Recruiting NCT05995886
Using Facebook to Support Opioid Recovery Among American Indian Women
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Wiidookaage'win Facebook Group.
- Who it may be relevant to
- Registry conditions: Opioid Use Disorder. Basic parameters: from 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Facebook Intervention for Preventing Opioid Relapse Among American Indian Women: Wiidookaage'Win Pilot Preparatory Study (Aim 2)
Overview
The purpose of this study is to find out whether a Facebook group will help Native women in recovery from opioid use.
Interventions
- Behavioral Wiidookaage'win Facebook Group
An online social media group program that incorporates social support, mindfulness-based, and cultural practices that may support OUD recovery.
Primary outcome measures
- Feasibility of Facebook Intervention [Time frame: 3 months]
Secondary outcome measures (2)
- Timeline Follow-back Interview and UDS to measure Opioid Abstinence [Time frame: 6 months]
- Reporting MOUD continuation [Time frame: 6 months]
Eligibility criteria
Inclusion criteria
- AIAN person based on self-reported race/ethnicity
- Gender identity as a woman
- At least 18 years of age with no upper age limit
- Resides in Minnesota
- Meets criteria for OUD based on the DSM-5 Checklist (American Psychiatric Association, 2013)
- Self-reports at least one month of abstinence from opioid use based on TLFB interview and negative urine opiate screen
- Current use of MOUD
- Is comfortable speaking and reading English
- Has an existing Facebook account or willing to set one up
- Is willing and able to participate in the Facebook intervention for 3 months
- Has access to broadband internet on a mobile phone/computer/tablet at any location
- 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.
- Provides written informed consent
Exclusion criteria
- Self-reports current suicidality based on the Concise Heath Risk Tracking scale
- Participated in prior study phases (Aim 1 formative work) of NIDA CTN-0123
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 1 center
- Mayo Clinic — Rochester
Identifiers
NCT: NCT05995886 · 23-005038 · DA40316-08S2