Non-integrated Costs Increase Effectiveness of Incentives

April 23, 2018 updated by: Carnegie Mellon University

The investigators will test the hypothesis that the control (no incentive) condition will have the lowest vaccination rate, the main task condition will have a significantly higher vaccination rate while the indirect condition will have the highest vaccination rate.

Participants will be randomly assigned to one of the three message conditions and their vaccination records obtained from the university Occupational Health Department.

Study Overview

Detailed Description

The investigators will send e-mails to a complete mailing list of faculty and staff at a university. Each recipient will be randomly assigned to one of three conditions: control, main task incentive or indirect incentive. Our main dependent variable will be whether or not participants decide to get vaccinated. The investigators will obtain their actual vaccination records from the university Occupational Health Department.

Within the e-mail message, participants will indicate whether or not they intend to get vaccinated. Intention serves as an indirect dependent outcome. Upon clicking to indicate their intention, participants are redirected to a page which gives further instructions on how to proceed.

Participants who vaccinate will be asked to complete a brief follow-up questionnaire to evaluate their experience with vaccination and (for those offered and incentive) to provide contact information to receive their payment.

Study Type

Interventional

Enrollment (Actual)

12531

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New Jersey
      • New Brunswick, New Jersey, United States, 08901
        • Rutgers University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 100 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Must be faculty or staff at Rutgers University.

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Control
Participants will receive an E-mail Message encouraging them to get vaccinated, and asking them to indicate if they intend to do so and to complete a brief questionnaire after vaccination.
Participants will randomly receive an e-mail message about the availability of free flu vaccines.
Experimental: Direct Incentive
Participants will receive an E-mail Message encouraging them to get vaccinated, and asking them to indicate if they intend to do so and to complete a brief questionnaire after vaccination. They are offered an Incentive for Vaccination ($5 Amazon Gift Card).
Participants will randomly receive an e-mail message about the availability of free flu vaccines.
$5 gift card offered for vaccination
Experimental: Indirect Incentive
Participants will receive an E-mail Message encouraging them to get vaccinated, and asking them to indicate if they intend to do so and to complete a brief questionnaire after vaccination. They are offered an Incentive for completing a short survey ($5 Amazon Gift Card).
Participants will randomly receive an e-mail message about the availability of free flu vaccines.
$5 gift card offered for completing s short survey after one gets vaccinated

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of people vaccinated
Time Frame: Up to 5 months
Measure the number of people who got vaccinated in the Fall 2017 semester at a large state university. We will collect vaccination records from the university Occupational Health Department
Up to 5 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intention to get vaccinated
Time Frame: Up to 5 months
Participants will receive an e-mail with our main treatment manipulations. In each e-mail they will be able to indicate whether or not they want to get vaccinated. We will use this measure as a second dependent variable.
Up to 5 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: George Loewenstein, PhD, Carnegie Mellon University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 20, 2017

Primary Completion (Actual)

January 20, 2018

Study Completion (Actual)

January 20, 2018

Study Registration Dates

First Submitted

January 24, 2018

First Submitted That Met QC Criteria

April 23, 2018

First Posted (Actual)

April 25, 2018

Study Record Updates

Last Update Posted (Actual)

April 25, 2018

Last Update Submitted That Met QC Criteria

April 23, 2018

Last Verified

April 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • P30AG0345462017

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified data (condition, vaccination status) will be shared on a site such as Open Science Framework

IPD Sharing Time Frame

12/31/2019, indefinitely

IPD Sharing Access Criteria

open access

IPD Sharing Supporting Information Type

  • ANALYTIC_CODE

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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