CONFIDENT: Supporting Long-term Care Workers During COVID-19

Dartmouth Health

Status: Completed

Conditions: COVID-19

Treatments: Behavioral: Dialogue-Based Webinar; Other: Enhanced Usual Practice; Behavioral: Social Media Website

Study type: Interventional

Funder types: Other

Identifiers

NCT05168800

STUDY00032340

Details and patient eligibility

About

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).

Enrollment: 2,634 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 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

Exclusion criteria

• 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

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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2,634 participants in 3 patient groups

Dialogue-Based Webinar

Experimental group

Treatment:

Behavioral: Dialogue-Based Webinar

Social Media Website

Experimental group

Treatment:

Behavioral: Social Media Website

Enhanced Usual Practice

Active Comparator group

Treatment:

Other: Enhanced Usual Practice