- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04332614
Email Campaign to Increase Uptake of myGeisinger
Email Campaign to Encourage Patients to Complete Sign-up Process for Geisinger's Patient Portal
Study Overview
Status
Conditions
Detailed Description
Online patient portals are convenient tools that improve patient access to healthcare services while often reducing burden to both patients and providers. However, fewer than half of patients have enrolled in Geisinger's patient portal, myGeisinger.
The purpose of the current study is to assess what kind of messaging improves the effectiveness of an email campaign targeted at enrolling patients into Geisinger's online patient portal, called myGeisinger. Currently, Geisinger sends an email every month to patients who have started but not completed the enrollment process (they have had an activation code generated but have not yet used that code to enroll). This study will A/B test 5 email messages to assess if they perform better than the current standard email message.
Performance will be assessed based on whether patients open the email, click on the myGeisinger enrollment link, and enroll in myGeisinger. Statistical analyses will employ generalized linear models with a binary distribution and log-link function.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Danville, Pennsylvania, United States, 17822
- Geisinger
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Geisinger patients whose myGeisinger status is "Pending", meaning an activation code has been generated for them, but they have not completed activation
Exclusion Criteria:
- Patients without email addresses on file
- Patients who received emails from this monthly myGeisinger marketing campaign within the last 2 months
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Control
A standard marketing message encouraging activation and describing the benefits of myGeisinger
|
Email
|
|
Focused on provider communication
A simple message focused on one benefit of myGeisinger: communicating easily with providers
|
Email
|
|
Focused on scheduling
A simple message focused on one benefit of myGeisinger: scheduling and managing appointments online
|
Email
|
|
Focused on medical information access
A simple message focused on one benefit of myGeisinger: accessing medical information, like test results
|
Email
|
|
Social proof
A message similar to control, but including information about how many other patients are using myGeisinger
|
Email
|
|
Endowment / decision staging
A message similar to control, but framing myGeisinger as something that patients already have, and just need to take one more step to activate. Endowment: Give patients the impression they already have the account, so they value it more. Decision staging: Break down the process into multiple stages - "having" an account and "activating" that account- and giving the impression that they are almost there because the first stage is complete |
Email
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Email Opened: Control vs. Less-is-better vs. Social Proof vs. Endowment
Time Frame: 8-10 days post-intervention
|
Whether email was opened (yes / no)
|
8-10 days post-intervention
|
|
Link Clicked: Control vs. Less-is-better vs. Social Proof vs. Endowment
Time Frame: 8-10 days post-intervention
|
Whether the link / button to start the activation process was clicked (yes / no)
|
8-10 days post-intervention
|
|
Enrollment: Control vs. Less-is-better vs. Social Proof vs. Endowment
Time Frame: 8-10 days post-intervention
|
Whether the patient enrolled in myGeisinger (yes / no)
|
8-10 days post-intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Email Opened: Control vs. Less-is-better vs. Social Proof vs. Endowment
Time Frame: 32-35 days post-intervention
|
Whether email was opened (yes / no)
|
32-35 days post-intervention
|
|
Link Clicked: Control vs. Less-is-better vs. Social Proof vs. Endowment
Time Frame: 32-35 days post-intervention
|
Whether the link / button to start the activation process was clicked (yes / no)
|
32-35 days post-intervention
|
|
Enrollment: Control vs. Less-is-better vs. Social Proof vs. Endowment
Time Frame: 32-35 days post-intervention
|
Whether the patient enrolled in myGeisinger (yes / no)
|
32-35 days post-intervention
|
|
Email Opened: Within Less-is-better (Provider Communication vs. Managing Appointments vs. Medical Information Access)
Time Frame: 8-10 days post-intervention
|
Whether email was opened (yes / no)
|
8-10 days post-intervention
|
|
Link Clicked: Within Less-is-better (Provider Communication vs. Managing Appointments vs. Medical Information Access)
Time Frame: 8-10 days post-intervention
|
Whether the link / button to start the activation process was clicked (yes / no)
|
8-10 days post-intervention
|
|
Enrollment: Within Less-is-better (Provider Communication vs. Managing Appointments vs. Medical Information Access)
Time Frame: 8-10 days post-intervention
|
Whether the patient enrolled in myGeisinger (yes / no)
|
8-10 days post-intervention
|
|
Email Opened: Within Less-is-better (Provider Communication vs. Managing Appointments vs. Medical Information Access)
Time Frame: 32-35 days post-intervention
|
Whether email was opened (yes / no)
|
32-35 days post-intervention
|
|
Link Clicked: Within Less-is-better (Provider Communication vs. Managing Appointments vs. Medical Information Access)
Time Frame: 32-35 days post-intervention
|
Whether the link / button to start the activation process was clicked (yes / no)
|
32-35 days post-intervention
|
|
Enrollment: Within Less-is-better (Provider Communication vs. Managing Appointments vs. Medical Information Access)
Time Frame: 32-35 days post-intervention
|
Whether the patient enrolled in myGeisinger (yes / no)
|
32-35 days post-intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2020-0315
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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