Using Facebook to Support Opioid Recovery Among American Indian Women

Opioid Use Disorder Clinical Trial

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05995886
• Other study ID #: 23-005038
• Secondary ID: DA40316-08S2
• Status: Recruiting
• Phase: N/A
• Start date: October 16, 2023
• Est. completion date: December 2024

Study information

• Verified date: October 2023
• Source: Mayo Clinic
• Contact: Antonia M Young, BA
• Phone: 1-833-880-2600
• Email: wiidookaagewin[@]mayo.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 2024
• Est. primary completion date: December 2024
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

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

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

Related Conditions & MeSH terms

• Opioid Use Disorder
• Opioid-Related Disorders

Intervention

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.

Locations

Country	Name	City	State
United States	Mayo Clinic	Rochester	Minnesota

Sponsors (2)

Lead Sponsor	Collaborator
Mayo Clinic	National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Perceived Stress Scale and Communal Mastery Scale	The study team will explore the differential impact of the intervention compared with the control condition on constructs targeted by our intervention, specifically perceived stress and coping with stressful life circumstances from a more collectivist orientation, respectively.	3 months
Primary	Feasibility of Facebook Intervention	The study team will measure the feasibility from the combined reports of recruitment, study retention, level of Facebook intervention uptake/engagement, and treatment satisfaction.	3 months
Secondary	Timeline Follow-back Interview and UDS to measure Opioid Abstinence	The study team will explore the preliminary differential impact of the intervention compared with the control condition on opioid abstinence and MOUD continuation. Opioid and other substance use will be assessed through monthly Timeline Follow-Back (TLFB) interviews (Sobell & Sobell, 1992; Wray et al., 2016). At 1, 3, and 6-months, the study team will obtain a UDS that will be used along with the TLFB interviews to measure opioid abstinence.	6 months
Secondary	Reporting MOUD continuation	The study team will summarize MOUD continuation as the proportion of participants reporting current use at 6-month follow-up.	6 months

External Links

•   Mayo Clinic Clinical Trials