Development of Education Materials for Prevention of FAS in Russia

Development of Education Materials for Prevention of Fetal Alcohol Syndrome (FAS) in Russia

This study is designed to increase knowledge and awareness to prevent Fetal Alcohol Syndrome in Russian children through development of printed FAS education materials targeting women of childbearing age in Russia. Alcohol abuse is a major public health problem in Russia. The rates of FAS and Alcohol Related Neurodevelopmental Disorders (ARND) in Russia are not precisely known. At this time, there are no programs to prevent FAS in Russia. The results of our previous study, focus groups with health professionals, pregnant women and their partners, non-pregnant women, and women with alcohol dependency, indicated limited knowledge about FAS, misconceptions about alcohol use during pregnancy, and a lack of materials and print resources related to this topic. Based on the initial findings, this proposal aims to develop and evaluate in a clinical trial informational brochures for women to increase knowledge and reduce drinking during pregnancy in Russia. The main hypotheses to be tested are:

• 1. Compared to the control group (CG) of women who receive a standard locally available flyer with health recommendations, women in the experimental groups who are exposed to printed information on FAS will show significantly more knowledge about FAS, significantly less acceptance of any alcohol use during pregnancy, and reduced drinking at one month follow-up assessment.
• 2. The group exposed to a brochure with negative images (IGN - Intervention group with a "negative brochure") regarding drinking during pregnancy will show significantly greater change in the predicted directions compared to the group exposed to positive images (IGP - Intervention group with a "positive" brochure) at the one month follow-up assessment.

Study Overview

• Status: Completed
• Conditions: Fetal Alcohol Spectrum Disorders; Fetal Alcohol Syndrome (FAS); Alcohol Related Neurodevelopmental Disorder; Alcohol Use Complicating Pregnancy, Unspecified Trimester
• Intervention / Treatment: Behavioral: Positive FASD education brochure; Behavioral: Negative FASD education brochure; Behavioral: Active comparator (a general women's health brochure)

Detailed Description

The study utilizes a randomized controlled trial design to test the two types of brochures (with positive vs. negative images and statements) to determine if either approach has more effect on women's alcohol consumption.

Pregnant and non-pregnant childbearing age women will be recruited at women's clinics and randomly assigned to participate in one of three groups: (1) participants will review the brochures that present information on FAS and alcohol use in pregnancy with positive images, (2) participants will review the brochures that that present information on FAS and alcohol use in pregnancy with negative, vivid images, and (3) participants will receive a general health information material that is available at their local clinics.

All study participants will complete a baseline survey assessing their attitudes toward drinking during pregnancy, knowledge of FAS, and current alcohol use. After that, the intervention will be conducted. The women in the two experimental groups will receive a brochure with either positive (IGP) or negative (IGN) images. The women will be asked to read one of two brochures in the presence of the data collector. If the participants ask questions, the data collector will redirect the participants to material in the brochure. Following the intervention, the women in the experimental groups will complete a brief questionnaire to assess their emotional responses to the materials and perceived effects. The women assigned to the control group (CG) will be asked to read a brochure on general aspects of women's' health. At a one-month follow-up, women in all three groups will complete a post-test of self-reported alcohol consumption, knowledge about prenatal effects of alcohol and FAS, and attitudes to drinking during pregnancy.

• Study Type: Interventional
• Enrollment (Actual): 422
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Russian Federation
  • Nizhny Novgorod, Russian Federation
    • Nizhny Novgorod State Pedagogical University
  • St. Peterburg, Russian Federation
    • St. Petersburg State University
• United States
  • Oklahoma
    • Oklahoma City, Oklahoma, United States, 73104
      • University of Oklahoma

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 44 years (ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

• Women
• Childbearing age (between 18 and 44 years of age)
• Sexually active (any intercourse with a partner in the last year)
• Consume alcohol (any level of alcohol consumption in the last year)

Exclusion Criteria:

• None

Study Plan

How is the study designed?

Design Details

• Primary Purpose: PREVENTION
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: DOUBLE

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Positive Brochure; Women receive a "positive" FASD education brochure with positive images and are asked to read this brochure in the presence of a data collector.	Behavioral: Positive FASD education brochure; Exposure to a positive FASD education brochure
EXPERIMENTAL: Negative Brochure; Women receive a "negative" FASD education brochure with negative, vivid images and are asked to read this brochure in the presence of a data collector.	Behavioral: Negative FASD education brochure; Exposure to a negative FASD education brochure
ACTIVE_COMPARATOR: A general women's health brochure; Women receive a brochure on general aspects of women's health and pregnancy that is available in the Russian language and are asked to read this brochure in the presence of a data collector.	Behavioral: Active comparator (a general women's health brochure); Exposure to a general women's health brochure

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Changes in knowledge about Fetal Alcohol Syndrome (FAS) from baseline	A survey measure assessed knowledge about FAS	1 month follow-up
Changes in attitudes from baseline	A survey measure assessed attitudes and health beliefs related to alcohol use during pregnancy	1 month follow-up
Changes in alcohol consumption from baseline	Interviews assessed self-reported quantity/frequency of alcohol consumption and frequency of binge drinking and a detailed alcohol consumption report was received utilizing the Time Line Follow Back (TLFB) measure.	1 month follow-up

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Responses to brochures	A brief questionnaire to assess women's feedback, perceived effect, and emotional responses to health or FAS education brochures.	After the intervention (reading an information brochure)

Collaborators and Investigators

• Sponsor: University of Oklahoma
• Collaborators: Centers for Disease Control and Prevention
• Investigators: Principal Investigator: Barbara Bonner, PhD, University of Oklahoma

Publications and helpful links

Helpful Links

• Information about the research project, the University of Oklahoma Health Sciences Center (OUHSC) website

Study record dates

Study Major Dates

• Study Start: April 1, 2007
• Primary Completion (ACTUAL): December 1, 2007
• Study Completion (ACTUAL): December 1, 2007

Study Registration Dates

• First Submitted: October 23, 2013
• First Submitted That Met QC Criteria: October 23, 2013
• First Posted (ESTIMATE): October 29, 2013

Study Record Updates

• Last Update Posted (ESTIMATE): October 29, 2013
• Last Update Submitted That Met QC Criteria: October 23, 2013
• Last Verified: October 1, 2013

More Information

Terms related to this study

• Keywords: Prevention; Knowledge; Attitudes; Fetal Alcohol Spectrum Disorders (FASD); Alcohol-Exposed Pregnancy
• Additional Relevant MeSH Terms: Mental Disorders; Chemically-Induced Disorders; Pathologic Processes; Alcohol-Related Disorders; Substance-Related Disorders; Fetal Diseases; Alcohol-Induced Disorders; Syndrome; Disease; Pregnancy Complications; Neurodevelopmental Disorders; Fetal Alcohol Spectrum Disorders
• Other Study ID Numbers: RTO1 2005-999-01