A Pilot Study Using Facebook to Support Opioid Recovery Among American Indian Women
- Conditions
- Opioid Use
- Interventions
- Behavioral: Wiidookaage'win Facebook Group
- Registration Number
- NCT05340855
- Lead Sponsor
- Mayo Clinic
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 10
Not provided
AIAN potential participants in Phases 1 and 3 meeting any of the exclusion criteria listed below will be excluded from study participation. Community stakeholder participants in - Phase 1 will only fail the screening if they meet the second exclusion criterion:
- Self-reports current suicidality.
- Inability or unwillingness of participant to provide verbal consent (Phase 1) or written informed consent (Phase 3).
- (Phase 3 only) Was a participant in Phase 1.
Pregnant women, lactating women, or women who plan to become pregnant will not be excluded because the treatment being evaluated is a behavioral intervention and does not involve medication or risk to the fetus.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Facebook Intervention Wiidookaage'win Facebook Group In Phase 3, all participants will receive the same intervention.
- Primary Outcome Measures
Name Time Method The Feasibility of Developing a Culturally Relevant Facebook Intervention 30 days 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.
- Secondary Outcome Measures
Name Time Method The Feasibility of Using Facebook as an Opioid Intervention Platform 30 days The number of participants who completed all study activities from baseline to end of study.
Treatment Satisfaction 30 days 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.
Trial Locations
- Locations (1)
Mayo Clinic Rochester
🇺🇸Rochester, Minnesota, United States