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Native-Changing High-risk Alcohol Use and Increasing Contraception Effectiveness Study (Native-CHOICES)

Primary Purpose

Contraceptive Usage, Alcohol Use Complicating Childbirth, Alcohol Drinking

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Native-CHOICES
Sponsored by
Washington State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Contraceptive Usage

Eligibility Criteria

18 Years - 44 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Native American Woman
  • 18-44 years old at the time of recruitment
  • Self-report high-risk drinking behavior (average 8 or more drinks per week) or episodes of binge drinking (four or more drinks on a single occasion) in the past 90 days
  • Have vaginal sex with a male partner in the past 30 days

Exclusion Criteria:

  • Diagnosed as infertile
  • Pregnant
  • Effectively using contraceptives defined by standard methods
  • Living in a household with someone who is already enrolled in the study

Sites / Locations

  • Missouri Breaks Industries Research IncRecruiting
  • Missouri Breaks Industries Research IncRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Native CHOICES Intervention

Wait-list Control Group

Arm Description

Native-CHOICES will comprise usual care plus 2 MI sessions delivered over 4 weeks; a contraception counseling session at a local clinic; and 3 months of electronic messaging to boost the effects of MI and counseling by increasing perceptions of social connection and social support for behavior change. Contraception counseling will be completed within 2 weeks after the second MI session, so the maximum duration of MI and counseling for each participant will be 6 weeks. Electronic messaging will include positive motivational content consistent with alcohol and contraception use goals set in the MI sessions.

The control condition will comprise usual care for the 6-month study period, with a wait-list design that offers women the Native- CHOICES program after they have completed the 6-month data collection.

Outcomes

Primary Outcome Measures

Reduction in alcohol exposed pregnancy
Our primary outcome is reduction in risk of alcohol exposed pregnancy, defined as no heavy or binge drinking or effective contraception use, or both.

Secondary Outcome Measures

Full Information

First Posted
April 25, 2019
Last Updated
April 26, 2023
Sponsor
Washington State University
Collaborators
University of Colorado, Denver, Sanford Research, Missouri Breaks Industries Research, Inc., University of Minnesota
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1. Study Identification

Unique Protocol Identification Number
NCT03930342
Brief Title
Native-Changing High-risk Alcohol Use and Increasing Contraception Effectiveness Study
Acronym
Native-CHOICES
Official Title
Native-Changing High-risk Alcohol Use and Increasing Contraception Effectiveness Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 28, 2019 (Actual)
Primary Completion Date
October 30, 2023 (Anticipated)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Washington State University
Collaborators
University of Colorado, Denver, Sanford Research, Missouri Breaks Industries Research, Inc., University of Minnesota

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Native CHOICES is a randomized controlled trial of an adapted intervention to reduce the risk of alcohol exposed pregnancies in American Indians and Alaska Natives (AI/ANs). We will enroll 350 AI/AN women living on the Cheyenne River Sioux Indian Reservation or in Rapid City in South Dakota who are 18-44 years old, have risky drinking behaviors, are not currently pregnant but are able to become pregnant, and are sexually active but not using effective contraception.
Detailed Description
Fetal alcohol spectrum disorder (FASD) prevalence is up to 10 times higher in American Indians and Alaska Natives (AI/ANs) than in the general US population, yet FASD is 100% preventable. Even moderate alcohol use during pregnancy can affect fetal growth and behavioral outcomes. Alcohol use disorders and binge drinking in women are among the strongest risk factors for FASD in their offspring. AI/ANs have the highest prevalence of alcohol use disorders among US racial and ethnic groups, and are the most likely to engage in binge drinking during pregnancy. A growing consensus indicates that prevention of alcohol-exposed pregnancy must begin before conception. One promising approach is the Changing High-risk Alcohol Use and Increasing Contraception Effectiveness Study (CHOICES), which combines motivational interviewing with contraception counseling for non-pregnant women. In a randomized trial, women receiving CHOICES were 36% more likely to have reduced risk for alcohol-exposed pregnancies after 6 months than women receiving usual care, but the trial did not enroll AI/ANs or rural women. Although the Centers for Disease Control and Prevention has recommended its dissemination, the public health value and cost-effectiveness of CHOICES in AI/ANs is unknown. We propose a randomized controlled trial of an adapted intervention - Native-CHOICES - to reduce risk of alcohol exposed pregnancies in AI/ANs. We will enroll 350 AI/AN women living on the Cheyenne River Sioux Indian Reservation or in Rapid City in South Dakota who are 18-44 years old, have risky drinking behaviors, are not currently pregnant but are able to become pregnant, and are sexually active but not using effective contraception. Native-CHOICES will consist of 2 motivational interviewing sessions plus 1 contraceptive counseling session over 4 weeks, with supportive electronic messaging for 3 months to increase perceived social connectedness and support for modifying drinking behavior and using contraception.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Contraceptive Usage, Alcohol Use Complicating Childbirth, Alcohol Drinking

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Women will be randomized 1:1 to the intervention or usual care conditions.
Masking
Participant
Allocation
Randomized
Enrollment
350 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Native CHOICES Intervention
Arm Type
Experimental
Arm Description
Native-CHOICES will comprise usual care plus 2 MI sessions delivered over 4 weeks; a contraception counseling session at a local clinic; and 3 months of electronic messaging to boost the effects of MI and counseling by increasing perceptions of social connection and social support for behavior change. Contraception counseling will be completed within 2 weeks after the second MI session, so the maximum duration of MI and counseling for each participant will be 6 weeks. Electronic messaging will include positive motivational content consistent with alcohol and contraception use goals set in the MI sessions.
Arm Title
Wait-list Control Group
Arm Type
No Intervention
Arm Description
The control condition will comprise usual care for the 6-month study period, with a wait-list design that offers women the Native- CHOICES program after they have completed the 6-month data collection.
Intervention Type
Behavioral
Intervention Name(s)
Native-CHOICES
Intervention Description
Native CHOICES is a behavioral intervention for prevention of prenatal alcohol exposure in women at high risk for alcohol-exposed pregnancies. The intervention uses motivational interviewing and cognitive-behavioral strategies, and targets adoption of effective contraception and reduction of alcohol use.
Primary Outcome Measure Information:
Title
Reduction in alcohol exposed pregnancy
Description
Our primary outcome is reduction in risk of alcohol exposed pregnancy, defined as no heavy or binge drinking or effective contraception use, or both.
Time Frame
Baseline, 6 weeks, 3 months and 6 months post intervention

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Native American Woman 18-44 years old at the time of recruitment Self-report high-risk drinking behavior (average 8 or more drinks per week) or episodes of binge drinking (four or more drinks on a single occasion) in the past 90 days Have vaginal sex with a male partner in the past 30 days Exclusion Criteria: Diagnosed as infertile Pregnant Effectively using contraceptives defined by standard methods Living in a household with someone who is already enrolled in the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dedra Buchwald, MD
Phone
206-708-8622
Email
dedra.buchwald@wsu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Odile Madesclaire, MPH
Phone
206-708-8617
Email
odile.madesclaire@wsu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dedra Buchwald, MD
Organizational Affiliation
Washington State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Missouri Breaks Industries Research Inc
City
Eagle Butte
State/Province
South Dakota
ZIP/Postal Code
57625
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marcia O'Leary, BSN
Facility Name
Missouri Breaks Industries Research Inc
City
Rapid City
State/Province
South Dakota
ZIP/Postal Code
57701
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marcia O'Leary, BSN

12. IPD Sharing Statement

Plan to Share IPD
No

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Native-Changing High-risk Alcohol Use and Increasing Contraception Effectiveness Study

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