Evaluation of a Home-based Community Health Worker Program in Rural Eastern Cape, South Africa

Depression Clinical Trial

Official title:

A Non-randomized Comparative Cohort Study Evaluating a Home-based Community Health Worker Program in the Rural Eastern Cape Province of South Africa

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03517878
• Other study ID #: N14/03/019
• Status: Completed
• Start date: August 11, 2014
• Est. completion date: June 1, 2018

Study information

• Verified date: October 2018
• Source: University of California, Los Angeles
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of this early Phase 2 comparison trial is to evaluate the impact of community health worker (CHW) home visitors on pregnant women and their children in a rural setting in the rural Eastern Cape of South Africa. The intervention provided by the CHWs targets underweight children, mothers living with HIV (MLH), mothers using alcohol, and depressed mothers with the goal of supporting pregnant women to improve birth outcomes, decrease the number of children born with a low birthweight, and develop child caretaking skills over time. UCLA has identified and matched four areas surrounding primary health care clinics: two intervention areas in which this CHW program has been running for one year, and two control areas without the program. Mothers in the research area are followed for one year after giving birth.

Description:

Inequalities in the quality and accessibility of healthcare between urban centers and rural areas is a global challenge that is particularly stark for low and middle-income countries (LMIC). Maternal and child health (MCH) in rural South Africa is negatively impacted by large distances, poor infrastructure, and a shortage of healthcare workers at clinics and hospitals.

Home visiting has been repeatedly demonstrated efficacious in addressing some of these challenges and improving MCH outcomes, including when delivered by CHW in LMIC. However, there is limited research on the effectiveness of implementing these types of programs in rural areas.

The investigators have shown that with training, supervision, and accountability, CHW home visits are effective in improving MCH over the first five years of life. These results were observed in a successful randomized controlled trial 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 health challenges concurrently. The visits significantly improved MCH outcomes over five years. Based on these results, this comprehensive CHW home visiting program served as one model for re-engineering primary health care to include 65,000 paraprofessionals providing home-based care in South Africa.

This early phase two comparison trial examines whether the same comprehensive CHW home visiting program can be effectively implemented in a deeply rural area of the Eastern Cape in South Africa. Two matched cohorts of women and their children, one in areas where the comprehensive CHW program has been active for one year and one in areas without the program, will be followed from pregnancy through the first 12 months after giving birth. 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, and 12 months later. The primary outcomes are a combined measures of maternal and child health including maternal HIV testing, depression, and alcohol use, as well as the child's nutrition, physical growth, development, and healthcare and a measure of how MLH comply with tasks for PMTCT.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1490
• Est. completion date: June 1, 2018
• Est. primary completion date: June 1, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Pregnant women who are or become mothers living in the catchment area at the time of recruitment

• Women not identified as psychotic or delusional based on the interviewer's judgment

• Women able to provide informed consent

Exclusion Criteria:

• Inability to give informed consent

• Inability to converse with the interviewer or the CHW

• Miscarriage or stillbirth

• Death of the infant

• Death of the mother

Related Conditions & MeSH terms

• Alcohol Drinking
• Alcohol Use Disorder
• Alcohol; Harmful Use
• Birth Weight
• Birth Weight Less Than 10Th Percentile
• Child Development
• Child Malnutrition
• Child Nutrition Disorders
• Depression
• Depressive Symptoms
• Disease
• HIV Infections
• HIV/AIDS
• Malnutrition
• Nutrition Disorders
• Stunting

Intervention

Behavioral:
• Comprehensive CHW Program
The comprehensive CHW Cohort will receive home visits from CHWs recruited, trained, and supervised by the Philani organization. Philani has a 30-year history of non-stigmatizing home-based support for women and children in Cape Town. The organization has been operating their comprehensive CHW program in the rural Eastern Cape since 2010; however, in the research areas, CHWs have only been active for one year prior to initiation of the study. Philani recruits CHWs that are "positive peer deviants" to serve as role models in the community. The CHWs then receive training, materials, and skills to address major community health challenges of HIV, TB, malnutrition, alcohol use, and depression. The CHWs also receive ongoing monitoring and supervision as well as support for difficult cases.

Locations

Country	Name	City	State
South Africa	Zithulele Hospital	Mqanduli	Eastern Cape
South Africa	Stellenbosch University	Stellenbosch

Sponsors (4)

Lead Sponsor	Collaborator
University of California, Los Angeles	Philani Maternal Child Health and Nutrition Project, The ELMA Foundation, University of Stellenbosch

Country where clinical trial is conducted

South Africa, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Composite outcome: Number of significantly improved child and maternal outcomes	Out of 11 variables, we run 1000 simulations on the distribution of 0 and 1. The investigators total number of outcomes (each scored as 0=not present or 1=present) and determine if the Comprehensive CHW Cohort sum is significantly greater than expected based on the Control Cohort.; For Mothers: Breastfeeding; No alcohol in pregnancy; Not depressed; Adhere to medical regimens; For all mothers: -4 antenatal care visits; For HIV+ mothers: Test for HIV; Take ARV; Give infant NVP and bactrim; infant PCR; exclusive breastfeeding; For Children: Not low birth weight; Growth in height; Growth in weight; Hospitalizations; Developmental milestones; Vaccinations; Child support grant; Harwood JM, Weiss RE, Comulada WS. Beyond the Primary Endpoint Paradigm: A Test of Intervention Effect in HIV Behavioral Intervention Trials with Numerous Correlated Outcomes. Prevention Science. 2017 Jul 1;18(5):526-33.	12 months
Secondary	Breastfeed for three months	Mothers are asked at the 6 month and 12 month follow up "How long after your baby's birth did you stop breastfeeding your baby completely?"	6 months, 12 months
Secondary	Breastfeed for six months	Mothers are asked at the 6 month and 12 month follow up "How long after your baby's birth did you stop breastfeeding your baby completely?"	6 months, 12 months
Secondary	No alcohol after learning that the participant was pregnant	At the birth interview mothers are asked "Have you ever used alcohol during this pregnancy?" and follows up with "Did you continue to drink alcohol after you knew you were pregnant?"	Birth
Secondary	Attend 4 antenatal care visits	At the birth interview antenatal care cards are inspected and mothers are asked "How many antenatal care visits did you attend?"	Birth
Secondary	Not depressed, EPDS below 13	EPDS is asked after birth, 6 months after birth, and at 12 months after birth.	Birth, 6 months, 12 months
Secondary	Infant was not low birth weight	Birth weight is recorded from child's road to health card and baby is weighed by data collector shortly after birth (this value is used when road to health card is not available).	Birth
Secondary	Growth in height-for-age (above -2SD)	Child height/length is recorded shortly after birth, at 6 months, and at 12 months. Values are compared to WHO norms and turned into a Z score.	Birth, 6 months, 12 months
Secondary	Growth in weight-for-age (above -2SD)	Child weight is recorded shortly after birth, at 6 months, and at 12 months. Values are compared to WHO norms and turned into a Z score.	Birth, 6 months, 12 months
Secondary	Number of Hospitalizations	At 6 months and 12 months after birth mothers are asked "During the past 3 months, have you taken the child to the hospital for any reason?" and "How many times have you taken the child to the hospital?"	6 months, 12 months
Secondary	WHO developmental scale measures at 50th percentile	WHO measures of child development are used and children are compared to the mean level of achievement for their age. Fussy or sleepy children may be unable to be evaluated.	12 months
Secondary	Vaccinations up to date	Data collectors examine the child's road to health card to determine if all immunizations are up to date and which ones are missing. A photo is taken of this page for confirmation.	12 months
Secondary	Has Child Support Grant	Mothers are asked "Does the child get a child support grant?"	12 months
Secondary	Mothers test for HIV during pregnancy	Data collectors look for any evidence on the antenatal card of an HIV test during pregnancy. If not, or if card is unavailable, check with the mother if she has previously tested positive for HIV or ask "Did you have a test for HIV during this pregnancy?"	Birth
Secondary	MLH take ARV during pregnancy	Mothers are asked "When did you start taking ARVs?" and antenatal cards and health cards are examined for evidence of ARV prescription and start date.	12 months
Secondary	Give infant NVP and Bactrim	Mothers are asked "Did you get Nevarapine syrup for your baby around the time of birth?"; "Are you currently using nevirapine syrup for the baby?" and "Are you currently still giving your child bactrim?"	6 months
Secondary	PCR testing at 6 weeks	Mothers are asked "Has you child been tested for HIV yet?" and "Do you know what the result of your child's HIV test (PCR) is?" Data collectors independently confirm this information on the child's road to health card to determine how many times (if at all) the child has been tested for HIV?	12 months
Secondary	6 months exclusive breastfeeding	Mothers are asked "How soon after birth did you give your child something else in addition to breastmilk?" In addition, mothers are asked to provide a 24 hour, 1 months, and 3 month dietary recall.	6 months

External Links

•   Philani Website
•   Zithuele Research Website