The Effect of a Planning Prompt on Seasonal Influenza Vaccination Rates
1 other identifier
interventional
3,272
1 country
1
Brief Summary
The investigators conducted a 3-arm randomized controlled trial to test whether a low-cost planning intervention could increase influence vaccination rates.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2009
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2010
CompletedFirst Submitted
Initial submission to the registry
September 20, 2010
CompletedFirst Posted
Study publicly available on registry
September 22, 2010
CompletedSeptember 22, 2010
September 1, 2010
1 month
September 20, 2010
September 21, 2010
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Receipt of 2009 Seasonal Influenza Vaccination
up to 30 weeks
Study Arms (3)
Time Plan Condition
EXPERIMENTALA basic reminder mailing prompted each subject to write down a planned date and time for getting their flu shot.
Date Plan Condition
EXPERIMENTALA basic reminder mailing prompted each subject to write down a planned date for getting their flu shot.
Control Condition
ACTIVE COMPARATORA basic reminder mailing prompted each subject to receive a flu shot.
Interventions
A prompt to write down a planned date (or date and time) for getting a flu shot
A basic reminder mailing prompted each subject to get their flu shot.
Eligibility Criteria
You may qualify if:
- Vaccine indications according to fall 2009 CDC criteria (age \>= 50 or chronic disease
- Employee at partner corporation that implemented the study
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Pennsylvanialead
- Harvard Universitycollaborator
- Yale Universitycollaborator
- Stanford Universitycollaborator
Study Sites (1)
University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Katherine L Milkman, Ph.D.
University of Pennsylvania
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
September 20, 2010
First Posted
September 22, 2010
Study Start
October 1, 2009
Primary Completion
November 1, 2009
Study Completion
April 1, 2010
Last Updated
September 22, 2010
Record last verified: 2010-09