- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07220044
- Original Trial
Effects of Streak-Based Versus Tally-Based Feedback on Daily Lesson Completion During a 30-Day Digital Health Challenge (Streaks)
February 2, 2026 updated by: University of Pennsylvania
The study will test two interventions for increasing engagement with a target behavior, delivered via a digital web application that participants can access using their phones or computers.
For example, in the streak group, users would see how many consecutive days they have completed daily lessons and will be encouraged to extend their streak.
In the tally group, participants will see how many cumulative days they have completed daily lessons and will be encouraged to extend their tally.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The objective of this study is to determine whether tracking people's streak of behavior increases their engagement in that behavior.
To test this, the investigators are designing a web application that participants can access daily using their phones or computers.
Our previous work suggests that streaks may be useful in motivating people to be more productive.
In this study, the investigators change how the investigators operationalize streaks and test streaks in a field context.
Because most previous streak research is on how others perceive someone who has a streak, this work is novel because it examines how encouraging someone to achieve and keep a streak affects behavior in a field context.
The study will test two interventions for increasing engagement with a target behavior, delivered via a digital web application that participants can access using their phones or computers.
For example, in the streak group, users would see how many consecutive days they have completed daily lessons and will be encouraged to extend their streak.
In the tally group, participants will see how many cumulative days they have completed daily lessons and will be encouraged to extend their tally.
The investigators are interested in whether people complete more daily lessons when a 30-day health challenge app provides daily feedback on their consecutive lessons (each comprising two multiple-choice questions) completed (i.e., "streaks") vs. when it provides feedback on their cumulative lessons completed (i.e., "tallies").
Study Type
Interventional
Enrollment (Actual)
7004
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Our target population is 18 and older adults in the United States who have a valid U.S. phone number and who are willing to make an account on our web application for use during the duration of the study.
Exclusion Criteria:
- Children under 18 years of age and adults without a valid U.S. phone number
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: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Tally
In the tally group, participants will see how many cumulative days they have completed daily lessons and will be encouraged to extend their tally.
|
The study will test two interventions for increasing engagement with a target behavior, delivered via a digital web application that participants can access using their phones or computers.
For example, in the streak group, participants would see how many consecutive days they have completed daily lessons and will be encouraged to extend their streak.
In the tally group, participants will see how many cumulative days they have completed daily lessons and will be encouraged to extend their tally.
The investigators are interested in whether people complete more daily lessons when a 30-day health challenge app provides daily feedback on their consecutive lessons (each comprising two multiple-choice questions) completed (i.e., "streaks") vs. when it provides feedback on their cumulative lessons completed (i.e., "tallies").
|
|
Experimental: Streaks
In the streak group, participants would see how many consecutive days they have completed daily lessons and will be encouraged to extend their streak
|
The study will test two interventions for increasing engagement with a target behavior, delivered via a digital web application that participants can access using their phones or computers.
For example, in the streak group, participants would see how many consecutive days they have completed daily lessons and will be encouraged to extend their streak.
In the tally group, participants will see how many cumulative days they have completed daily lessons and will be encouraged to extend their tally.
The investigators are interested in whether people complete more daily lessons when a 30-day health challenge app provides daily feedback on their consecutive lessons (each comprising two multiple-choice questions) completed (i.e., "streaks") vs. when it provides feedback on their cumulative lessons completed (i.e., "tallies").
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Total number of lessons completed
Time Frame: 30 days
|
The key dependent variable is a person's total number of lessons completed during the 30-day Health Daily program.
Participants can only complete a given day's lesson on that day; a lesson is only considered complete if both questions that comprise the lesson are answered.
|
30 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
September 23, 2025
Primary Completion (Actual)
January 21, 2026
Study Completion (Actual)
January 21, 2026
Study Registration Dates
First Submitted
October 21, 2025
First Submitted That Met QC Criteria
October 21, 2025
First Posted (Actual)
October 23, 2025
Study Record Updates
Last Update Posted (Actual)
February 3, 2026
Last Update Submitted That Met QC Criteria
February 2, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DBSR-11288
- P30AG034546-16 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
- Unique ID
- Condition assignment
- Response for the first quiz question for each day
- Response for the second quiz question for each day
- Date
- Female indicator (taken from generize.io)
- Correct response for the first quiz question
- Correct response for the second quiz question
IPD Sharing Time Frame
Individual participant data and all supporting materials will become available upon publication of the primary study manuscript and will remain accessible indefinitely thereafter.
IPD Sharing Access Criteria
Individual participant data and all supporting materials will be made openly available through the Open Science Framework (OSF) to any interested party without access restrictions.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- 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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