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Brief alcohol intervention to reduce risky drinking in pregnancy: a pilot randomised controlled trial

Brief alcohol intervention to reduce risky drinking in pregnancy: a pilot randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN43218782
Enrollment
120
Registered
2011-08-17
Start date
2012-01-02
Completion date
Unknown
Last updated
2018-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topic: Primary Care Research Network for England

Interventions

Brief alcohol advice, Control condition - 5 minutes of simple structured alcohol advice delivered by midwife [Treatment As Usual (TAU)]. Brief alcohol intervention, Experimental condition - 5 minutes

Sponsors

Newcastle upon Tyne Hospitals NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Women attending routine antenatal care 2. Women who book an antenatal appointment before 16 weeks gestation 3. Women who are aged 18 years or above 4. Women who provide verbal agreement to be screened for alcohol (written consent is not gathered for screening as this is usual practice in antenatal care) 5. Women who screen positive for risky alcohol use [score of 5+ on the Alcohol Use Disorders Identification Test(AUDIT-C)] 6. Women who give written consent to participate in the research; Target Gender: Female ; Lower Age Limit 18 years

Exclusion criteria

Exclusion criteria: 1. Women with pregnancy complications (e.g. diabetes, congenital anomaly) 2. Women with multiple pregnancies 3. Women who book an antenatal appointment after 16 weeks gestation 4. Women with a history of substance use and/or alcohol dependence 5. Women who do not speak English sufficiently to participate 6. Women who are experiencing a severe mental or physical illness which is likely to impact upon the intervention or ability to be followed-up 7. Women who are already participating in other alcohol-related research 8. Women who lack the cognitive capacity to understand the research and what is involved (and are therefore unable to provide informed consent to participate)

Design outcomes

Primary

MeasureTime frame
Participants recruited & retained; Timepoint(s): Baseline, 3rd trimester of pregnancy (6 months), 6 months post partum

Secondary

MeasureTime frame
Alcohol consumption; Timepoint(s): In third trimester (6 months from baseline)

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 25, 2026