NCT05995886 · Mayo Clinic
Using Facebook to Support Opioid Recovery Among American Indian Women
What this study is about
The purpose of this study is to find out whether a Facebook group will help Native women in recovery from opioid use.
View original scientific description
The purpose of this study is to find out whether a Facebook group will help Native women in recovery from opioid use.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
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
Where
- Rochester, Minnesota
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced May 7, 2026 · Source of record for eligibility and locations