Using Facebook to Support Opioid Recovery Among American Indian Women

NCT ID: NCT05995886

Last Updated: 2026-01-21

Study Results

Results pending

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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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-16

Study Completion Date

2026-07-31

Brief Summary

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

Detailed Description

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Conditions

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Opioid Use Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

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.

Group Type EXPERIMENTAL

Wiidookaage'win Facebook Group

Intervention Type BEHAVIORAL

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.

Group Type NO_INTERVENTION

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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion 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

Exclusion Criteria

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
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Christi Patten

Professor of Psychology

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status RECRUITING

Countries

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United States

Central Contacts

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Ashley Brown

Role: CONTACT

1-833-880-2600

Facility Contacts

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Corinna Sabaque

Role: primary

833-880-2600

Related Links

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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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