Maternal Alcohol Reduction Intervention in South Africa [MaRISA]
Mobile Behavioral Intervention to Reduce Maternal Drinking in South Africa
2 other identifiers
interventional
60
1 country
1
Brief Summary
This application proposes to develop and test a technology-based behavioral intervention to address maternal alcohol use in South Africa (SA). SA reports the highest per capita rates of alcohol consumption in the world and has one of the world's highest rates of lifelong disorders called fetal alcohol spectrum disorders (FASD). Prenatal alcohol use is often associated with exposure to gender-based violence, and an increase in gender-based violence due to the uncertainty and economic impact of COVID-19 is of a major concern. Recent evidence also showed that alcohol use during lactation significantly compromises child development in children exposed to alcohol through breastfeeding, and the adverse effect of postpartum alcohol use while breastfeeding was independent of prenatal alcohol exposure. Average breastfeeding duration in SA is beyond 1 year, and over 40% of mothers with and without a history of prenatal drinking report alcohol use while breastfeeding. A community-based behavioral intervention involving case management helps reduce prenatal alcohol use but is labor intensive, challenging the feasibility of widespread implementation in economically disadvantaged communities especially during the COVID-19 pandemic with limited social contact. An efficacious behavioral intervention to reduce alcohol use during pregnancy and lactation needs to be developed that is acceptable and feasible in economically disadvantaged communities, for women with transportation difficulties, or during the COVID-19 pandemic with limited social contact. The proposed intervention will incorporate mobile breathalyzer technology, contingent financial incentives, and text-based health promotion and referrals on gender-based violence, maternal infant health, and psychosocial issues including the impact of COVID-19 in the context of maternal alcohol use. Specific aims are (1) to develop and pretest a technology-based behavioral intervention to help women abstain from alcohol use during pregnancy and lactation via formative qualitative research with women who are pregnant or breastfeeding with a recent history of alcohol use, clinic and community stakeholders, and an established Community Collaborative Board in Cape Metropole, SA, and (2) to examine the acceptability and feasibility of the intervention on alcohol use during pregnancy and lactation by pilot testing the mobile technology-based platform with 60 women who are pregnant or postpartum. Acceptability will be assessed at follow-ups, and feasibility will include recruitment capability, process measures, and intervention outcomes. With the evidence of acceptability and feasibility of the proposed intervention, a large randomized clinical trial will become essential to establish efficacy of the intervention. The potential settings that can remotely incorporate the proposed behavioral intervention include primary care clinics, substance use treatment programs, and publicly funded programs for maternal/infant populations in SA, the United States, and other countries.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2021
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 5, 2021
CompletedFirst Submitted
Initial submission to the registry
March 15, 2022
CompletedFirst Posted
Study publicly available on registry
April 11, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
February 29, 2024
CompletedResults Posted
Study results publicly available
August 23, 2024
CompletedAugust 23, 2024
August 1, 2024
2.3 years
March 15, 2022
June 27, 2024
August 21, 2024
Conditions
Outcome Measures
Primary Outcomes (6)
Urine Ethylglucuronide (EtG) Testing
Number and proportion of participants who were tested negative of alcohol use in urine samples.
Baseline
Urine Ethylglucuronide (EtG) Testing
Number and proportion of participants who were tested negative of alcohol use in urine samples.
6 weeks
Urine Ethylglucuronide (EtG) Testing
Number and proportion of participants who were tested negative of alcohol use in urine samples.
3 months
Self-reported Recent Drinking With Timeline Followback
Self-reported use of daily alcohol by the number of standard drinks based on the definition in South Africa (e.g., 12 g per standard drink). The minimum value is 0 and the maximum has no limit in value. The higher the score is, the worse the outcome would be.
Baseline
Self-reported Recent Drinking With Timeline Followback
Self-reported use of daily alcohol by the number of standard drinks based on the definition in South Africa (e.g., 12 g per standard drink). The minimum value is 0 and the maximum has no limit in value. The higher the score is, the worse the outcome would be.
6 weeks
Self-reported Recent Drinking With Timeline Followback
Self-reported use of daily alcohol by the number of standard drinks based on the definition in South Africa (e.g., 12 g per standard drink). The minimum value is 0 and the maximum has no limit in value. The higher the score is, the worse the outcome would be.
3 months
Study Arms (1)
Mobile incentive-based intervention
EXPERIMENTALContingent incentives on abstinence from alcohol; Text-based health promotion support
Interventions
a technology-based behavioral intervention to address maternal alcohol use with mobile breathalyzer technology or/and urinalysis for biochemical verification of alcohol use, contingent financial incentives on alcohol abstinence, and text-based health promotion.
Eligibility Criteria
You may qualify if:
- Pregnant (≤28 ges wks) or postpartum (≤3 mos)
- Have reported alcohol use during the current pregnancy or lactation
- Positive for alcohol use by urinalysis
- Have their own mobile phone
- Intend to breastfeed for 6 months
- Voluntarily consent
You may not qualify if:
- Participated in focus group discussions or pretesting will not be eligible for pilot testing
- Serious medical problems threatening their current pregnancy or current suicidal thoughts or attempts in the past month
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
South African Medical Research Council
Cape Town, South Africa
Related Publications (1)
Erasmus-Claassen LA, Mpisane N, Petersen Williams P, Browne FA, Myers B, Wechsberg WM, Parry CDH, Taylor SN, Washio Y. Participant experiences with a text message and contingency management intervention for alcohol use during pregnancy and lactation in Cape Town, South Africa. Addict Sci Clin Pract. 2025 Jul 29;20(1):59. doi: 10.1186/s13722-025-00594-7.
PMID: 40734177DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Yukiko Washio
- Organization
- RTI International
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Senior Research Psychologist
Study Record Dates
First Submitted
March 15, 2022
First Posted
April 11, 2022
Study Start
March 5, 2021
Primary Completion
July 1, 2023
Study Completion
February 29, 2024
Last Updated
August 23, 2024
Results First Posted
August 23, 2024
Record last verified: 2024-08
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, CSR
After the main findings are published, we welcome other researchers who want to analyze the data in other ways.