- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04587063
Evaluation of Emails Promoting Mail-order Pharmacy
October 26, 2020 updated by: Amir Goren, Geisinger Clinic
Evaluation of an Email Intervention Promoting Enrollment in Mail-order Pharmacy
In this evaluation, four versions of emails will be sent to eligible health plan members who are not currently enrolled in the health system's mail-order pharmacy.
A control group will not receive any communication.
The researchers hypothesize that the use of content informed by behavioral nudge theory in the emails should lead to increased enrollment in the health system's mail-order pharmacy.
Study Overview
Status
Completed
Conditions
Detailed Description
The utilization of a mail-order pharmacy can increase adherence to medications.
The health system's mail-order pharmacy (from here, simply referred to as mail-order pharmacy) can also provide reduced costs for medications.
Ongoing outreach efforts involve sending emails and other communications encouraging enrollment in Geisinger's mail-order pharmacy to eligible members of the system's health plan (i.e., those who take maintenance medications).
The study will compare a standard promotional email from these outreach efforts, as well as three new emails with content informed by behavioral science research, against a no-contact control arm and each other.
Study Type
Interventional
Enrollment (Actual)
5266
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
-
-
Pennsylvania
-
Danville, Pennsylvania, United States, 17822
- Geisinger
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- An active member of the health plan (Medicare, Commercial, or Exchange)
- Currently prescribed maintenance medications
- Not currently subscribed to the health system's mail-order pharmacy
- Has an email on record
Exclusion Criteria:
- Explicitly opted out of receiving emails from the health system
- Only has eligible current prescriptions for fewer than 28 days
- Only has prescriptions that cannot be sent via mail-order pharmacy (e.g., antidepressants, specialty-tier drugs)
- Is a Medicare member in the coverage gap
- Shares an email address with another selected participant (who was randomly chosen for inclusion among all those sharing the same email address)
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Standard Email
The "standard of care" email is the same as one used in prior outreach efforts at the health system, emphasizing reduced cost for medications and convenience.
|
Email
|
|
Experimental: Email with Healthcare Cost Savings
The email emphasizes future reductions in healthcare costs due to increased adherence with mail-order pharmacy, in addition to mentioning reduced prices for medications.
It also uses fear appeals by stating the risk of hospital stays and how mail-order pharmacy could be an easily-achievable way to avoid this negative consequence.
|
Email
Email
Email
|
|
Experimental: Email with Endorsement
The email is a letter from a doctor at the health system's health plan--who may been seen as a trusted source of information--encouraging the benefits of using a mail-order pharmacy.
|
Email
Email
|
|
Experimental: Email with Comparison Table
The email includes a table comparing the benefits and drawbacks of mail-order and chain pharmacies, which appeals to their sense of agency and allows them to make the choice that best suits them.
|
Email
Email
|
|
No Intervention: No Contact
Members do not receive an email.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mail-order Pharmacy Enrollment
Time Frame: 1 week from the intervention
|
Binary variable indicating if there was an enrollment in the health system's mail order pharmacy
|
1 week from the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Email Opens
Time Frame: 1 week from the intervention
|
Binary variable indicating if the email was opened
|
1 week from the intervention
|
|
Email Link Click
Time Frame: 1 week from the intervention
|
Binary variable indicating if the link to the mail-order pharmacy website was clicked
|
1 week from the intervention
|
|
Email Unsubscribes
Time Frame: 1 week from the intervention
|
Binary variable indicating if the recipient requested to unsubscribe from receiving emails from the health system
|
1 week from the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 13, 2020
Primary Completion (Actual)
October 20, 2020
Study Completion (Actual)
October 20, 2020
Study Registration Dates
First Submitted
October 6, 2020
First Submitted That Met QC Criteria
October 7, 2020
First Posted (Actual)
October 14, 2020
Study Record Updates
Last Update Posted (Actual)
October 27, 2020
Last Update Submitted That Met QC Criteria
October 26, 2020
Last Verified
October 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2020-0482 (Other Identifier: M D Anderson Cancer Center)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
Data with no personally identifiable information will be made available to other researchers on the Open Science Framework for transparency.
This will include the essential data and code needed to replicate the analysis that yielded reported findings.
The PI did not examine or analyze any data from this study prior to this registration.
IPD Sharing Time Frame
The data will become available after publication of study results in a scientific journal and will be available as long as the Open Science Framework hosts the data.
IPD Sharing Access Criteria
The data on the Open Science Framework will be open to anyone requesting that information.
IPD Sharing Supporting Information Type
- Study Protocol
- 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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