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The Effect of a Planning Prompt on Seasonal Influenza Vaccination Rates

The Effect of a Planning Prompt on Seasonal Influenza Vaccination Rates

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01207232
Enrollment
3272
Registered
2010-09-22
Start date
2009-10-31
Completion date
2010-04-30
Last updated
2010-09-22

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, implementation intentions, planning prompt, nudge

Brief summary

The investigators conducted a 3-arm randomized controlled trial to test whether a low-cost planning intervention could increase influence vaccination rates.

Detailed description

Seasonal influenza causes 20,000 hospitalizations and 36,000 deaths in the U.S. each year. 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. This type of planning prompt is a nudge in the direction of desired behavior that can be implemented at minimal expense and does not restrict individual autonomy. We conducted a 3-arm randomized controlled trial to test whether a low-cost planning intervention could increase influence vaccination rates. We show that planning prompts can be successfully applied to improve health behaviors.

Interventions

BEHAVIORALPlanning Prompt

A prompt to write down a planned date (or date and time) for getting a flu shot

BEHAVIORALControl Condition

A basic reminder mailing prompted each subject to get their flu shot.

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Vaccine indications according to fall 2009 CDC criteria (age \>= 50 or chronic disease * Employee at partner corporation that implemented the study

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frame
Receipt of 2009 Seasonal Influenza Vaccinationup to 30 weeks

Countries

United States

Outcome results

None listed

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