Using Facebook to Support Opioid Recovery Among American Indian Women
NCT ID: NCT05995886
Last Updated: 2026-01-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
60 participants
INTERVENTIONAL
2023-10-16
2026-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Wiidookaage'win Facebook Group
The Wiidookaage'win Facebook Group is an online, asynchronous group intervention that will run for 3-months with approximately 30 days of content developed. It is private and hidden, meaning only those in the study will be able to see or find the group. It will be moderated by two women from the study team (one AIAN and one biracial). A back-up moderator will also have access to the group. Participants will be able to comment, react, view, and post in the intervention group, and are encouraged to interact with one another.
Wiidookaage'win Facebook Group
An online social media group program that incorporates social support, mindfulness-based, and cultural practices that may support OUD recovery.
Online Resources Landing Page
The Online Resources Landing Page was developed by the study team using https://carrd.co. It includes links to local programs in family services, substance use recovery, legal advocacy, etc. which already exist and may help support their recovery.
No interventions assigned to this group
Interventions
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Wiidookaage'win Facebook Group
An online social media group program that incorporates social support, mindfulness-based, and cultural practices that may support OUD recovery.
Eligibility Criteria
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Inclusion Criteria
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
Exclusion Criteria
2. Participated in prior study phases (Aim 1 formative work) of NIDA CTN-0123
18 Years
FEMALE
No
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
Mayo Clinic
OTHER
Responsible Party
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Christi Patten
Professor of Psychology
Principal Investigators
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Christi A Patten, PhD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic
Rochester, Minnesota, United States
Countries
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Central Contacts
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Facility Contacts
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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DA40316-08S2
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
23-005038
Identifier Type: -
Identifier Source: org_study_id
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