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Clinical Trials/NCT02337361
NCT02337361
Completed
Not Applicable

Preparing a Computerized Tool for Preventing Prenatal Drinking for a Larger Trial

Public Health Institute, California2 sites in 1 country185 target enrollmentFebruary 22, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Foetal Exposure During Pregnancy
Sponsor
Public Health Institute, California
Enrollment
185
Locations
2
Primary Endpoint
Number of Participants Reporting Weekly Alcohol Use
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

An innovative, self-administered computerized screening and brief intervention (SBI) for drinking during pregnancy will be adapted for use with non-pregnant childbearing age women and its efficacy will be tested in a small trial. Study findings will inform a larger randomized control trial for a primary prevention tool with the potential for broad health impact.

Detailed Description

This study evaluates a recently piloted, self-administered, computerized tool for reducing prenatal drinking that added novel components of drink size assessment and drink size feedback to traditional screening and brief intervention (SBI). The bilingual (English and Spanish) electronic SBI or "e-SBI" will be adapted for use with non-pregnant women and a small trial of its efficacy will be conducted in two public health clinics. The effects of drink size assessment by itself and of depression as a modifier of e-SBI efficacy will also be studied. Study findings will help design a larger trial of e-SBI's efficacy for reducing prenatal alcohol use. An experimental design will be used for the proposed small trial. Two hundred women, who have not been pregnant in the past year and report alcohol at risky levels will be randomly assigned to e-SBI or usual care. Participants will complete baseline, 3-month and 6-month follow-up assessments. These assessments will examine drinking and pregnancy as well as possible negative outcomes, such as increased drug use associated with the e-SBI. To address methodological limitations in prior research, the study design incorporates drink size assessment to better measure drinking outcomes, minimizes assessment reactivity for controls at baseline, and includes a booster e-SBI at the 3-month follow up. This allows for the examination of whether drink size assessment reduces drinking by itself and if its effects are equivalent to that of the full e-SBI. With these design innovations, the study is expected to provide information that can be more rigorously assessed in a subsequent multi-arm trial. Because it sets the stage for a Phase II trial of e-SBI efficacy for reducing prenatal alcohol use, our proposed study is of significance for improved maternal and child health. Findings will also impact the larger intervention literature on cost-effective strategies to reduce alcohol-related harm.

Registry
clinicaltrials.gov
Start Date
February 22, 2016
End Date
August 31, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Public Health Institute, California
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • not pregnant in the last 6 months, drank alcohol in the past year, alcohol consumption was at risky levels,

Exclusion Criteria

  • not fluent in english or spanish,

Outcomes

Primary Outcomes

Number of Participants Reporting Weekly Alcohol Use

Time Frame: baseline, 3 month, 6 month

weekly alcohol use is defined as at least drinking once a week or more often

Number of Participants Reporting Risky Alcohol Use

Time Frame: baseline, 3 months, 6 months

Risky alcohol use is defined as drinking 8 or more drinks in a week or 3 or more drinks in a day. Risky alcohol use is measured by frequency of any alcohol use, number of usual and maximum drinks in a drinking day, and frequency of drinking 3 or more drinks containing alcohol

Number of Participants Reporting Heavy Alcohol Use

Time Frame: baseline, 3 month, 6 month

heavy alcohol use is defined as self-reported maximum number of drinks in a day of 5 or more drinks

Secondary Outcomes

  • Number of Participants Reporting Any Tobacco Use(baseline , 3 months, 6 months)
  • Number of Participants Reporting Any Drug Use(baseline, 3 month, 6 month)
  • Number of Participants Reporting Frequent Sugar Sweetened Beverage Use(baseline, 3 months, 6 months)
  • Number of Participants Reporting Significant Depression(baseline, 3 months, 6 months)

Study Sites (2)

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