- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02411032
Fresh Start Experiment
May 2, 2017 updated by: Katherine Milkman, University of Pennsylvania
The investigators are proposing an experiment to help Humana investigate when to launch programs or send messages that are designed to improve customers' engagement.
The investigators' past research has shown that certain life events and calendar events (e.g., a job change, a birthday, a holiday, Monday) feel like a "fresh start" to people and have the potential to motivate them to begin pursuing their health goals (e.g., exercising, starting a diet, quitting smoking).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The investigators are proposing an experiment to help Humana investigate when to launch programs or send messages that are designed to improve customers' engagement.
The investigators' past research has shown that certain life events and calendar events (e.g., a job change, a birthday, a holiday, Monday) feel like a "fresh start" to people and have the potential to motivate them to begin pursuing their health goals (e.g., exercising, starting a diet, quitting smoking).
In this experiment, the investigators will test (a) whether Humana can increase the effectiveness of its messages by sending them to customers around fresh starts moments and (b) whether highlighting a recent fresh start event in Humana's messages can further increase customer engagement.
Study Type
Interventional
Enrollment (Actual)
13323
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
-
Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania
-
-
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:
- customers of our insurance company partner
Exclusion Criteria:
- none
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: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Reminder control
Customers receive a mailing on a random day, which does not coincide with any of the predictable fresh start events.
|
Customer gets mailing that reminds them to take their medication.
|
Experimental: Birthday framed
Customers receive a mailing on the most recent Wednesday before the customers' birthday, and the mailing frames the customers' birthday by emphasizing a fresh start associated with the customers' birthday.
|
Customers receive a mailing around a fresh start event: New Year's or birthday
The fresh start event will be highlighted in the mailings.
|
Experimental: New Year's framed
Customers receive a mailing on 1/21/15, and the mailing frames the customers' birthday by emphasizing a fresh start associated with the customers' birthday.
|
Customers receive a mailing around a fresh start event: New Year's or birthday
The fresh start event will be highlighted in the mailings.
|
Experimental: Birthday un-framed
Customers receive a mailing on the most recent Wednesday before the customers' birthday, but the mailing does not frame the customers' birthday.
|
Customers receive a mailing around a fresh start event: New Year's or birthday
|
Experimental: New Year's un-framed
Customers receive a mailing on 1/21/15, but the mailing does not frame New Year's.
|
Customers receive a mailing around a fresh start event: New Year's or birthday
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Medication refills
Time Frame: 6 months
|
frequency of refilling medication
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Hemoglobin A1C
Time Frame: 6 months
|
6 months
|
LDL cholesterol
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Katherine Milkman, Ph.D, University of Pennsylvania
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
April 1, 2015
Primary Completion (Actual)
October 1, 2015
Study Completion (Actual)
October 1, 2015
Study Registration Dates
First Submitted
April 3, 2015
First Submitted That Met QC Criteria
April 7, 2015
First Posted (Estimate)
April 8, 2015
Study Record Updates
Last Update Posted (Actual)
May 3, 2017
Last Update Submitted That Met QC Criteria
May 2, 2017
Last Verified
May 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 820768
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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