The Effect of Time-Slot Scheduling on Flu Vaccination Rates
Effect of Time-Slot Scheduling on Flu Vaccination Rates
1 other identifier
interventional
50,000
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2009
Typical duration 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
September 1, 2009
CompletedFirst Submitted
Initial submission to the registry
September 14, 2010
CompletedFirst Posted
Study publicly available on registry
September 22, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2012
CompletedAugust 17, 2016
August 1, 2016
2.8 years
September 14, 2010
August 15, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Receipt of seasonal influenza vaccination
up to 30 weeks
Study Arms (5)
1 Hour Planning Prompt
EXPERIMENTAL2 Hour Planning Prompt
EXPERIMENTAL1 Day Planning Prompt
EXPERIMENTALDefault Planning Prompt
EXPERIMENTALControl
ACTIVE COMPARATORInterventions
Patients were prompted to write down a planned date (and in some cases time) for receiving a flu shot.
Patients were given a suggested date and time for receiving a flu shot.
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.
Eligibility Criteria
You may qualify if:
- seasonal influenza vaccine indications according to the CDC
- employees of partner corporations executing 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
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 14, 2010
First Posted
September 22, 2010
Study Start
September 1, 2009
Primary Completion
July 1, 2012
Study Completion
July 1, 2012
Last Updated
August 17, 2016
Record last verified: 2016-08