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Mobile Health-based Motivational Interviewing to Promote COVID-19 Vaccination

Not Applicable
Completed
Conditions
Vaccination Hesitancy
Registration Number
NCT05977192
Lead Sponsor
Oklahoma State University
Brief Summary

The objective of this study is to evaluate the preliminary efficacy and acceptability of an mobile Health-based motivational interviewing (MI) intervention to promote SARS-CoV-2 vaccination (MOTIVACC) compared to traditional phone-based MI.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • >18 years
  • Reside in a rural area
  • No previous dose of a SARS-CoV-2 vaccine
  • Speak English
  • Able to provide informed consent
Exclusion Criteria
  • A cognitive or other disability that inhibits smart phone use
  • Inability to participate because of medical or psychiatric conditions diagnosed by a physician/clinician
  • Enrollment in other COVID-19 research; pregnant or lactating

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Changes in vaccine hesitancy and confidenceBaseline and follow-up (8 weeks)
Changes in intention to receive the vaccineBaseline and follow-up (8 weeks)
Secondary Outcome Measures
NameTimeMethod
Number of participants who receive the COVID-19 vaccineFollow-up (8 weeks)
Changes in self-efficacyBaseline and follow-up (8 weeks)
Changes in ambivalenceBaseline and follow-up (8 weeks)
Changes in value-behavior discrepancyBaseline and follow-up (8 weeks)
Changes in expectations related to vaccinesBaseline and follow-up (8 weeks)

Trial Locations

Locations (2)

University of Oklahoma

🇺🇸

Oklahoma City, Oklahoma, United States

Oklahoma State University

🇺🇸

Stillwater, Oklahoma, United States

University of Oklahoma
🇺🇸Oklahoma City, Oklahoma, United States

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