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

Sponsor
University of Colorado, Denver (Other)
Overall Status
Recruiting
CT.gov ID
NCT04376346
Collaborator
National Institute on Alcohol Abuse and Alcoholism (NIAAA) (NIH)
700
1
2
23.9
29.3

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Native WYSE CHOICES
N/A

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
Anticipated Enrollment :
700 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Preventing Alcohol Exposed Pregnancy Among Urban Native Young Women: Mobile CHOICES
Actual Study Start Date :
Aug 4, 2021
Anticipated Primary Completion Date :
Jul 31, 2022
Anticipated Study Completion Date :
Jul 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Arm

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.

Behavioral: Native WYSE CHOICES
Native WYSE (Women, Young, Strong, and Empowered) CHOICES (Changing High-risk alcohOl use and Increasing Contraception Effectiveness Study) is an alcohol-exposed pregnancy prevention program that translates CHOICES, an evidence-based targeted intervention, into an mHealth universal intervention for young urban American Indian/Alaska Native (AI/AN) women ages 16-20.

No Intervention: Control Arm

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.

Outcome Measures

Primary Outcome Measures

  1. Alcohol Use [Baseline]

    Number of days in past 30 had at least one alcoholic drink.

  2. Alcohol Use [2 months]

    Number of days in past 30 had at least one alcoholic drink.

  3. Alcohol Use [6 months]

    Number of days in past 30 had at least one alcoholic drink.

  4. Alcohol Use [12 months]

    Number of days in past 30 had at least one alcoholic drink.

  5. Effective Contraceptive Use [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.

  6. Effective Contraceptive Use [2 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.

  7. Effective Contraceptive Use [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.

  8. Effective Contraceptive Use [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years to 20 Years
Sexes Eligible for Study:
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

  • Not AIAN

  • 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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Colorado- Anschutz Medical Campus Aurora Colorado United States 80045

Sponsors and Collaborators

  • University of Colorado, Denver
  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Investigators

  • Principal Investigator: Carol Kaufman, PhD, University of Colorado - Anschutz Medical Campus
  • Principal Investigator: Michelle Sarche, PhD, University of Colorado - Anschutz Medical Campus

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Colorado, Denver
ClinicalTrials.gov Identifier:
NCT04376346
Other Study ID Numbers:
  • 18-0574
  • R01AA025603
First Posted:
May 6, 2020
Last Update Posted:
Aug 19, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 19, 2021