HIV Clinical Trial
— MONARCHOfficial title:
Optimizing the Delivery of Maternal and Child Health Services to Strengthen the Primary Health Care System in Rural South Africa
Verified date | December 2015 |
Source | University of KwaZulu |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study evaluates the impact of a quality improvement (QI) intervention on maternal and child healthcare services in seven primary healthcare (PHC) clinics, in a rural setting of KwaZulu-Natal, South Africa.
Status | Completed |
Enrollment | 3172 |
Est. completion date | January 30, 2017 |
Est. primary completion date | January 26, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 50 Years |
Eligibility |
Inclusion Criteria: - Currently postpartum: immediately post delivery OR 3-6 days postpartum OR 6 weeks postpartum; AND - Lives in Africa Centre Demographic Surveillance Area (DSA); AND/OR - Attended antenatal care (ANC) or postnatal care (PNC) in study intervention clinics Exclusion Criteria: - Below 18 years of age; - Not postpartum; - Does not live within Africa Centre DSA; AND - Did not attend ANC or PNC at study intervention clinics |
Country | Name | City | State |
---|---|---|---|
South Africa | Africa Centre for Population Health | Mtubatuba | KwaZulu-Natal |
Lead Sponsor | Collaborator |
---|---|
University of KwaZulu |
South Africa,
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Kim YM, Banda J, Kanjipite W, Sarkar S, Bazant E, Hiner C, Tholandi M, Reinhardt S, Njobvu PD, Kols A, Benavides B. Improving performance of Zambia Defence Force antiretroviral therapy providers: evaluation of a standards-based approach. Glob Health Sci Pract. 2013 Aug 14;1(2):213-27. doi: 10.9745/GHSP-D-13-00053. eCollection 2013 Aug. — View Citation
Maman D, Huerga H, Mukui I et al (2015). Most Breastfeeding Women with High Viral Load Are Still Undiagnosed in Sub-Saharan Africa. Conference on Retroviruses and Opportunistic Infections. Abstract number 32. Available at: http://www.croiconference.org/sessions/most-breastfeeding-women-high-viral-load-are-still-undiagnosed-sub-saharan-africa
Massyn N, Day C, Peer N et al eds (2013/14). District Health Barometer Durban: Health Systems Trust; October 2014.
Mutiso P, Simba M, Towett R et al (2014). Effective monitoring of HIV prevention: re-testing HIV-negative clients. 20th International AIDS Conference, Melbourne Australia. Abstract number WEPE178. Available at: http://pag.aids2014.org/abstracts.aspx?aid=7817
Mwaniki MK, Vaid S, Chome IM, Amolo D, Tawfik Y; Kwale Improvement Coaches. Improving service uptake and quality of care of integrated maternal health services: the Kenya Kwale District improvement collaborative. BMC Health Serv Res. 2014 Sep 21;14:416. doi: 10.1186/1472-6963-14-416. — View Citation
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Webster PD, Sibanyoni M, Malekutu D, Mate KS, Venter WD, Barker PM, Moleko W. Using quality improvement to accelerate highly active antiretroviral treatment coverage in South Africa. BMJ Qual Saf. 2012 Apr;21(4):315-24. doi: 10.1136/bmjqs-2011-000381. — View Citation
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of HIV-infected pregnant women who are on ART and have received an HIV VL test | At study mid-point and study end (approximately 20 months) | ||
Primary | Proportion of women who are HIV-uninfected at first ANC HIV test with a repeat antenatal HIV test | At study mid-point and study end (approximately 20 months) | ||
Secondary | Proportion of HIV-infected pregnant women who have HIV virologic suppression | At study mid-point and study end (approximately 20 months) | ||
Secondary | Uptake of exclusive breastfeeding | At study mid-point and study end (approximately 20 months) | ||
Secondary | Uptake of contraception | At study mid-point and study end (approximately 20 months) | ||
Secondary | Proportion of HIV-infected women initiated on ART during pregnancy/breastfeeding (PMTCT) | At study mid-point and study end (approximately 20 months) | ||
Secondary | Number of participants with knowledge of early infant feeding | At study mid-point and study end (approximately 20 months) | ||
Secondary | Number of participants with knowledge of available contraception | At study mid-point and study end (approximately 20 months) | ||
Secondary | Number of participants with knowledge of HIV | At study mid-point and study end (approximately 20 months) | ||
Secondary | Subjective experience: patient satisfaction with services | At study mid-point and study end (approximately 20 months) | ||
Secondary | Subjective experience: provider job satisfaction and motivation | At study mid-point and study end (approximately 20 months) | ||
Secondary | Proportion of infant HIV PCR positivity among HIV-exposed infants (HEI) | At study mid-point and study end (approximately 20 months) | ||
Secondary | Proportion of HEI receiving nevirapine prophylaxis | At study mid-point and study end (approximately 20 months) | ||
Secondary | Proportion of participants enrolled at delivery attending 6-week postnatal visit | As a measure of retention in care at 6 weeks postpartum | At study mid-point and study end (approximately 20 months) |
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