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The Effect of Time-Slot Scheduling on Flu Vaccination Rates

Effect of Time-Slot Scheduling on Flu Vaccination Rates

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01206686
Enrollment
50000
Registered
2010-09-22
Start date
2009-09-30
Completion date
2012-07-31
Last updated
2016-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Seasonal Influenza

Keywords

seasonal influenza, behavioral economics, nudge, implementations intentions, vaccination

Brief summary

The goal of this project is to see if encouraging an individual to privately choose in advance a narrow time window in which to obtain a flu vaccination shot affects the likelihood that he or she will become vaccinated.

Detailed description

Influenza causes 36,000 U.S. deaths per year, but influenza immunization rates average just 28%. Behavioral nudges may increase the effectiveness of immunization reminder mailers at little or no added cost. Past psychology research has demonstrated that prompting people to form an implementation plan of the form, When situation x arises, I will implement response y, increases attainment of desired goals because the desired behavior is linked to a concrete future moment. We study whether adding a planning prompt to a vaccination reminder mailer increases immunization rates.

Interventions

BEHAVIORALPlanning Prompt

Patients were prompted to write down a planned date (and in some cases time) for receiving a flu shot.

BEHAVIORALDefault Appointment

Patients were given a suggested date and time for receiving a flu shot.

BEHAVIORALControl

Patients were provided with basic information (present in all conditions) about when and where they could receive a flu shot, but they were given no further treatment.

Sponsors

Harvard University
CollaboratorOTHER
Yale University
CollaboratorOTHER
Stanford University
CollaboratorOTHER
University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* seasonal influenza vaccine indications according to the CDC * employees of partner corporations executing study

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frame
Receipt of seasonal influenza vaccinationup to 30 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026