Assessing the Impact of myHealth Rewards Enrollment Emails
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ClinicalTrials.gov Identifier: NCT03965754 |
Recruitment Status :
Completed
First Posted : May 29, 2019
Results First Posted : October 5, 2020
Last Update Posted : December 7, 2020
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Condition or disease | Intervention/treatment |
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Health Promotion Wellness Programs | Behavioral: Social norms Behavioral: Loss framing Behavioral: Email reminder |
Study Type : | Observational |
Actual Enrollment : | 5697 participants |
Observational Model: | Case-Control |
Time Perspective: | Prospective |
Official Title: | Assessing the Impact of myHealth Rewards Program-related Email Communications on Enrollment |
Actual Study Start Date : | May 7, 2019 |
Actual Primary Completion Date : | May 14, 2019 |
Actual Study Completion Date : | May 14, 2019 |
Group/Cohort | Intervention/treatment |
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No email
No email will be sent out to this subset of GHP members during the week that the other emails are sent.
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Standard email reminder
The standard email reminder mentions the average premium savings, the speed and ease of starting the process, and the deadline for registering and having health measures on file, plus it provides two button links for registering and finding free health screenings where health measures can be collected and registered at one convenient time and location.
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Behavioral: Email reminder
This intervention is a standard email reminder that mentions the average premium savings, the speed and ease of starting the process, and the deadline for registering and having health measures on file, plus it provides two button links for registering and finding screenings. |
Social norms email
The social norms email notes that a majority (78%) of GHP members' colleagues had enrolled in 2018, it provides a testimonial from a medical director at Geisinger's Commonwealth School of Medicine, stating the ways in which myHealth Rewards helped that doctor personally, and it emphasizes the simplicity and ease of taking the first step toward enrollment.
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Behavioral: Social norms
This intervention introduces recipients to descriptive social norms specifying that a majority of their colleagues have signed up for the program, which sets a normative standard against which recipients are expected to compare themselves and to change their behavior accordingly (i.e., when they realize that their behavior is discrepant from that of relevant others). The personal testimonial from a Geisinger medical director serves as a personal exemplar intended to further enhance the effect of the social norms with an implicit indication that the intended behavior is desirable and feasible.
Other Names:
Behavioral: Email reminder This intervention is a standard email reminder that mentions the average premium savings, the speed and ease of starting the process, and the deadline for registering and having health measures on file, plus it provides two button links for registering and finding screenings. |
Loss framing
The loss framing email suggests that GHP members are currently "throwing away" a precise dollar amount (over $2,000) by not participating and that they can therefore avoid missing out on substantial gains (i.e., savings) by taking action.
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Behavioral: Loss framing
This intervention frames the status quo as a state from which recipients, via inaction, are slated to forfeit a sizable and precise monetary amount to which they should otherwise feel entitled (via loss aversion and the endowment effect). People tend to be risk-seeking in the domain of losses; therefore, this intervention is hypothesized to increase enrollment in the hope of achieving zero loss by meeting program goals, as opposed to a sure loss via inaction.
Other Name: Endowment effect Behavioral: Email reminder This intervention is a standard email reminder that mentions the average premium savings, the speed and ease of starting the process, and the deadline for registering and having health measures on file, plus it provides two button links for registering and finding screenings. |
- Enrollment (7 Days) [ Time Frame: 7 days, from May 7 through 13, 2019 ]Enrollment in the myHealth Rewards program (yes/no) within 7 full days of the beginning of the intervention (i.e., when the emails are first sent).
- Logging in (7 Days) [ Time Frame: 7 days, from May 7 through 13, 2019 ]Logging into the myHealth Rewards program (yes/no) within 7 full days of the beginning of the intervention.

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Probability Sample |
Inclusion Criteria:
- Geisinger employees who are benefits subscribers
Exclusion Criteria:
- Those who had already registered for myHealth Rewards in 2019, up through May 6, 2019
- New Geisinger employees hired between December 1, 2018 and May 6, 2019
- Existing Geisinger employees who transitioned from non-subscribers in 2018 to subscribers in 2019

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03965754
United States, Pennsylvania | |
Geisinger | |
Danville, Pennsylvania, United States, 17822 |
Principal Investigator: | Amir Goren, PhD | Geisinger Clinic |
Documents provided by Amir Goren, Geisinger Clinic:
Responsible Party: | Amir Goren, Program Director, Behavioral Insights Team, Geisinger Clinic |
ClinicalTrials.gov Identifier: | NCT03965754 |
Other Study ID Numbers: |
2019-0404 |
First Posted: | May 29, 2019 Key Record Dates |
Results First Posted: | October 5, 2020 |
Last Update Posted: | December 7, 2020 |
Last Verified: | December 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Yes |
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. |
Supporting Materials: |
Study Protocol |
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. |
Access Criteria: | The data on the Open Science Framework will be open to anyone requesting that information. |
URL: | http://osf.io |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Prospect theory |