Using Facebook to Support Opioid Recovery Among American Indian Women

Description

The purpose of this study is to find out whether a Facebook group will help Native women in recovery from opioid use.

Conditions

Opioid Use Disorder

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Study Overview

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Study Details

Study overview

The purpose of this study is to find out whether a Facebook group will help Native women in recovery from opioid use.

Facebook Intervention for Preventing Opioid Relapse Among American Indian Women: Wiidookaage'Win Pilot Preparatory Study (Aim 2)

Using Facebook to Support Opioid Recovery Among American Indian Women

Condition
Opioid Use Disorder
Intervention / Treatment

-

Contacts and Locations

Rochester

Mayo Clinic, Rochester, Minnesota, United States, 55901

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. AIAN person based on self-reported race/ethnicity
  • 2. Gender identity as a woman
  • 3. At least 18 years of age with no upper age limit
  • 4. Resides in Minnesota
  • 5. Meets criteria for OUD based on the DSM-5 Checklist (American Psychiatric Association, 2013)
  • 6. Self-reports at least one month of abstinence from opioid use based on TLFB interview and negative urine opiate screen
  • 7. Current use of MOUD
  • 8. Is comfortable speaking and reading English
  • 9. Has an existing Facebook account or willing to set one up
  • 10. Is willing and able to participate in the Facebook intervention for 3 months
  • 11. Has access to broadband internet on a mobile phone/computer/tablet at any location
  • 12. Is willing and able to travel to a community clinic in Minneapolis, Minnesota for the UDS or is willing to and able to complete a virtual Zoom UDS visit.
  • 13. Provides written informed consent
  • 1. Self-reports current suicidality based on the Concise Heath Risk Tracking scale
  • 2. Participated in prior study phases (Aim 1 formative work) of NIDA CTN-0123

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Mayo Clinic,

Christi A Patten, PhD, PRINCIPAL_INVESTIGATOR, Mayo Clinic

Study Record Dates

2024-12