Study Results
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Basic Information
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COMPLETED
3231 participants
OBSERVATIONAL
2021-07-15
2023-09-30
Brief Summary
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Detailed Description
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Goal The overarching goal of this protocol is to determine the incidence, prevalence, and clinical manifestations of SARS-CoV-2 among patients living with HIV and healthcare workers providing HIV services, and to assess the knowledge, attitudes and practices (KAP) and the impact that COVID-19 has on them and on the healthcare system.
Objectives Primary Objectives
1. To determine the incidence and prevalence of SARS-CoV-2 among unvaccinated PLHIV enrolled in care.
2. To describe the knowledge, attitudes, practices and perceived risks (KAP-P) regarding SARS-CoV-2, prevention, transmission, and management among PLHIV and HCWs providing HIV services.
3. To evaluate the effect of COVID-19 pandemic on retention to HIV care.
Secondary Objectives
1. To determine the clinical, immunologic, and virological outcomes of SARS-CoV-2 infection in PLHIV and HCWs providing HIV care.
2. To describe the perceptions of PLHIV and HCWs providing HIV services regarding the influence that the COVID-19 pandemic has on the delivery of essential services (including HIV/TB care).
3. To measure the fidelity of participating health facilities to the implementation of national COVID-19 guidelines.
4. To describe COVID-19 breakthrough infection among vaccinated PLHIV and health care workers (HCW) providing HIV care.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Cohort 1 (SARS-CoV-2 uninfected)
Participants who test negative on the SARS-CoV-2 rapid test and are not considered at risk of COVID-19 or who have a negative RNA-PCR SARS-CoV-2 test result at baseline.
No interventions assigned to this group
Cohort 2 (SARS-CoV-2 infected)
Participants who test positive on RNA-PCR SARS-CoV-2.
No interventions assigned to this group
Cohort 3 (SARS-CoV-2 exposed)
Participants who have a positive SARS-CoV-2 rapid test result and are not considered to be at risk of active COVID-19 infection or have a negative RNA-PCR SARS-CoV-2 test.
No interventions assigned to this group
Cohort 4 ( Vaccinated)
Participants who declare having received at least one dose of COVID-19 vaccine (verbally or by showing vaccination card) at inclusion (for HCW or PLHIV) or at any follow-up visit (PLHIV) will be followed in this cohort.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Have HIV infection and currently in follow-up care at selected HFs;
* Aged 18 years or older;
* Able and willing to give informed consent;
* Willing to test for exposure to SARS-CoV-2 or COVID-19 infection;
* Willing to be followed and to comply with study visits during the maximum of 15-month study period;
* Does not intend to move from their residence (requiring change of health facility for HIV care) during the study period;
* Willing and able to provide contact information.
2. HCWs offering HIV services
* HCWs (medical doctor, medical officer \["técnico de medicina"\], general nurse \["agente de medicina"\], maternal and child health \[MCH\] nurse, pharmacist, laboratory worker, counselor, ancillary worker \[e.g., archivist, receptionist\], and health volunteers based at the health facility) who are employed full-time and offering HIV services at selected HFs;
* ≥18 years of age ;
* Able and willing to give informed consent;
* Be vaccinated with at least one dose against COVID-19 (verbally or vaccination card));
* Willing to test for exposure to SARS-CoV-2/ COVID-19 infection;
* Willing to be followed and available during the maximum of 15-month study period;
* Does not intend to transfer to another HF during the study period;
* Willing and able to provide contact information.
Exclusion Criteria
* Any clinical or mental condition that, in the investigator's opinion, would preclude provision of informed consent or make study participation unsafe or unethical;
* Any Differentiated Service Delivery where patients have an ART pick-up scheduled less frequently than four times a year (e.g., Community Adherence Support Group \[CASG\] member);
* Patients whose antiretroviral (ARV) drugs are picked up by a confidant during their scheduled appointment.
2. HCWs offering HIV services
* Any clinical or mental conditions that, in the opinion of the investigator or designee, would preclude provision of informed consent or make study participation unsafe or unethical;
* Individuals working in the HF but from the following cadres: drivers, security personnel, and community health workers/volunteers.
18 Years
ALL
Yes
Sponsors
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Centers for Disease Control and Prevention
FED
Instituto Nacional de Saúde, Mozambique
OTHER_GOV
Responsible Party
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Principal Investigators
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Edna Viegas, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
INS-CISPOC
Locations
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INSMozambique
Maputo, , Mozambique
Countries
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References
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De Schacht C, Nhacule E, Belo C, Young PW, Bhatt N, Junior F, Pimentel De Gusmao E, Muquingue H, Muteerwa A, Bila D, Ouenzar MA, Madede T, Cumbane R, Amorim G, Viegas E; COVIV Study Collaborative Group. Measuring the burden of SARS-CoV-2 infection among persons living with HIV and healthcare workers and its impact on service delivery in Mozambique: protocol of a prospective cohort study. BMJ Open. 2023 Jun 6;13(6):e068988. doi: 10.1136/bmjopen-2022-068988.
Other Identifiers
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CGH-MOZ-9/24/20-ef1f9
Identifier Type: -
Identifier Source: org_study_id
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