- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04782739
Impact of COVID-19 on Provision and Uptake of Prevention of Mother-to-child Transmission of HIV Services in Zimbabwe
Evaluation of the Impact of the COVID-19 Pandemic on Provision and Uptake of Services for the Prevention of Mother-to-child Transmission of HIV and Syphilis in Zimbabwe
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objectives (i) and (ii) will be met by a retrospective analysis of existing MoHCC data sources, allowing a comprehensive description and evaluation of the effects of the pandemic nationally on pMTCT services and, at a local level, on specialised neonatal care. All public healthcare facilities in Zimbabwe complete monthly returns of aggregate data on numbers of women attending antenatal care (ANC) and having HIV and syphilis testing and treatment during pregnancy, and information on HIV testing, prophylaxis for HIV-exposed infants and treatment of HIV-infected infants. These data are entered onto the DHIS-2 platform. Additionally, the national laboratory database includes data on infant HIV PCR testing.
Data will be extracted from the MoHCC DHIS-2 platform for the 5 years prior to measures taken for lockdown for COVID-19 (which started before any significant community transmission of COVID-19), until at least 6 months after the pandemic in Zimbabwe and corresponding measures end (if possible, depending on the course of the pandemic). National data include returns for 1560 healthcare facilities across 10 provinces. Descriptive analyses will focus on the year prior to lockdown, the period of the pandemic/associated response in Zimbabwe and a minimum of 6 months afterwards; we will describe changes in indicators nationally and by province. The national laboratory data will be used as an independent (unlinked) data source to verify trends in EID. Coverage of ART during pregnancy, infant prophylaxis and ART in infants with HIV will be estimated by combining data from MoHCC returns with Spectrum estimates, as is done routinely. Interrupted time series models will be used to estimate trends in indicators across the three time periods (five years pre-pandemic, during the pandemic, 6-months post pandemic), accounting for seasonal patterns and trends prior to the pandemic.
Objective (ii) will be addressed by analysis of NeoTree data. NeoTree is an application used in the neonatal unit at Harare Children's Hospital which combines data collection by healthcare workers in real-time with interactive decision support and education for improving quality of care.
Objective (iii) will use a qualitative design to provide complementary data to enhance the quantitative results. Longitudinal in-depth individual interviews with pregnant and lactating women, and with healthcare workers will be conducted at the Harare. Participants willing and able to provide informed consent will be purposively recruited from the Family and Child Health unit at Harare Children's Hospital. Participants will take part in two waves of data collection, at study start and after six months.
Objective (v) will draw out key messages from this mixed-methods approach for communication and education. We will design, produce and disseminate educational materials in various media. We will build on existing materials already available in Shona (www.picturinghealth.org) and study findings from objectives (i)-(iv) to develop, pilot and evaluate educational materials for women and families on accessing healthcare safely, and disseminate materials to healthcare workers and policymakers. These will include social media targeted video and short animations in Shona, designed to be easily adaptable to other settings for wider dissemination.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Harare, Zimbabwe
- Kuwadzana Polyclinic
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Harare, Zimbabwe
- Mabvuku Polyclinic
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Group 1:
Anonymous aggregated data will be collated retrospectively for all pregnant women/infants receiving care at all public healthcare facilities in Zimbabwe, from March 2015 to the end of the study
Group 2:
All neonates admitted to Sally Mugabe Central Hospital, from February 2019 to the end of the study
Group 3:
Pregnant/lactating women and community healthcare workers from the Mabvuku and Kuwadzana Polyclinics
Description
Group 1:
Inclusion criteria:
• Anonymous aggregated data will be collated retrospectively for all pregnant women/infants receiving care at all public healthcare facilities in Zimbabwe, from March 2015 to the end of the study
Exclusion criteria:
None
Group 2:
Inclusion criteria:
• All neonates admitted to Sally Mugabe Central Hospital, from February 2019 to the end of the study
Exclusion criteria:
None
Group 3 - Pregnant/lactating women:
Inclusion criteria:
- Accessing antenatal or postnatal services at Mabvuku and Kuwadzana clinics
- Have lived in the Mabvuku and Kuwadzana clinics catchment area during the national lockdown
- Willing and able to give written or audio informed consent for participation.
- Willing to participate in the follow-up study
Exclusion criteria:
None
Group 3 - Community healthcare workers
Inclusion criteria:
- Working and interacting directly with women seeking antenatal or postnatal care services
- Working at the health facility/ community during and prior to the lockdown
- Willing and able to give written or audio informed consent for participation.
Exclusion criteria:
None
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Description of PMTCT service provision and uptake at healthcare facilities
Aggregated data will be collected from all 1560 public healthcare facilities in Zimbabwe on key indicators including antenatal testing and treatment of HIV and syphilis, and management of HIV-exposed and HIV-positive infants.
Data will be collected from March 2015 (5 years prior to the pandemic) to the end of the study, to explore trends over time.
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Descriptive study
|
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Neonatal admissions at Harare Children's Hospital
Individual-level patient data will be collected on all neonates admitted for care at Harare Children's Hospital, including on patient characteristics, clinical status at presentation and outcomes.
Data will be collected from February 2019 to the end of the study, to explore trends over time.
|
Descriptive study
|
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Qualitative study
Qualitative study of 20 pregnant/lactating women accessing routine PMTCT services and 10 community healthcare workers from the Mabvuku and Kuwadzana Polyclinics.
The estimated enrolment of 30 participants given in the study design section above refers to participants from this group only.
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Descriptive study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Proportion of pregnant women seen in antenatal care who are tested for HIV and syphilis
Time Frame: Up to 6 years
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Based on data from Group 1
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Up to 6 years
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Proportion of HIV-positive pregnant women seen in antenatal care who are on antiretroviral therapy
Time Frame: Up to 6 years
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Based on data from Group 1
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Up to 6 years
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Proportion of HIV-exposed infants seen in antenatal care who are tested for HIV by 6 weeks of age
Time Frame: Up to 6 years
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Based on data from Group 1
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Up to 6 years
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Number of HIV-exposed neonates admitted to Sally Mugabe Central Hospital
Time Frame: Up to 2 years
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Based on data from Group 2
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Up to 2 years
|
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Among neonates admitted to Sally Mugabe Central Hospital, number receiving HIV testing and prophylaxis
Time Frame: Up to 2 years
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Based on data from Group 2
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Up to 2 years
|
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Case fatality rate per 1,000 HIV-exposed neonates admitted to Sally Mugabe Central Hospital
Time Frame: Up to 2 years
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Based on data from Group 2
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Up to 2 years
|
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Number of pregnant women who experienced interruptions to PMTCT service delivery
Time Frame: Up to 18 months
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Based on data from Group 3
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Up to 18 months
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Qualitative evaluation of the impact of COVID-19 on provision and uptake of PMTCT services
Time Frame: Up to 18 months
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Based on data from Group 3
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Up to 18 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Mutsa Bwakura-Dangarembizi, University of Zimbabwe Clinical Research Centre
Publications and helpful links
General Publications
- Chappell E, Chimwaza A, Manika N, Wedderburn CJ, Mupambireyi Nenguke Z, Gannon H, Cowan F, Gibb T, Heys M, Fitzgerald F, Phillips A, Chimhuya S, Gibb DM, Ford D, Mushavi A, Bwakura-Dangarembizi M. Impact of the COVID-19 pandemic on the provision and uptake of services for the prevention of mother-to-child transmission of HIV in Zimbabwe. PLOS Glob Public Health. 2023 Aug 14;3(8):e0002296. doi: 10.1371/journal.pgph.0002296. eCollection 2023.
- Gannon H, Chappell E, Ford D, Gibb DM, Chimwaza A, Manika N, Wedderburn CJ, Nenguke ZM, Cowan FM, Gibb T, Phillips A, Mushavi A, Fitzgerald F, Heys M, Chimhuya S, Bwakura-Dangarembizi M. Effects of the COVID-19 pandemic on the outcomes of HIV-exposed neonates: a Zimbabwean tertiary hospital experience. BMC Pediatr. 2024 Jan 5;24(1):16. doi: 10.1186/s12887-023-04473-5.
- Mupambireyi Z, Cowan FM, Chappell E, Chimwaza A, Manika N, Wedderburn CJ, Gannon H, Gibb T, Heys M, Fitzgerald F, Chimhuya S, Gibb D, Ford D, Mushavi A, Bwakura-Dangarembizi M. "Getting pregnant during COVID-19 was a big risk because getting help from the clinic was not easy": COVID-19 experiences of women and healthcare providers in Harare, Zimbabwe. PLOS Glob Public Health. 2024 Jan 8;4(1):e0002317. doi: 10.1371/journal.pgph.0002317. eCollection 2024.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Communicable Diseases
- Sexually Transmitted Diseases
- Pneumonia, Viral
- Pneumonia
- Lung Diseases
- Gram-Negative Bacterial Infections
- Bacterial Infections
- Bacterial Infections and Mycoses
- Sexually Transmitted Diseases, Bacterial
- Spirochaetales Infections
- Treponemal Infections
- Urogenital Diseases
- Genital Diseases
- COVID-19
- Syphilis
Other Study ID Numbers
- MRCZ/A/2682
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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