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A Pilot Study Using Facebook to Support Opioid Recovery Among American Indian Women

Facebook Intervention for Preventing Opioid Relapse Among American Indian Women: Wiidookaage'Win Pilot Preparatory Study (Aim 1)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05340855
Enrollment
10
Registered
2022-04-22
Start date
2022-05-05
Completion date
2023-06-08
Last updated
2024-06-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Use

Keywords

American Indian, Alaska Native, Community Based Participatory Research

Brief summary

The purpose of this study is to develop a culturally relevant Facebook intervention for American Indian and Alaska Native (AIAN) women in Minnesota recovering from illicit opioid use.

Detailed description

This one-year, Phase I, pilot preparatory study aims to develop a culturally relevant Facebook intervention for American Indian and Alaska Native (AIAN) women in Minnesota recovering from illicit opioid use. The study will consist of three phases: (1) qualitative interviews, (2) intervention content refinement and a moderator exchange (i.e., bi-directional sharing of knowledge between intervention moderators and trainers), and (3) a beta-testing period. A study-specific Community Advisory Committee (CAC) was formed whose members contributed to the study protocol and will continue to provide guidance and input on the study implementation and dissemination. At the advice of the CAC, a Native Elder woman named the study. Wiidookaage'win is an Ojibwe word that means the place for help and time for helping, and reflects healing and community. The investigators expect the participatory approach to treatment development will result in a social media intervention with cultural relevance for Native women to maintain recovery from opioid use.

Interventions

A 30-day Facebook group prototype that is moderated by two women who will post various forms of media addressing opioid recovery, mindfulness, stress management, and resiliency.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Masking description

This is a single arm study where every participant in Phase 3 will receive the same single intervention.

Intervention model description

All study participants in Phase 3 beta test will be in the same Facebook group intervention and will view the same content.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

- Phase 1: AIAN Women: * AIAN based on self-reported race. * Gender identity as a woman. * Resides in Minnesota. * At least 18 years of age age with no upper age limit. * OUD based on the DSM-5 Checklist (American Psychiatric Association, 2013). * Self-reports at least one month of opioid abstinence based on Timeline Follow-Back (TLFB) interview. * Currently receiving MOUD. * Is comfortable speaking and reading English. * Is familiar with Facebook. * Has access to broadband internet on a mobile phone/computer/tablet at any location. AI/AN Health Care Providers and Stakeholders * Health care provider or AIAN community stakeholder. * Knowledge of Native culture and/or OUD treatment and recovery among AIAN people. * Is comfortable speaking and reading English. * Is familiar with Facebook. * Has access to broadband internet on a mobile phone/computer/tablet at any location. Having some familiarity with the Facebook platform is needed to provide feedback on content for a Facebook intervention. Access to the internet is needed to view online moderator postings for providing feedback during the interview. Inclusion Criteria - Phase 3: * AIAN person based on self-reported race/ethnicity. * Gender identity as a woman. * At least 18 years of age. * Resides in Minnesota. * 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. * Currently receiving 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 one month. * 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.

Exclusion criteria

AIAN potential participants in Phases 1 and 3 meeting any of the

Design outcomes

Primary

MeasureTime frameDescription
The Feasibility of Developing a Culturally Relevant Facebook Intervention30 daysThe number of times participants engaged with the Facebook page. Define by the total times of viewing, reacting, posting, commenting and voting on any Facebook post for all participants.

Secondary

MeasureTime frameDescription
The Feasibility of Using Facebook as an Opioid Intervention Platform30 daysThe number of participants who completed all study activities from baseline to end of study.
Treatment Satisfaction30 daysTreatment Satisfaction was measured using a 5-point Likert scale (1 = Strongly disagree, 5 = Strongly agree). Total scores range from 1 -5. Higher scores indicate greater satisfaction and lower scores indicate lower satisfaction.

Countries

United States

Participant flow

Participants by arm

ArmCount
Facebook Intervention
Subjects were emailed an invite link for the Facebook Intervention. Wiidookaage'win Facebook Group: A 30-day Facebook group prototype that was moderated by two women who posted various forms of media addressing opioid recovery, mindfulness, stress management, and resiliency.
10
Total10

Baseline characteristics

CharacteristicFacebook Intervention
Age, Continuous42.2 years
STANDARD_DEVIATION 12.82
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
10 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
8 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
2 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
0 Participants
Region of Enrollment
United States
10 participants
Sex: Female, Male
Female
10 Participants
Sex: Female, Male
Male
0 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 10
other
Total, other adverse events
0 / 10
serious
Total, serious adverse events
0 / 10

Outcome results

Primary

The Feasibility of Developing a Culturally Relevant Facebook Intervention

The number of times participants engaged with the Facebook page. Define by the total times of viewing, reacting, posting, commenting and voting on any Facebook post for all participants.

Time frame: 30 days

ArmMeasureValue (MEDIAN)
Facebook InterventionThe Feasibility of Developing a Culturally Relevant Facebook Intervention33.0 engagement events
Secondary

The Feasibility of Using Facebook as an Opioid Intervention Platform

The number of participants who completed all study activities from baseline to end of study.

Time frame: 30 days

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Facebook InterventionThe Feasibility of Using Facebook as an Opioid Intervention Platform9 Participants
Secondary

Treatment Satisfaction

Treatment Satisfaction was measured using a 5-point Likert scale (1 = Strongly disagree, 5 = Strongly agree). Total scores range from 1 -5. Higher scores indicate greater satisfaction and lower scores indicate lower satisfaction.

Time frame: 30 days

Population: One subject did not complete the post-intervention survey..

ArmMeasureValue (MEAN)Dispersion
Facebook InterventionTreatment Satisfaction4.84 score on a scaleStandard Deviation 0.18

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026