Abstract
BACKGROUND: Seasonal influenza affects 5% to 15% of Americans annually, resulting in preventable deaths and substantial economic impact. Influenza infection is particularly dangerous for people with cardiovascular disease, who therefore represent a priority group for vaccination campaigns.
OBJECTIVE: We aimed to assess the effects of digital intervention messaging on self-reported rates of seasonal influenza vaccination.
METHODS: This was a randomized, controlled, single-blind, and decentralized trial conducted at individual locations throughout the United States over the 2020-2021 influenza season. Adults with self-reported cardiovascular disease who were members of the Achievement mobile platform were randomized to receive or not receive a series of 6 patient-centered digital intervention messages promoting influenza vaccination. The primary end point was the between-group difference in self-reported vaccination rates at 6 months after randomization. Secondary outcomes included the levels of engagement with the messages and the relationship between vaccination rates and engagement with the messages. Subgroup analyses examined variation in intervention effects by race. Controlling for randomization group, we examined the impact of other predictors of vaccination status, including cardiovascular condition type, vaccine drivers or barriers, and vaccine knowledge.
RESULTS: Of the 49,138 randomized participants, responses on the primary end point were available for 11,237 (22.87%; 5575 in the intervention group and 5662 in the control group) participants. The vaccination rate was significantly higher in the intervention group (3418/5575, 61.31%) than the control group (3355/5662, 59.25%; relative risk 1.03, 95% CI 1.004-1.066; P=.03). Participants who were older, more educated, and White or Asian were more likely to report being vaccinated. The intervention was effective among White participants (P=.004) but not among people of color (P=.42). The vaccination rate was 13 percentage points higher among participants who completed all 6 intervention messages versus none, and at least 2 completed messages appeared to be needed for effectiveness. Participants who reported a diagnosis of COVID-19 were more likely to be vaccinated for influenza regardless of treatment assignment.
CONCLUSIONS: This personalized, evidence-based digital intervention was effective in increasing vaccination rates in this population of high-risk people with cardiovascular disease.
TRIAL REGISTRATION: ClinicalTrials.gov NCT04584645; https://clinicaltrials.gov/ct2/show/NCT04584645.
Original language | English (US) |
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Article number | e38710 |
Journal | Journal of medical Internet research |
Volume | 24 |
Issue number | 10 |
DOIs | |
State | Published - Oct 1 2022 |
Externally published | Yes |
Bibliographical note
Funding Information:This study was funded by Sanofi. This sponsor was involved in the intervention development, study design, data interpretation, and writing of the report and was kept informed during data collection and data analysis. Sanofi produces one of the influenza vaccines available in the United States, but participants were not instructed to get a specific type of influenza vaccine. The senior (SS) and corresponding (NJM) authors had full access to all of the data in the study and had final responsibility for the decision to submit for publication. The authors thank Patricia A. French, BS, of Left Lane Communications for assistance in the drafting and editing of the manuscript.
Publisher Copyright:
© 2022 Journal of Medical Internet Research. All rights reserved.
Keywords
- cardiovascular disease
- digital intervention
- digital messaging
- immunization
- influenza
- mHealth
- mobile health
- public health
- randomized trial
- vaccination
- Single-Blind Method
- Influenza Vaccines/therapeutic use
- Cardiovascular Diseases/prevention & control
- United States
- Humans
- Influenza, Human/epidemiology
- Vaccination
- COVID-19
- Text Messaging
- Adult
PubMed: MeSH publication types
- Randomized Controlled Trial
- Journal Article
- Research Support, Non-U.S. Gov't