door closed and avoid sharing room with others during 2 weeks Promotion of strategies to improve house ventilation during 2 weeks Provision of a TB leaflet and nurse education about TB transmission.
Primary Outcome Measure Information:
Title
Participation rate
Description
To document the proportion of TB cases and household contacts who agree to participate as measured by enrollment.
Time Frame
2 weeks
Title
Study compliance
Description
To document participants compliance with the respiratory bundle as measured by a previously validated adherence questionnaire.
Time Frame
2 weeks
Title
Completion rate
Description
The number of participants assessable at end of follow-up.
Time Frame
12 weeks
Title
Acceptability of the intervention
Description
Focus group evaluation (participants and TB nurses perspectives, qualitative outcome).
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
New tuberculosis infections
Description
The number of participants converting from a negative to a positive latent TB test at follow-up.
Time Frame
12 weeks

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: all household contacts of a new case of pulmonary TB (smear, culture or PCR positive) newly diagnosed at each clinic. Exclusion Criteria: household contacts found to have co-prevalent active TB at enrolment household contacts planning to leave the house at the time of enrolment household contacts of index cases having already initiated TB treatment for > 48h household contacts of index cases that are currently hospitalized
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Romina Seguel, RN
Phone
+56223543508
Email
rjseguel@uc.cl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
María Elvira Balcells, MD; MSc
Organizational Affiliation
School of Medicine. Pontificia Universidad Católica de Chile.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pontificia Universidad Católica de Chile
City
Santiago
Country
Chile
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Airborne Preventive Measures to Reduce New TB Infections in Household Contacts

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