Skip to main content
Clinical Trials/NCT04376346
NCT04376346CompletedNot Applicable

Preventing Alcohol Exposed Pregnancy Among Urban Native Young Women: Mobile CHOICES

University of Colorado, Denver1 site in 1 country439 target enrollmentStarted: August 4, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
439
Locations
1
Primary Endpoint
Alcohol Use

Study Overview

Brief Summary

Fetal Alcohol Syndrome Disorders (FASD) result in lifelong disability and are a leading cause of preventable birth defects in the US. Urban American Indian and Alaska Native (AIAN) young women are at high risk for alcohol exposed pregnancies (AEPs) which can cause FASD. In this project, the inverstigators will test the effectiveness of a culturally adapted mobile health intervention to prevent AEP, using social media to recruit AIAN young women from urban centers across the nation.

Detailed Description

The proposed project builds on a prior NIAAA-funded project which used intensive community-based participatory research (CBPR) methods to adapt CHOICES, an evidence-based brief alcohol-exposed pregnancy (AEP) prevention intervention supported by the CDC, to American Indian Youth CHOICES (AIY-C). AIY-C contains features that make it highly amenable to mHealth approaches, including a framework for integrating diverse cultural teachings, few modules of short duration, and concrete opportunities for goal-setting and achievement. Innovative for this population is the plan to recruit young AIAN women from major urban areas in the US through social media-and to deliver AIY-C via mobile devices, increasingly ubiquitous among AIAN young adults. While social media recruitment and mHealth interventions are not new, only very recently have they been used with AIAN populations. The investigators will partner with urban AIAN organizations to guide us through social media recruitment strategies, mHealth intervention translation and implementation, and evaluation in urban AIAN settings. The investigators propose 3 specific aims: (1) Develop and pilot social-media-based recruitment strategies for urban AIAN young women; (2) translate AIY-C for mHealth delivery through an iterative and theoretically driven process and pilot the developed translated mHealth AIY-C intervention; and (3) recruit 700 (final N=525) urban AIAN young women using identified social media strategies, and conduct an RCT to rigorously evaluate the effectiveness of the mHealth translation of AIY-C for preventing AEP and FASD.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
16 Years to 20 Years (Child, Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Identifies as American Indian or Alaska Native (AIAN)
  • •Biologically female
  • •16-20 years old
  • •Not pregnant
  • •Not living in tribal reservation or in an Alaska Native Village
  • •Live in an urban area that is at least 50,000 in population
  • •Not breastfeeding
  • •Has an email account
  • •Has a smart phone

Exclusion Criteria

  • •Age 15 or younger, and 21 or older
  • •Biologically male
  • •Pregnant or breastfeeding women
  • •People who live on a tribal land or in communities with less than 50,000 in population
  • •Reside in the state of Alaska (until study obtains local IRB approval)

Arms & Interventions

Intervention Arm

Experimental

Participants in the intervention arm will complete the AIY-C curriculum that has been translated for mHealth delivery. This includes completing various activities such as completing their own risk assessment when it comes to AEP and setting goals for themselves.

Intervention: Native WYSE CHOICES (Behavioral)

Control Arm

No Intervention

Participants in the control arm will complete activities that are carefully designed under different topics than the intervention arm. In this regard, participants will complete various activities such as quizzes, interactive games and videos. The investigators will ensure that participants in both arms will spend similar time on completing the activities.

Outcomes

Primary Outcomes

Alcohol Use

Time Frame: 12 months

Had at least one alcoholic drink in past 30 days (Y/N)

Effective Contraceptive Use

Time Frame: 12 months

Effective contraceptive use (including abstinence), measured by past 30-day vaginal sexual abstinence or, if sexually active, 30 day use of effective contraception at intercourse.

Alcohol Use

Time Frame: 12 months

Had at least one alcoholic drink in past 30 days (Y/N)

Effective Contraceptive Use

Time Frame: 12 months

Effective contraceptive use (including abstinence), measured by past 30-day vaginal sexual abstinence or, if sexually active, 30 day use of effective contraception at intercourse.

Alcohol Use

Time Frame: Baseline

Had at least one alcoholic drink in past 30 days (Y/N)

Alcohol Use

Time Frame: 1 month

Had at least one alcoholic drink in past 30 days (Y/N)

Alcohol Use

Time Frame: 6 months

Had at least one alcoholic drink in past 30 days (Y/N)

Effective Contraceptive Use

Time Frame: Baseline

Effective contraceptive use (including abstinence), measured by past 30-day vaginal sexual abstinence or, if sexually active, 30 day use of effective contraception at intercourse.

Effective Contraceptive Use

Time Frame: 1 months

Effective contraceptive use (including abstinence), measured by past 30-day vaginal sexual abstinence or, if sexually active, 30 day use of effective contraception at intercourse.

Effective Contraceptive Use

Time Frame: 6 months

Effective contraceptive use (including abstinence), measured by past 30-day vaginal sexual abstinence or, if sexually active, 30 day use of effective contraception at intercourse.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials