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Alcohol Use DisorderCAP-PreNCT06853873

Counseling for Alcohol Problems in Pregnancy (CAP-Pre) Phase II

A study testing The Counselling for Alcohol Problems in Pregnancy (CAP-Pre) intervention in people with Alcohol Use Disorder, run by Leibniz Institute for Prevention Research and Epidemiology - BIPS GmbH at 1 site in South Africa.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Purpose: This study is testing a new counseling program called Counselling for Alcohol Problems in Pregnancy or CAP-Pre, designed to help pregnant women in South Africa to reduce their alcohol use and improve their well-being. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Alcohol Use Disorder
What is being tested?
The Counselling for Alcohol Problems in Pregnancy (CAP-Pre) intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 siteSouth Africa
Study dates
10 Feb 2025to Jul 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • • Pregnant women ≤28 weeks gestation.
  • Alcohol Use Risk: Hazardous alcohol use, defined as an Alcohol Use Disorder Identification Test (AUDIT) score of 8-20.
  • Age ≥18 years old at the time of recruitment.
  • Consent: Ability to provide written informed consent and willingness to participate in the study

Who cannot join

  • Severe Mental Health Conditions: Diagnosed psychotic disorders or severe cognitive impairment that may interfere with participation.
  • High-Risk Pregnancy: Presence of significant pregnancy complications that require specialized medical care.
  • Substance Dependence (Other Than Alcohol): Current dependence on drugs other than alcohol and tobacco requiring specialized treatment.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

South Africa1 site
  • South African Medical Research Council (SAMRC)

    Cape Town, PO Box 19070, Tygerberg, 7505

Other trials in South Africa

About this study

Purpose: This study is testing a new counseling program called Counselling for Alcohol Problems in Pregnancy or CAP-Pre, designed to help pregnant women in South Africa to reduce their alcohol use and improve their well-being. Alcohol use during pregnancy can harm babies, leading to Fetal Alcohol Spectrum Disorders (FASD), which can cause lifelong health and developmental problems. Currently, there are no community-based support programs to help pregnant women struggling with alcohol use.

What Happens in the Study? 40 pregnant women will take part in the study and will be randomly assigned to one of two groups:

Read more
  1. CAP-Pre + Standard Health Advice - Women will receive five counseling sessions to help them reduce drinking, plus usual pregnancy care.
  2. Standard Health Advice Only - Women will receive usual pregnancy care and an information booklet on alcohol use in pregnancy.

The study will test:

The study will evaluate if CAP-Pre is easy to deliver, acceptable, and helps women to drink less. (measured by self-report and a blood test).

Why Is This Important? South Africa has the highest rates of FASD in the world, but most pregnant women do not receive specialized support for harmful alcohol use. If this pilot study is successful, it will help prepare for a more extensive study to test whether CAP-Pre can be widely used in antenatal care programs.

Who Is Involved? The study is run by researchers from Germany and South Africa, with funding from the German Alliance for Global Health Research.

Read the detailed description

South Africa has the highest prevalence of Fetal Alcohol Spectrum Disorders (FASD) globally, with alcohol use during pregnancy being prevalent in low-resource settings. However, there is no structured, community-based psychological support available for pregnant women who consume alcohol at harmful levels. The Counselling for Alcohol Problems in Pregnancy (CAP-Pre) intervention is a brief psychological counseling program designed to:

  • Support pregnant women in reducing alcohol use through motivational interviewing (MI) and cognitive-behavioral techniques (CBT).
  • Improve maternal well-being by addressing underlying stressors and barriers to change.
  • Be delivered by community health workers (CHWs) in a scalable, task-shifted approach.

This pilot randomized controlled trial (RCT) aims to evaluate the CAP-Pre intervention's perceived effectiveness, feasibility, and acceptability in preparation for a definitive RCT.

Study Design Type: Parallel-arm, single-blind, individually randomized controlled trial (RCT).

Setting: Community-based antenatal care program, Cape Flats, Western Cape, South Africa.

Participants: 40 pregnant women screened for the following eligibility criteria

Inclusion:

  • ≥18 years old, ≤28 weeks pregnant.
  • AUDIT score 8-20 (indicating hazardous alcohol use).

Exclusion:

  • Severe psychiatric disorders.
  • High-risk pregnancy complications. Recruitment Sites: Community outreach and antenatal clinics.

Randomization: 1:1 allocation to:

  • CAP-Pre + Enhanced Usual Care (EUC) (Intervention)
  • Enhanced Usual Care (EUC) only (Control) Intervention and Control Groups Intervention: CAP-Pre + Enhanced Usual Care (EUC) (n=20) Five structured 60-minute counseling sessions (weekly, CHW-delivered).

Key components:

Motivational interviewing (MI) to enhance behavior change. Cognitive-behavioral strategies (CBT) for managing alcohol cravings. Goal-setting and self-monitoring for tracking progress. Problem-solving techniques and social support enhancement. Control: Enhanced Usual Care (EUC) (n=20) Information booklet on alcohol use in pregnancy. Referral to antenatal services if needed. No structured counseling was provided.

Data Collection and Outcome Measures

Data Collection Timeline:

Baseline assessment before randomization and Post-intervention assessment on alcohol use, mental health, and qualitative feedback Primary Outcomes

Reduction in alcohol consumption measured through:

Self-Reported Alcohol Use: Alcohol consumption will be assessed using the Alcohol Timeline Follow Back (TLFB) method to estimate daily drinking volume over the past months.

Secondary Outcomes

  1. Biological Markers for alcohol consumption: Phosphatidyl ethanol (PeTH) through Dried Blood Spot (DBS) Collection. PeTH is a direct biomarker of alcohol consumption that is formed only in the presence of ethanol. It is highly specific and sensitive in detecting alcohol use over the past 2-3 weeks.
  2. Psychosocial Functioning: Assessed using the WHO-Disability Assessment Schedule (WHO-DAS). WHO-DAS 2.0 is a standardized instrument developed by the World Health Organization (WHO) to assess functional impairment and disability across multiple life domains. It evaluates the impact of mental and physical health conditions on daily activities and social participation.
  3. Depressive Symptoms: Evaluated using the Edinburgh Postnatal Depression Scale (EPDS). EPDS is a 10-item self-report measure designed to screen for perinatal depression in pregnant and postpartum women.
  4. Alcohol-Related Consequences: Measured with the Alcohol Use Disorder Identification Test - Consumption (AUDIT-C). AUDIT-C is a brief, 3-item screening tool derived from the full 10-item Alcohol Use Disorders Identification Test (AUDIT) to identify individuals at risk for hazardous drinking and alcohol use disorders (AUDs).
  5. Family and Social Support: Assessed using a 10-item structured questionnaire measuring the availability and perceived adequacy of social support across various domains, such as emotional, instrumental, and informational support.
  6. Perceived Usefulness of Counselling: Evaluated through qualitative pre and post-intervention interviews, exploring participant expectations, experiences, perceptions of counseling, and perceived benefits or challenges.

Baseline Covariates:

Additional Covariates Collected at Baseline

  1. Demographic and Socioeconomic Information: Age, education, and socioeconomic status.
  2. Substance Use and Risk Factors: Self-reported past-month use of tobacco and other substances.
  3. Partner Substance Use: Self-reported data on household and partner alcohol/drug use.
  4. Intimate Partner Violence (IPV) \& History of Trauma: Self-reported experiences of violence, abuse, and health-related risks.
  5. Childhood Adversity and Life Stressors: Self-reported early trauma and current stressors.

Analysis Plan We will analyze and report data following CONSORT guidelines for pilot and feasibility trials. Analyses for the pilot RCT will mainly be descriptive to describe recruitment and response rates, process data, and retention at 3 months.

Ethical Considerations This study poses minimal risks, including minor discomfort from blood sampling and potential mental distress during sessions. Confidentiality will be protected through strict data security, staff confidentiality agreements, and ethical training. PeTH blood collection will follow infection control protocols and be conducted by trained staff. Mental distress risks will be minimized through participant choice, referrals for support, and staff supervision. The study has ethical approval from the South African MRC, and participation is voluntary, with the right to withdraw at any time.

Output A contextually adapted program of care (called CAP-PRE) for pregnant women who misuse alcohol that can be tested for effectiveness and cost-effectiveness in a larger, definitive RCT.

Being tested
The Counselling for Alcohol Problems in Pregnancy (CAP-Pre) intervention
Keywords
Alcohol misuse, pregnancy, Women, Psychoeducation, Lay Health Workers, South Africa, Alcohol use in Pregnancy, Counseling Sessions, Psychoeducational Intervention
Medical subject headings
Alcoholism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • The Counselling for Alcohol Problems in Pregnancy (CAP-Pre) interventionBehavioural

    Also called CAP-PRE

    Five structured 60-minute counseling sessions (weekly, CHW-delivered).

    Key components:

    Motivational interviewing (MI) to enhance behavior change. Cognitive-behavioral strategies (CBT) for managing alcohol cravings. Goal-setting and self-monitoring for tracking progress. Problem-solving techniques and social support enhancement.

Study groups in NCT06853873
Study groupRoleWhat they receive
Enhanced Usual Care (EUC)No interventionInformation booklet on alcohol use in pregnancy. Referral to antenatal services if needed. No structured counseling was provided.
CAP-Pre + Enhanced Usual CareExperimentalThe Counselling for Alcohol Problems in Pregnancy (CAP-Pre) intervention
Receives: Behavioral: The Counselling for Alcohol Problems in Pregnancy (CAP-Pre) intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Self-Reported Alcohol Consumption assessed using the Alcohol Timeline Follow Back (TLFB)

    Alcohol use will be assessed using the Alcohol Timeline Follow Back (TLFB) method, a retrospective self-report tool that estimates daily drinking volume over the past month. This method provides a structured recall of alcohol consumption patterns, allowing for detailed quantification of drinking behavior.

    Measured: Changes from Baseline to Post Intervention in 6 weeks

Secondary outcomes (4)
  1. Biological Marker of Alcohol Use assessed using Phosphatidylethanol (PeTH) testing

    Phosphatidylethanol (PeTH) testing, a highly specific and sensitive biomarker for alcohol consumption, will be conducted via finger-prick blood samples. PeTH levels differentiate heavy vs. occasional drinking over the past 2-3 weeks and detect recent abstinence. Dried Blood Spots (DBS) will be exported for analysis at the United States Drug Testing Laboratories (USDTL) under an established material transfer agreement, ensuring high-standard laboratory processing.

    Measured: Changes from Baseline to Post Intervention in 6 weeks

  2. Psychosocial functioning assessed using WHO-Disability Assessment Schedule (WHO-DAS)

    Measured using the WHO-Disability Assessment Schedule (WHO-DAS) evaluates functional impairment across multiple life domains, including cognition, mobility, self-care, and social participation.

    Measured: Changes from Baseline to Post Intervention in 6 weeks

  3. Depressive Symptoms assessed using Edinburgh Postnatal Depression Scale (EPDS)

    Assessed using the Edinburgh Postnatal Depression Scale (EPDS), a validated screening tool for detecting perinatal depression in pregnant women. Higher scores indicate greater symptom severity, informing potential mental health support needs.

    Measured: Changes from Baseline to Post Intervention in 6 weeks

  4. Alcohol-Related Consequences assessed using Alcohol Use Disorder Identification Test - Consumption (AUDIT-C)

    Measured using the Alcohol Use Disorder Identification Test - Consumption (AUDIT-C), a validated screening tool for identifying hazardous drinking patterns and assessing alcohol-related harm during pregnancy.

    Measured: Changes from Baseline to Post Intervention in 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Mar 2025
  2. Study start10 Feb 2025
  3. Primary completionMay 2025 (estimated)
  4. Study completionJul 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
The study follows a parallel-arm, individually randomized controlled trial (RCT) design to assess the feasibility, acceptability, and preliminary effectiveness of the Counselling for Alcohol Problems in Pregnancy (CAP-Pre) intervention. Participants (n=40 pregnant women, ≤28 weeks gestation) will be randomly assigned (1:1) to either: Intervention Group: CAP-Pre plus Enhanced Usual Care (EUC), consisting of five manualized counselling sessions delivered by trained community health workers (CHWs). Control Group: EUC only, including an information booklet on alcohol use in pregnancy but no structured counselling. Primary outcomes focus on alcohol consumption, measured via self-report (TLFB). Secondary outcomes assess biomarkers for alcohol consumption PeTH testing, psychosocial functioning (WHO-DAS), depressive symptoms (EPDS), alcohol-related consequences (AUDIT-C) and perceived usefulness (qualitative interviews). Data will be collected at baseline and intervention
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06853873
Sponsor's protocol ID
01KA2401A
Acronym
CAP-Pre
Status last verified
Feb 2025
First submitted
25 Feb 2025
Last updated
3 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: The data is subject to strict confidentiality agreements as per the ethical approval obtained, and sharing it publicly could compromise participant privacy.

Publications

  • Wan X, Fang M, Chen T, Wang H, Zhou Q, Wei Y, Zheng L, Zhou Y, Chen K. Corrigendum to "The mechanism of low-dose radiation-induced upregulation of immune checkpoint molecule expression in lung cancer cells" [Biochem. Biophys. Res. Commun. 608 (2022 Jun 11) 102-107, doi: 10.1016/j.bbrc.2022.03.158. Epub 2022 Apr 2.PMID: 35397421]. Biochem Biophys Res Commun. 2023 Oct 26:149132. doi: 10.1016/j.bbrc.2023.149132. Online ahead of print. No abstract available.

    PubMed 39492324
  • Petersen Williams P, Erasmus J, Myers B, Nadkarni A, Fuhr DC. Community-based counselling programme for pregnant women with alcohol problems in Cape Town, South Africa: a qualitative study of the views of pregnant women and healthcare professionals. Front Psychiatry. 2023 Jul 6;14:1203835. doi: 10.3389/fpsyt.2023.1203835. eCollection 2023.

    PubMed 37484680
  • Petersen Williams P, Lange IL, Erasmus J, Erasmus-Claassen LA, Saleem M, Reigl LS, Wolf M, Schaub S, Buck C, Nadkarni A, Fuhr DC. A feasibility trial of a psychological intervention for addressing alcohol problems during pregnancy: a study protocol. Pilot Feasibility Stud. 2026 Oct 9;12(1):145. doi: 10.1186/s40814-026-01932-5.

    PubMed 42855736

Questions about this trial

What is this clinical trial studying?

A study testing The Counselling for Alcohol Problems in Pregnancy (CAP-Pre) intervention in people with Alcohol Use Disorder, run by Leibniz Institute for Prevention Research and Epidemiology - BIPS GmbH at 1 site in South Africa.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 3 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in South Africa. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Self-Reported Alcohol Consumption assessed using the Alcohol Timeline Follow Back (TLFB) (time frame: Changes from Baseline to Post Intervention in 6 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06853873, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Mar 2025.

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