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Not Condition-specificNCT02908893

Promoting Flu Vaccination Through a Mobile Wellness Program

A study testing In-app and push notification mobile messages in people with Not Condition-specific, run by Evidation Health at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Not Condition-specific
What is being tested?
In-app and push notification mobile messages
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50,286 participants
Where
1 siteUnited States
Study dates
Sep 2016to Jun 2017
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • has declined the messaging from the platform

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Evidation Health

    Santa Barbara, California, 93101

Other trials in United States

About this study

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.

Being tested
In-app and push notification mobile messages

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • In-app and push notification mobile messagesBehavioural

    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).

Study groups in NCT02908893
Study groupRoleWhat they receive
SalientExperimentalMessages 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.
Receives: Behavioral: In-app and push notification mobile messages
NonSalientActive comparatorMessages 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
Receives: Behavioral: In-app and push notification mobile messages
ControlNo interventionUsers 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 being measured

The primary outcome is the main question the study is designed to answer.

  1. Increase in vaccination rate vs control

    Increase in vaccination rate of anyone messaged relative to the control condition

    Measured: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)

  2. Increase in vaccination rate of salient vs non-salient

    Increase in vaccination rate of those who received salient incentives messages vs those who received generic messages

    Measured: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)

Secondary outcomes (4)
  1. Decrease in medically attended flu events of messaged vs control

    Decrease in observed flu rate for messaged users

    Measured: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)

  2. Increase in reporting of flu vaccination through wellness app of salient vs non-salient

    Increase in reporting vaccination through the wellness program app following messages

    Measured: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)

  3. Increase in vaccination rate for users messaged within 2 days before of an expected rx pick-up.

    Increase in vaccination rate of users messaged within 2 days before an expected Rx pick up from a pharmacy relative to their paired partners.

    Measured: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)

  4. Increase in message open rate of Salient vs Non-salient arm

    Increase in open rate of sent messages through the wellness program app of salient vs non salient arm

    Measured: Up to 1 week after the end of each of the three batches of the intervention (Oct 1/15/28 2016)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Sep 2016 (estimated)
  2. Study startSep 2016
  3. Primary completionDec 2016
  4. Study completionJun 2017

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
50,286 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02908893
Sponsor's protocol ID
EH-002
Status last verified
Sep 2026
First submitted
9 Sep 2016
Last updated
18 Sep 2026
Results posted
No
Data monitoring committee
No
Individual data sharing
Undecided: Aggregated outcome data may be shared.

Publications

  • Lee WN, Stuck D, Konty K, Rivers C, Brown CR, Zbikowski SM, Foschini L. Large-scale influenza vaccination promotion on a mobile app platform: A randomized controlled trial. Vaccine. 2020 Apr 16;38(18):3508-3514. doi: 10.1016/j.vaccine.2019.11.053. Epub 2019 Nov 29.

    PubMed 31787410

Questions about this trial

What is this clinical trial studying?

A study testing In-app and push notification mobile messages in people with Not Condition-specific, run by Evidation Health at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02908893, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Sep 2026.

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