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BCG to Reduce Absenteeism Among Health Care Workers During the COVID-19 Pandemic (EDCTP)

Primary Purpose

Covid19, Morbidity, Absenteeism

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
BCG-Denmark
Saline
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Covid19 focused on measuring Innate immune training, Non-specific effects of BCG, Heterologous effects

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • health care worker (physician, nurse, or other) based at one of the research hospitals.
  • age ≥18 years

Exclusion Criteria:

  • known allergy to (components of) BCG or serious adverse events to prior BCG administration;
  • known previous, active or latent infection with Mycobacterium tuberculosis or other mycobacterial species
  • fever (>38 C) within past 24 hours;
  • previous confirmed COVID-19 (positive test - PCR or antibody);
  • suspicion of active viral or bacterial infection
  • severely immunocompromised subjects
  • self-reported HIV infection
  • self-reported pregnancy;
  • active solid or non-solid malignancy or lymphoma within the prior two years;
  • contraindications for live attenuated vaccine administration.
  • not having a mobile phone.

Sites / Locations

  • Bandim Health Project
  • Manhiça Health Research Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

BCG-Denmark

Control

Arm Description

Participants that are randomized in the active arm will receive an adult 0.1 ml dose of BCG vaccine (BCG-Denmark, AJ Vaccines) in the skin covering the right upper deltoid muscle. Each 0.1 ml vaccine contains between 200000 to 800000 colony forming units of the live attenuated strain of Mycobacterium bovis (BCG), Danish strain 1331.

Placebo will be 0.1 ml sterile 0.9 % NaCl, which has a similar color and appearance as the resuspended BCG vaccine.

Outcomes

Primary Outcome Measures

Days of unplanned absenteeism due to illness
Unplanned absenteeism is defined by being absent from work due to causes other than holidays, parental leave, and other planned leaves, family assistance (including mourning leave) and quarantine measures.

Secondary Outcome Measures

Days of unplanned absenteeism due to documented COVID-19
Unplanned absenteeism is defined by being absent from work due to causes other than holidays, parental leave, and other planned leaves, family assistance (including mourning leave) and quarantine measures.
Cumulative incidence of hospital admissions due to illness (minus accidents).
Hospital admissions involves staying at a hospital for at least one night or more for medical reasons. It includes admissions to hospital wards and overnight stays in emergency departments.
Death
Whether the participant died during follow-up

Full Information

First Posted
November 22, 2020
Last Updated
November 2, 2022
Sponsor
University of Southern Denmark
Collaborators
Institute of Hygiene and Tropical Medicine, NOVA University, Lisbon, Portugal, University of Cape Verde, Praia, Cape Verde, National Institute of Public Health of Cape Verde, Praia, Cape Verde, Centro de Investigacao em Saude de Manhica, European and Developing Countries Clinical Trials Partnership (EDCTP), Bandim Health Project, Bissau, Guinea-Bissau
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1. Study Identification

Unique Protocol Identification Number
NCT04641858
Brief Title
BCG to Reduce Absenteeism Among Health Care Workers During the COVID-19 Pandemic
Acronym
EDCTP
Official Title
BCG Vaccine to Reduce Unplanned Absenteeism Due to Illness of Health Care Workers During the COVID-19 Pandemic. A Multi-center Randomised Controlled Trial (BCG-COVID-RCT)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
December 3, 2020 (Actual)
Primary Completion Date
July 13, 2022 (Actual)
Study Completion Date
July 13, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Southern Denmark
Collaborators
Institute of Hygiene and Tropical Medicine, NOVA University, Lisbon, Portugal, University of Cape Verde, Praia, Cape Verde, National Institute of Public Health of Cape Verde, Praia, Cape Verde, Centro de Investigacao em Saude de Manhica, European and Developing Countries Clinical Trials Partnership (EDCTP), Bandim Health Project, Bissau, Guinea-Bissau

4. Oversight

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

5. Study Description

Brief Summary
The COVID-19 pandemic challenges available hospital capacity. Strategies to protect health care workers (HCW) are desperately needed. Bacille Calmette- Guérin (BCG) has protective non-specific effects against other infections; a plausible immunological mechanism has been identified in terms of "trained innate immunity". The primary objective of the study is to evaluate whether BCG can reduce unplanned absenteeism due to illness among HCW during the COVID-19 pandemic. Secondary objectives are to reduce the number of HCW that are infected with COVID-19, reduce hospital admissions for HCW and to improve the capacity for clinical research. Design: Single-blind, parallel-group placebo-controlled multi-centre block randomized trial including a total of 1050 HCW. The study sites will be the Manhiça hospital in Mozambique, Central Hospital Dr. Agostinho Neto and Central Hospital Dr. Baptista de Sousa in Cape Verde and Hospital Nacional Simão Mendes and other hospitals in the capital Bissau in Guinea-Bissau. Population: HCW (nurses/physicians/others) ≥18 years. Intervention: Block randomization 1:1 to intradermal standard dose (0.1 ml) of BCG vaccine or placebo (saline). Endpoints: Primary: Days of unplanned absenteeism due to illness. Secondary: Days of absenteeism because of documented COVID-19; cumulative incidence of infectious disease hospitalizations. Follow-up: mobile phone interviews every second week, regarding symptoms, absenteeism and causes, COVID-19 testing (if done) and their results. Perspectives: If BCG can reduce HCW absenteeism it has global implications. The intervention can quickly be scaled up all over the world.
Detailed Description
The main hypothesis for this study is that BCG vaccination of HCW reduces unplanned absenteeism due to illness by 20%. Trial design Single-blind, parallel-group placebo-controlled adaptive multicentre trial, with block-randomisation 1:1 (treatment:placebo) in blocks of 20 within strata defined by gender (male/female) and occupational group (doctors/ nurses/other) to an intradermal standard 0.1 ml dose of BCG vaccine or placebo (saline) including a total of 1050 HCW (BCG arm and placebo arm). Study population: Health Care Workers defined as a person who delivers care and services to the sick and ailing either directly as doctors and nurses or indirectly as aides, helpers, laboratory technicians, or even medical waste handlers. Intervention: The intervention will consist of the administration of an intradermal injection of a standard 0.1 ml adult dose of attenuated Mycobacterium bovis BCG (Bacillus Calmette-Guerin), Danish strain 1331, 2-8 × 10*5 CFU or the placebo comparator: intradermal standard 0.1 ml saline solution (NaCl 0.9%). Both BCG and saline solution will be injected in the skin over the upper deltoid muscle. Blinding: The BCG vaccine will be administered by study physicians/nurses, who are not blinded but also not involved in the data collection. Participants, data collectors and data entry clerks will be blinded to the treatment allocation. In case of serious adverse events, the participant can be unblinded after consultation with the investigator or the vaccinating physician/nurse. When the study has ended, all participants will receive information about the intervention that they received. Follow-up: Follow-up will last for 6 months (182 days). Every second week, participants will be contacted over telephone and interviewed for symptoms and absenteeism from work. By the end of follow-up, participants will be invited for another POC test for COVID-19 serology. Sample size: The sample size was calculated on the basis of the primary hypothesis. A total of 1050 HCW randomized with an estimated loss to follow-up of 5%, and a mean number of days off work due to illness in the control group of 5 days (SD=5) over a 6-month period will demonstrate a reduction among BCG vaccinated of 20% for a mean absence of 4 days (80% power and alpha 0.05). The estimated loss to follow-up (5%) was based on past telephone-based surveys conducted in Mozambique and Bissau.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, Morbidity, Absenteeism
Keywords
Innate immune training, Non-specific effects of BCG, Heterologous effects

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Multi-center randomized placebo-controlled trial
Masking
ParticipantOutcomes Assessor
Masking Description
Participants will be blinded to treatment. The physicians administering the BCG vaccine or placebo will not be blinded. Those assessing outcomes will be blinded to the randomization allocation. In case of serious adverse events, the participant can be unblinded after consultation with the coordinating PI or sponsor.
Allocation
Randomized
Enrollment
668 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BCG-Denmark
Arm Type
Active Comparator
Arm Description
Participants that are randomized in the active arm will receive an adult 0.1 ml dose of BCG vaccine (BCG-Denmark, AJ Vaccines) in the skin covering the right upper deltoid muscle. Each 0.1 ml vaccine contains between 200000 to 800000 colony forming units of the live attenuated strain of Mycobacterium bovis (BCG), Danish strain 1331.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Placebo will be 0.1 ml sterile 0.9 % NaCl, which has a similar color and appearance as the resuspended BCG vaccine.
Intervention Type
Biological
Intervention Name(s)
BCG-Denmark
Intervention Description
Participants randomized to receive BCG will receive one 0.1 ml dose of Mycobacterium bovis BCG live attenuated BCG-Denmark vaccine (AJ Vaccines, Copenhagen, Denmark) by intradermal injection in the left deltoid region.
Intervention Type
Biological
Intervention Name(s)
Saline
Intervention Description
Participants randomized to the control group will receive one 0.1 ml dose sterile 0.9 % NaCl by intradermal injection in the right deltoid region.
Primary Outcome Measure Information:
Title
Days of unplanned absenteeism due to illness
Description
Unplanned absenteeism is defined by being absent from work due to causes other than holidays, parental leave, and other planned leaves, family assistance (including mourning leave) and quarantine measures.
Time Frame
6 months after inclusion
Secondary Outcome Measure Information:
Title
Days of unplanned absenteeism due to documented COVID-19
Description
Unplanned absenteeism is defined by being absent from work due to causes other than holidays, parental leave, and other planned leaves, family assistance (including mourning leave) and quarantine measures.
Time Frame
6 months after inclusion
Title
Cumulative incidence of hospital admissions due to illness (minus accidents).
Description
Hospital admissions involves staying at a hospital for at least one night or more for medical reasons. It includes admissions to hospital wards and overnight stays in emergency departments.
Time Frame
6 months after inclusion
Title
Death
Description
Whether the participant died during follow-up
Time Frame
6 months after inclusion
Other Pre-specified Outcome Measures:
Title
Hospitalisation for COVID-19
Description
Refers to the number of nights of hospitalisation due to COVID-19
Time Frame
6 months after inclusion
Title
Hospitalisation besides COVID-19
Description
Refers to the number of nights of hospitalisation due to other reasons besides COVID-19
Time Frame
6 months after inclusion
Title
Time to hospitalisation
Description
Time, in days, from enrolment to first night of hospitalisation
Time Frame
6 months after inclusion
Title
Time to absenteeism
Description
Time, in days, from enrolment to first day absent from work due to ill-health and disease
Time Frame
6 months after inclusion
Title
Time to COVID-19 absenteeism
Description
Refers to the number of days since enrolment to first day absent from work due to suspected COVID-19
Time Frame
6 months after inclusion
Title
COVID-19 infection
Description
Describes if the participant is positive for SARS-CoV2 or has had COVID-19
Time Frame
6 months after inclusion
Title
Time to COVID-19
Description
Time, in days, from enrolment to positive test for SARS-CoV2
Time Frame
6 months after inclusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: health care worker (physician, nurse, or other) based at one of the research hospitals. age ≥18 years Exclusion Criteria: known allergy to (components of) BCG or serious adverse events to prior BCG administration; known previous, active or latent infection with Mycobacterium tuberculosis or other mycobacterial species fever (>38 C) within past 24 hours; previous confirmed COVID-19 (positive test - PCR or antibody); suspicion of active viral or bacterial infection severely immunocompromised subjects self-reported HIV infection self-reported pregnancy; active solid or non-solid malignancy or lymphoma within the prior two years; contraindications for live attenuated vaccine administration. not having a mobile phone.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine Stabell Benn, Professor
Organizational Affiliation
University of Southern Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bandim Health Project
City
Bissau
State/Province
SAB
ZIP/Postal Code
1004
Country
Guinea-Bissau
Facility Name
Manhiça Health Research Centre
City
Manhiça
State/Province
Maputo
ZIP/Postal Code
1929
Country
Mozambique

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Non-identifiable individual data can be shared on the basis of a data sharing proposal sent to professor Inês Fronteira ifronteira@ihmt.unl.pt
IPD Sharing Time Frame
When follow-up has been completed and the dataset have been closed.
IPD Sharing Access Criteria
Non-identifiable individual data can be shared on the basis of a data sharing proposal sent to ifronteira@ihmt.unl.pt
Citations:
PubMed Identifier
25232810
Citation
Aaby P, Kollmann TR, Benn CS. Nonspecific effects of neonatal and infant vaccination: public-health, immunological and conceptual challenges. Nat Immunol. 2014 Oct;15(10):895-9. doi: 10.1038/ni.2961.
Results Reference
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PubMed Identifier
31449870
Citation
Aaby P, Benn CS. Developing the concept of beneficial non-specific effect of live vaccines with epidemiological studies. Clin Microbiol Infect. 2019 Dec;25(12):1459-1467. doi: 10.1016/j.cmi.2019.08.011. Epub 2019 Aug 23.
Results Reference
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PubMed Identifier
32645296
Citation
Benn CS, Fisker AB, Rieckmann A, Sorup S, Aaby P. Vaccinology: time to change the paradigm? Lancet Infect Dis. 2020 Oct;20(10):e274-e283. doi: 10.1016/S1473-3099(19)30742-X. Epub 2020 Jul 6.
Results Reference
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PubMed Identifier
21673035
Citation
Aaby P, Roth A, Ravn H, Napirna BM, Rodrigues A, Lisse IM, Stensballe L, Diness BR, Lausch KR, Lund N, Biering-Sorensen S, Whittle H, Benn CS. Randomized trial of BCG vaccination at birth to low-birth-weight children: beneficial nonspecific effects in the neonatal period? J Infect Dis. 2011 Jul 15;204(2):245-52. doi: 10.1093/infdis/jir240.
Results Reference
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PubMed Identifier
29579158
Citation
Biering-Sorensen S, Aaby P, Lund N, Monteiro I, Jensen KJ, Eriksen HB, Schaltz-Buchholzer F, Jorgensen ASP, Rodrigues A, Fisker AB, Benn CS. Early BCG-Denmark and Neonatal Mortality Among Infants Weighing <2500 g: A Randomized Controlled Trial. Clin Infect Dis. 2017 Oct 1;65(7):1183-1190. doi: 10.1093/cid/cix525.
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PubMed Identifier
27737834
Citation
Higgins JP, Soares-Weiser K, Lopez-Lopez JA, Kakourou A, Chaplin K, Christensen H, Martin NK, Sterne JA, Reingold AL. Association of BCG, DTP, and measles containing vaccines with childhood mortality: systematic review. BMJ. 2016 Oct 13;355:i5170. doi: 10.1136/bmj.i5170. Erratum In: BMJ. 2017 Mar 8;356:j1241.
Results Reference
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PubMed Identifier
27380797
Citation
Rieckmann A, Villumsen M, Sorup S, Haugaard LK, Ravn H, Roth A, Baker JL, Benn CS, Aaby P. Vaccinations against smallpox and tuberculosis are associated with better long-term survival: a Danish case-cohort study 1971-2010. Int J Epidemiol. 2017 Apr 1;46(2):695-705. doi: 10.1093/ije/dyw120.
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Nemes E, Geldenhuys H, Rozot V, Rutkowski KT, Ratangee F, Bilek N, Mabwe S, Makhethe L, Erasmus M, Toefy A, Mulenga H, Hanekom WA, Self SG, Bekker LG, Ryall R, Gurunathan S, DiazGranados CA, Andersen P, Kromann I, Evans T, Ellis RD, Landry B, Hokey DA, Hopkins R, Ginsberg AM, Scriba TJ, Hatherill M; C-040-404 Study Team. Prevention of M. tuberculosis Infection with H4:IC31 Vaccine or BCG Revaccination. N Engl J Med. 2018 Jul 12;379(2):138-149. doi: 10.1056/NEJMoa1714021.
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BCG to Reduce Absenteeism Among Health Care Workers During the COVID-19 Pandemic

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