The Effect of a Planning Prompt on Seasonal Influenza Vaccination Rates
- Conditions
- Seasonal Influenza
- Interventions
- Behavioral: Planning PromptBehavioral: Control Condition
- Registration Number
- NCT01207232
- Lead Sponsor
- University of Pennsylvania
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 3272
- Vaccine indications according to fall 2009 CDC criteria (age >= 50 or chronic disease
- Employee at partner corporation that implemented the study
- None
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Time Plan Condition Planning Prompt A basic reminder mailing prompted each subject to write down a planned date and time for getting their flu shot. Date Plan Condition Planning Prompt A basic reminder mailing prompted each subject to write down a planned date for getting their flu shot. Control Condition Control Condition A basic reminder mailing prompted each subject to receive a flu shot.
- Primary Outcome Measures
Name Time Method Receipt of 2009 Seasonal Influenza Vaccination up to 30 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States