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Informational Interventions for COVID-19 Booster Uptake

N/A
Recruiting
Research Sponsored by University of California, Los Angeles
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Patients aged 18 or above
Having completed a COVID-19 vaccine primary series based on CAIR data
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 week after getting the text message
Awards & highlights

Study Summary

This trial looks into how text reminders can increase people's desire to get the COVID-19 booster shot. The study will assess how info & consistency can improve uptake.

Who is the study for?
This trial is for adults aged 18 or older who have completed their initial COVID-19 vaccine series and haven't had a booster in at least two months. They must have an SMS-capable phone number registered with UCLA Health but can't join if they've already scheduled or received the bivalent booster.Check my eligibility
What is being tested?
The study tests whether text reminders that provide information about COVID-19, emphasize consistency with past actions, and explain the uniqueness and eligibility for the bivalent booster can increase people's intentions to get this updated shot.See study design
What are the potential side effects?
Since this trial focuses on communication strategies rather than medical interventions, there are no direct side effects from participating. However, general side effects of COVID-19 boosters may include sore arm, fatigue, fever.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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You are 18 years old or older.
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You have completed the full series of COVID-19 vaccination.
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You must have received your last COVID-19 vaccine (including booster) at least two months before the trial starts. This is to make sure you're eligible for the updated booster.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 week after getting the text message
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 week after getting the text message for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Secondary Immunization
Secondary Immunization
Secondary outcome measures
Link click rate in 1 week

Trial Design

7Treatment groups
Experimental Treatment
Active Control
Group I: Uniqueness information reminderExperimental Treatment2 Interventions
Group II: Simple reminderExperimental Treatment1 Intervention
Group III: Severity information reminderExperimental Treatment2 Interventions
Group IV: Eligibility information reminderExperimental Treatment2 Interventions
Group V: Consistency reminderExperimental Treatment2 Interventions
Group VI: Consistency and uniqueness information reminderExperimental Treatment3 Interventions
Group VII: HoldoutActive Control1 Intervention

Find a Location

Who is running the clinical trial?

University of California, Los AngelesLead Sponsor
1,521 Previous Clinical Trials
10,118,936 Total Patients Enrolled

Media Library

Severity information reminder Clinical Trial Eligibility Overview. Trial Name: NCT05586178 — N/A
Coronavirus Research Study Groups: Severity information reminder, Holdout, Consistency reminder, Eligibility information reminder, Simple reminder, Uniqueness information reminder, Consistency and uniqueness information reminder
Coronavirus Clinical Trial 2023: Severity information reminder Highlights & Side Effects. Trial Name: NCT05586178 — N/A
Severity information reminder 2023 Treatment Timeline for Medical Study. Trial Name: NCT05586178 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there still openings available to participate in this clinical research?

"According to the clinicaltrials.gov webpage, the recruitment process for this study is currently underway. It was published on October 18th 2022 and last edited November 8th 2022."

Answered by AI

How many participants is the research team enrolling in this investigation?

"Affirmative. According to clinicaltrials.gov, the medical trial posted on October 18th 2022 is actively seeking volunteers for its study. The research project plans to enrol 160,000 participants from one location."

Answered by AI

Who else is applying?

What state do they live in?
Florida
District of Columbia
Other
California
What portion of applicants met pre-screening criteria?
Did not meet criteria
Met criteria
What site did they apply to?
UCLA Health Department of Medicine, Quality Office
How many prior treatments have patients received?
0
1
~66207 spots leftby Mar 2025