Improving South African Government Workers' Capacities to Deliver HIV Interventions
Primary Purpose
HIV, Partner Violence, Malnutrition
Status
Unknown status
Phase
Phase 2
Locations
South Africa
Study Type
Interventional
Intervention
Accountable Condition
Control Condition
Sponsored by
About this trial
This is an interventional prevention trial for HIV focused on measuring Pregnancy, Home Healthcare Visits, Community Health Workers, Infants
Eligibility Criteria
Inclusion Criteria:
- Mothers living in the catchment area
- Mothers not identified as psychotic or delusional based on the interviewer's judgment
- Mothers able to provide informed consent
Exclusion Criteria:
- Inability to give informed consent
- Inability to converse with the interviewer or the CHW
- Death of the mother or infant.
Sites / Locations
- Stellenbosch University
- Zithulele Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Accountable Condition- 8 clinics
Control Condition- 8 clinics
Arm Description
In the Accountable Condition, the intervention includes mothers who will receive home visits from government-funded CHW who will be trained once under Philani and receive ongoing monitoring and supervision.
The Control Condition will include mothers who receive home visits from government-funded CHW who will be trained once under Philani and receive supervision and monitoring consistent with local government practices.
Outcomes
Primary Outcome Measures
Number of significantly improved child and maternal outcomes
Out of 10 variables, the investigators total number of outcomes that are significantly better in the Accountable Condition compared to the Control Condition. The variables are for mothers and children:
For Mothers:
Adhere to medical regimens
Breastfeed for six months (mixed ok)
No alcohol after learning that the participant was pregnant
Mental health, EPDS
For Children:
Growth in height (<-2SD)
Growth in weight (<-2SD)
Number of Hospitalizations
WHO developmental scale measure in normal range
In normal range of CBCL
In normal range on the Bayley
Secondary Outcome Measures
Number of significantly improved child and maternal outcomes for HIV positive mothers
Out of 9 variables, the investigators total the number of outcomes that are significantly better in the Accountable Condition compared to the Control Condition for HIV positive mothers. The variables are:
ARV 6 weeks before birth
NVP at birth
Cipro for child
TB testing
AZT for child
PCR testing at 6 weeks
Get the results of PCR testing
One feeding method for 6 months
Breastfeed solely for 6 months.
Full Information
NCT ID
NCT02957799
First Posted
October 26, 2016
Last Updated
October 5, 2021
Sponsor
University of California, Los Angeles
Collaborators
National Institute of Mental Health (NIMH), University of Stellenbosch
1. Study Identification
Unique Protocol Identification Number
NCT02957799
Brief Title
Improving South African Government Workers' Capacities to Deliver HIV Interventions
Official Title
A Randomized Controlled Trial to Improve the South African Government's Community Health Workers' Capacities to Deliver Evidence-based Interventions for Optimizing HIV Outcomes and Reducing Its Comorbidities
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
October 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
Collaborators
National Institute of Mental Health (NIMH), University of Stellenbosch
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 purpose of this study is to address the United States Office of AIDS Research highest priorities: improving the workforce, reducing health disparities, and addressing HIV comorbidities. UCLA will randomize the government-funded community health workers (CHW) from 16 clinics in matched rural areas in the Eastern Cape in South Africa to either: 1) the Accountable Condition (AC) in which additional monitoring and accountability systems that Philani routinely uses are implemented or 2) a Control Condition (CC), of initial Philani training, but ongoing supervision and monitoring consistent with local government practices.
Detailed Description
Each dollar invested in maternal, child health (MCH) yields a nine-fold benefit. Home visiting has been repeatedly demonstrated efficacious in improving MCH outcomes, including when delivered by CHW in low and middle income countries (LMIC). However, when home visiting programs are scaled, they are not effective. Africa has particular challenges with broad implementation of effective interventions often associated with the poorly trained and poorly monitored health personnel, in this case, CHW who are perinatal home visitors.
The investigators have shown that with training, supervision, and accountability, CHW home visits are effective in a successful randomized controlled trial (RCT) conducted in peri-urban townships in Cape Town, South Africa. CHW were trained to address HIV, alcohol, and malnutrition among all pregnant women in a neighborhood - to avoid stigma and to address multiple challenges concurrently. The visits significantly improved maternal and child outcomes over three years. Based on these results, the Philani Intervention Model served as one model for re-engineering primary health care for 65,000 CHW in South Africa. The Mthatha Provincial Government has agreed for the Philani Program to train, monitor, and supervise their already-hired CHW. This RCT will evaluate whether routinely implementing training and monitoring CHW behavior and MCH outcomes with mobile phones, and providing data-informed supervision, will result in CHW becoming more effective. Stellenbosch University interviewers will independently assess outcomes of each mother at pregnancy, and of the mothers and infants within two weeks of post-birth, 6 months, 15 months, and 24 months later. The primary outcome will be maternal HIV/TB testing, linkage to care, treatment adherence and retention in medical regimens, depression, and parenting; and her child's physical growth, cognitive functioning, and behavior adjustment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Partner Violence, Malnutrition, Alcohol Use/Abuse, Depression
Keywords
Pregnancy, Home Healthcare Visits, Community Health Workers, Infants
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
840 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Accountable Condition- 8 clinics
Arm Type
Experimental
Arm Description
In the Accountable Condition, the intervention includes mothers who will receive home visits from government-funded CHW who will be trained once under Philani and receive ongoing monitoring and supervision.
Arm Title
Control Condition- 8 clinics
Arm Type
Experimental
Arm Description
The Control Condition will include mothers who receive home visits from government-funded CHW who will be trained once under Philani and receive supervision and monitoring consistent with local government practices.
Intervention Type
Behavioral
Intervention Name(s)
Accountable Condition
Intervention Description
Mothers will receive home visits by government-funded CHW who will be trained under Philani as well as receive ongoing monitoring and supervision. CHW will monitor mother's health and linkage to care; CHW will refer all mothers to local clinics for HIV, blood sugar, and pregnancy testing. CHW will also have a mobile phone to record information at each visit. CHW will log their home visits each day, rate the content and skills addressed on the mobile phone, weigh children, and report outcome achievements (e.g., receiving the child grant, immunizations, breastfeeding, and retention/ adherence to HIV care). The CHW in this arm will receive data-informed supervision. CHW will be monitored weekly with review of contact logs, recorded outcomes, and random site visits by supervising in-service training on a monthly basis. The Accountable Condition will last for two years (until the child is 24 months old).
Intervention Type
Behavioral
Intervention Name(s)
Control Condition
Intervention Description
Mothers will receive home visits by government-funded CHW who will be trained under Philani as well as receive supervision and monitoring consistent with local government practices. CHW will monitor mother's health and linkage to care. CHW will refer all mothers to local clinics for HIV, blood sugar, and pregnancy testing. The Control Condition will last for two years (until the child is 24 months old).
Primary Outcome Measure Information:
Title
Number of significantly improved child and maternal outcomes
Description
Out of 10 variables, the investigators total number of outcomes that are significantly better in the Accountable Condition compared to the Control Condition. The variables are for mothers and children:
For Mothers:
Adhere to medical regimens
Breastfeed for six months (mixed ok)
No alcohol after learning that the participant was pregnant
Mental health, EPDS
For Children:
Growth in height (<-2SD)
Growth in weight (<-2SD)
Number of Hospitalizations
WHO developmental scale measure in normal range
In normal range of CBCL
In normal range on the Bayley
Time Frame
2 Years
Secondary Outcome Measure Information:
Title
Number of significantly improved child and maternal outcomes for HIV positive mothers
Description
Out of 9 variables, the investigators total the number of outcomes that are significantly better in the Accountable Condition compared to the Control Condition for HIV positive mothers. The variables are:
ARV 6 weeks before birth
NVP at birth
Cipro for child
TB testing
AZT for child
PCR testing at 6 weeks
Get the results of PCR testing
One feeding method for 6 months
Breastfeed solely for 6 months.
Time Frame
2 Years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Mothers living in the catchment area
Mothers not identified as psychotic or delusional based on the interviewer's judgment
Mothers able to provide informed consent
Exclusion Criteria:
Inability to give informed consent
Inability to converse with the interviewer or the CHW
Death of the mother or infant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mary Jane Rotheram-Borus
Organizational Affiliation
Study Principal Investigator Department of Psychiatry & Biobehavioral Sciences, Semel Institute, UCLA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stellenbosch University
City
Stellenbosch
Country
South Africa
Facility Name
Zithulele Hospital
City
Zithulele
Country
South Africa
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
At the conclusion of this study we have a plan to de-identify the data and to make it available to other researchers.
Citations:
PubMed Identifier
28784142
Citation
Rotheram-Borus MJ, Le Roux K, Le Roux IM, Christodoulou J, Laurenzi C, Mbewu N, Tomlinson M. To evaluate if increased supervision and support of South African Government health workers' home visits improves maternal and child outcomes: study protocol for a randomized control trial. Trials. 2017 Aug 7;18(1):368. doi: 10.1186/s13063-017-2074-5.
Results Reference
derived
Learn more about this trial
Improving South African Government Workers' Capacities to Deliver HIV Interventions
We'll reach out to this number within 24 hrs