CONFIDENT: A Randomized Trial to Increase COVID-19 Vaccine Confidence in Long-term Care Workers
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,634
- 试验地点
- 2
- 主要终点
- COVID-19 Vaccine Confidence
研究概览
简要总结
The CONFIDENT Study is an online three-arm randomized trial that aims to help long-term care workers in the United States feel more confident about the Coronavirus Disease 2019 (COVID-19) vaccines. The study will compare two different interventions to usual online information (website of the Centers for Disease Control and Prevention). The first intervention is a Dialogue-Based Webinar where people can interact and ask questions about the vaccines. The second intervention is a Social Media Website that will feature curated content about the vaccines from popular social media platforms.
Participants will be asked to completed four online surveys. The first survey will be completed pre-intervention and immediately upon study enrollment (Time 0). Participants will be randomized to a trial arm at the end of the Time 0 survey. Intervention follow-up surveys will be completed 3 weeks post-randomization (Time 1), three months post-randomization (Time 2), and 6 months post-randomization (Time 3).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •at least 18 years of age
- •can read, write, and understand English
- •lives in the United States
- •has worked in a long-term care setting in the past two years
- •can provide information to confirm they have worked in a long-term care setting
- •is not pregnant or breastfeeding
- •at least somewhat worried about the COVID-19 vaccines and/or has not received a COVID-19 vaccine booster shot
排除标准
- •under 18 years of age
- •cannot read, write, and understand English
- •does not live in the United States
- •has not worked in a long-term care setting in the past two years
- •cannot provide information to confirm they have worked in a long-term care setting
- •is pregnant or breastfeeding
- •less than somewhat worried about the COVID-19 vaccines and has received at least one COVID-19 vaccine booster shot
结局指标
主要结局
COVID-19 Vaccine Confidence
时间窗: 3 weeks post-randomization (Time 1)
Confidence in the COVID-19 vaccines, assessed using the 3-item Vaccine Confidence Index (Larson et al., 2016) adapted for COVID-19. Each item is rated on a 5-point scale ranging from 1 ('Strongly disagree') to 5 ('Strongly agree'). Respondents are considered 'confident' (score of '1') if they respond 'Agree' or 'Strongly agree' on all three items and 'not confident' (score of '0') if one or more item responses is not 'Agree' or 'Strongly agree'.
次要结局
- Change From Baseline to 3 Weeks Post-randomization in COVID-19 Vaccine Confidence(Baseline (Time 0); 3 weeks post-randomization (Time 1))
- Change From Baseline to 3 Months Post-randomization in COVID-19 Vaccine Confidence(Baseline (Time 0); 3 months post-randomization (Time 2))
- Change From Baseline to 6 Months Post-randomization in COVID-19 Vaccine Confidence(Baseline (Time 0); 6 months post-randomization (Time 3))
- Net Promoter Score (COVID-19 Vaccination)(3 weeks post-randomization (Time 1))
- Net Promoter Score (COVID-19 Booster Vaccination to Coworker)(3 weeks post-randomization (Time 1))
- COVID-19 Vaccine Uptake (Any Dose)(3 weeks post-randomization (Time 1))
- COVID-19 Vaccine Uptake (Initial Series Completion)(3 weeks post-randomization (Time 1))
- COVID-19 Vaccine Uptake (Booster Completion)(3 weeks post-randomization (Time 1))
- COVID-19 Vaccine Intent (Future Vaccine Recommendations)(3 weeks post-randomization (Time 1))
- COVID-19 Vaccine Intent (Initial Series)(3 weeks post-randomization (Time 1))
- COVID-19 Vaccine Intent (Booster)(3 weeks post-randomization (Time 1))
- Feeling Informed About the COVID-19 Vaccines(3 weeks post-randomization (Time 1))
- Identification of COVID-19 Vaccine Information and Misinformation(3 weeks post-randomization (Time 1))
- Trust in COVID-19 Vaccine Information From Different Sources(3 weeks post-randomization (Time 1))
- Change From Baseline in Secondary Outcomes(Baseline (Time 0); 3 weeks post-randomization (Time 1); 3 months post-randomization (Time 2); 6 months post-randomization (Time 3))
- As-treated Analyses of Primary and Secondary Outcomes(Baseline (Time 0); 3 weeks post-randomization (Time 1); 3 months post-randomization (Time 2); 6 months post-randomization (Time 3))
研究者
Glyn Jones-Elwyn
Professor
Dartmouth-Hitchcock Medical Center