Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT05766761

Reducing Alcohol Exposed Pregnancies

Led by New York University · Updated on 2026-04-13

600

Participants Needed

1

Research Sites

158 weeks

Total Duration

On this page

Sponsors

N

New York University

Lead Sponsor

T

The University of Texas Health Science Center, Houston

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare an active intervention versus a standard of care control in reducing alcohol use among pregnant women. The main questions it aims to answer are whether a motivational intervention can: 1. increase the proportion of women detected with a laboratory-confirmed negative phosphatidylethanol (PEth) test during pregnancy, and 2. reduce the proportion of adverse birth outcomes among infants. Participants will be offered (1) a self-paced computer-delivered alcohol reduction intervention to enhance knowledge, norms, and motivation for alcohol reduction and (2) a nurse-delivered component to reinforce the computer-delivered content and address women's questions. Both components are theory-driven, based on Motivational Enhancement Theory (MET), and use motivational strategies to promote alcohol reduction.

CONDITIONS

Official Title

Reducing Alcohol Exposed Pregnancies

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years and above
  • Pregnant with gestational age of 28 weeks or less
  • Recent alcohol use reported within the previous 30 days
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Not pregnant or gestational age over 28 weeks
  • No recent alcohol use reported

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The University of Texas Health Science Center, Houston

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

R

Rebecca Lunstroth

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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