COV19HWVE_GE: COVID-19 Vaccine Effectiveness Among Health Workers in Georgia

Sponsor
National Center for Disease control and Public Health (Other)
Overall Status
Recruiting
CT.gov ID
NCT04868448
Collaborator
World Health Organization (Other)
1,600
6
16.4
266.7
16.3

Study Details

Study Description

Brief Summary

This is a prospective one-year cohort study of hospital-based health workers in Georgia to evaluate the effectiveness of COVID-19 vaccine in preventing laboratory-confirmed SARS-CoV-2 infection and COVID-19 disease.

Condition or Disease Intervention/Treatment Phase
  • Biological: Covid-19 vaccines

Detailed Description

Many critical questions remain about the effectiveness of COVID-19 vaccines in real-world settings. These questions can only be answered in post-introduction vaccine effectiveness studies.

This is a prospective one-year cohort study of hospital-based health workers in Georgia to evaluate the effectiveness of COVID-19 vaccine in preventing laboratory-confirmed SARS-CoV-2 infection and COVID-19 disease. Health Workers (HWs) are the target population in this study because they have been prioritized to be the first group to receive the vaccine in Georgia and offer an early opportunity to evaluate the vaccine in a population in which it is critical that an effective vaccine be deployed.

HWs should be enrolled after the study protocol is approved by the local ethical review committee. All HWs eligible to be vaccinated with COVID-19 vaccine can be enrolled in the study, including those who intend to get vaccinated, those who do not plan on getting vaccinated, and those who are not sure. For HWs who have already been vaccinated at enrolment, priority will be given to those who have received their first COVID vaccine no more than 4 days prior to the date of enrolment. The target enrolment is 1600 participants.

At enrolment, study participants will complete a baseline enrolment survey about demographics, clinical comorbidities, and work and community-related behaviors related to infection risk, and recent symptoms. In addition, a baseline serology will be collected from participants at enrolment.

For study participants who have not received their first COVID-19 vaccine at enrolment but receive their first vaccine 14 days or more after enrolment, an additional blood sample will be collected. In addition, a brief symptom questionnaire about recent symptoms will be administered.

During the course of the study, participants will be actively followed for suspected COVID-19 infection. Participants will be asked to complete weekly symptom questionnaires to screen for clinically significant COVID-19. Participants who meet a suspected case definition, defined according to the Georgian national case definition should provide a respiratory sample which will be collected by trained HW. Respiratory specimens will be tested for SARS-CoV-2 by RT-PCR.

All or subset of positive samples from study participants will undergo genetic sequencing, resources permitting.

Finally, after 3, 6, 9 and 12 months of the study, as resources permit, serology will be collected from participants. Serology will be tested for antibodies to SARS-CoV-2 by tests for vaccine-induced antibodies and antibodies that result from natural infection.

Vaccine effectiveness should be analysed as described in the analysis section below.

In addition to the final analysis at the end of the one-year period, interim quarterly (every three months) analyses will be undertaken.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1600 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Cohort Study to Measure COVID-19 Vaccine Effectiveness Among Health Workers in Georgia
Actual Study Start Date :
Mar 20, 2021
Anticipated Primary Completion Date :
Aug 1, 2022
Anticipated Study Completion Date :
Aug 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Vaccinated participants

Participants who received 1or 2 doses of the Covid-19 vaccines

Biological: Covid-19 vaccines
Observation of individuals who received one or more doses of covid-19 vaccines.

Unvaccinated participants

Participants who have not received any dose of the Covid-19 vaccines

Outcome Measures

Primary Outcome Measures

  1. Covid-19 vaccine effectiveness [12 months]

    any SARS-CoV-2 laboratory confirmation by RT-PCR in an asymptomatic, or symptomatic patient

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

All HWs eligible to receive the COVID-19 vaccination according to the national guidelines of Ministry of Health (MoH).

  • HWs working at Batumi Republican Clinical Hospital, Vakhtang Bochorishvili Clinic, Academician N. Kipshidze Central University Clinic, Bokeria Tbilisi Referral Hospital, Caucasus Medical Centre, and Infectious Diseases and AIDS Center.

  • HWs who have already been vaccinated with a single dose of vaccine against COVID-19 as part of the early COVID-19 vaccine rollout can be included.

Exclusion Criteria:
  • HWs who are not eligible for COVID-19 vaccination or have a contraindication to vaccination should not participate in the study.

  • HWs who do not work at above mentioned hospitals

  • HWs under 18 years of age.

  • HWs who have already been vaccinated with two doses of vaccine against COVID-19 before enrolment

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Batumi Republican Clinical Hospital Batumi Ajara Georgia
2 The Bokeria Tbilisi Referral Hospital Tbilisi Georgia 0145
3 Academician N. Kipshidze Central University Clinic Tbilisi Georgia 0160
4 The Bochorishvili Clinic Tbilisi Georgia 0160
5 The Infectious Diseases and AIDS Center Tbilisi Georgia 0160
6 The Caucasus Medical Centre Tbilisi Georgia 0186

Sponsors and Collaborators

  • National Center for Disease control and Public Health
  • World Health Organization

Investigators

  • Principal Investigator: Khatuna C Zakhashvili, MD, National Center for Disease control and Public Health

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr.Lia Sanodze, Principal Investigator, National Center for Disease control and Public Health
ClinicalTrials.gov Identifier:
NCT04868448
Other Study ID Numbers:
  • CERC.0097B
First Posted:
May 3, 2021
Last Update Posted:
May 3, 2021
Last Verified:
Apr 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr.Lia Sanodze, Principal Investigator, National Center for Disease control and Public Health
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 3, 2021