Maternal Alcohol Reduction Intervention in South Africa [MaRISA]

NCT ID: NCT05319977

Last Updated: 2024-08-23

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-05

Study Completion Date

2024-02-29

Brief Summary

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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.

Detailed Description

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Conditions

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Maternal; Alcohol Use, Affecting Fetus

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Mobile incentive-based intervention

Contingent incentives on abstinence from alcohol; Text-based health promotion support

Group Type EXPERIMENTAL

Mobile incentive-based intervention

Intervention Type BEHAVIORAL

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.

Interventions

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Mobile incentive-based intervention

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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* 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
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Medical Research Council, South Africa

OTHER

Sponsor Role collaborator

National Institute on Alcohol Abuse and Alcoholism (NIAAA)

NIH

Sponsor Role collaborator

RTI International

OTHER

Sponsor Role lead

Responsible Party

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Yukiko Washio

Senior Research Psychologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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South African Medical Research Council

Cape Town, , South Africa

Site Status

Countries

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South Africa

References

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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.

Reference Type DERIVED
PMID: 40734177 (View on PubMed)

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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R21AA029048

Identifier Type: NIH

Identifier Source: secondary_id

View Link

0217974

Identifier Type: -

Identifier Source: org_study_id

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