Promoting Flu Vaccination Through a Mobile Wellness Program

October 20, 2016 updated by: Luca Foschini, Evidation Health

The investigators design a 6-week messaging campaign aimed at promoting flu vaccination among fully insured members of a national payer that participate in a wellness program offered by the insurer through a mobile app. Outcomes measured will include uptake in flu vaccination rate as measured by the insurer and engagement with the campaign through the app.

The goal of the research is to assess the effectiveness of pervasive computing messaging in promoting preventative care treatments such as flu shots. An additional goal is that of quantifying the importance of emphasizing incentives to increase efficacy of the messages.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

77983

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

    • California
      • Santa Barbara, California, United States, 93101
        • Evidation Health

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 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • belongs to fully insured population
  • continuous health coverage between January 1, 2015 and June 1, 2016
  • has downloaded and installed the wellness platform app

Exclusion Criteria:

  • has declined the messaging from the platform

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
Experimental: Salient

Messages in the salient arm highlight the number of incentives (points) received by getting a flu shot and recording it through the wellness program app.

Additionally, messages mention that flu shots can be received at the pharmacy while picking up an Rx.

Users in the arm are matched up with a second user from the same arm, randomly. For each pair, the messages are sent to both users at the same time within the specified time window. Such time is picked to be the day in which the first user is most likely to pick up an Rx from a pharmacy.

Short messages (100-250 characters) are to be delivered to a mobile app both by push notification (i.e., appearing on the phone dashboard like a text message if the user has allowed notifications from the app) and in-app messages (visible in the news feed of the wellness program app when the app is opened). Messages contain a short title (30 characters) and 2-3 lines of text in the body (30 characters each).
Active Comparator: NonSalient

Messages in the non-salient arm highlight the benefits of getting vaccinated against flu, but make no mention of incentives received for getting vaccinated.

Incentives would still be earned through the wellness program if the vaccination is recorded. Messages mention that flu shots can be received at the pharmacy while picking up an Rx.

Users in the arm are matched up with a second user from the same arm, randomly. For each pair, the messages are sent to both users at the same time within the specified time window. Such time is picked to be the day in which the first user is most likely to pick up an Rx from a pharmacy

Short messages (100-250 characters) are to be delivered to a mobile app both by push notification (i.e., appearing on the phone dashboard like a text message if the user has allowed notifications from the app) and in-app messages (visible in the news feed of the wellness program app when the app is opened). Messages contain a short title (30 characters) and 2-3 lines of text in the body (30 characters each).
No Intervention: Control
Users in this group will not receive any message promoting flu vaccination. Incentives would still be earned through the wellness program if the vaccination is recorded.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Increase in vaccination rate vs control
Time Frame: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in vaccination rate of anyone messaged relative to the control condition
Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in vaccination rate of salient vs non-salient
Time Frame: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in vaccination rate of those who received salient incentives messages vs those who received generic messages
Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Decrease in medically attended flu events of messaged vs control
Time Frame: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Decrease in observed flu rate for messaged users
Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in reporting of flu vaccination through wellness app of salient vs non-salient
Time Frame: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in reporting vaccination through the wellness program app following messages
Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in vaccination rate for users messaged within 2 days before of an expected rx pick-up.
Time Frame: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in vaccination rate of users messaged within 2 days before an expected Rx pick up from a pharmacy relative to their paired partners.
Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in message open rate of Salient vs Non-salient arm
Time Frame: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)
Increase in open rate of sent messages through the wellness program app of salient vs non salient arm
Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)

Collaborators and Investigators

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

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

September 1, 2016

Primary Completion (Anticipated)

December 1, 2016

Study Completion (Anticipated)

June 1, 2017

Study Registration Dates

First Submitted

September 9, 2016

First Submitted That Met QC Criteria

September 16, 2016

First Posted (Estimate)

September 21, 2016

Study Record Updates

Last Update Posted (Estimate)

October 21, 2016

Last Update Submitted That Met QC Criteria

October 20, 2016

Last Verified

October 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • EH-002

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

IPD Plan Description

Aggregated outcome data may be shared.

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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