A nudge in the mailbox: could a letter boost flu shots for millions at risk?
NCT ID NCT07798882
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This trial tests whether mailed letters, patient portal messages, or texts can encourage flu vaccination among adults with multiple risk factors for severe influenza. Researchers will identify high-risk patients using a simple rule-based scoring system, then send reminders and track whether they get a flu shot. The goal is to see if low-cost, non-algorithmic nudges can improve vaccination rates in a vulnerable population.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Behavioral intervention: mailed letter, patient portal message, and/or text message reminding high-risk patients to get a flu shot
- What this could lead to
- If effective, simple reminders could significantly increase flu vaccination rates among vulnerable adults, reducing flu-related hospitalizations and complications.
- What could go wrong
- The trial is early and relies on voluntary behavior change; reminders may not sway everyone, and results may vary across different patient groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 51,215 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18 or older * Has four or more CDC risk factors for influenza reflected in EHR data * Has a primary care physician employed by Geisinger * Attended at least one appointment at Geisinger between 7/17/2024 and 7/16/2026 * Attended at least one primary care appointment at Geisinger between 10/1/2008 and 7/16/2026 Exclusion criterion: \- Attended an appointment at Community Care between 9/1/2024 and 7/16/2026
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Geisinger Health
Danville, Pennsylvania, 17822, United States
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