- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03742765
Incentivizing Planning & Output in Exercising
June 9, 2020 updated by: University of Pennsylvania
This study will test whether incentivizing pre-workout activities (i.e., planning workouts) is more effective than incentivizing actual workouts.
This study has two conditions: planning condition (with incentives for planning) vs. output (with incentives for working out).
The focus of the incentives will be reinforced by three text messages per week and weekly emails.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Gym members register online to participate in a 28-day workout program.
Upon registration, participants are assigned to one of two conditions (a condition that incentivizes planning or a condition that incentivizes workouts).
Upon registration, participants are prompted to create a workout schedule and are given tips about how to create a workout habit.
Over the 28-day intervention period, participants receive text message reminders prior to their scheduled workouts and emails reminding them of their schedules.
In both conditions, participants receive points every day that they go to the gym, which can be redeemed for a gift card after the intervention period.
In the planning condition, participants can receive bonus points for responding to each of three text messages each week asking about their plans for going to the gym.
In the output condition, participants receive bonus points for their first three workouts each week.
Study Type
Interventional
Enrollment (Actual)
1200
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
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Has 24 Hour Fitness gym membership
Exclusion Criteria:
-
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Incentivizing Planning
Participants will receive three texts each week asking a question to help plan for the next workout, and will receive 500 points for each text they answer.
These bonus points are on top of points participants receive for each workout (200 points per workout).
|
Participants receive bonus incentives for planning their workouts
|
Experimental: Incentivizing Exercise
Participants will receive three texts each week asking a question about their workout.
Regardless of whether or not they respond to the texts, participants receive 500 bonus points for their first three workouts during the week.
These bonus points are on top of points participants receive for each workout (200 points per workout).
|
Participants receive bonus incentives for exercising
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Gym visits per week
Time Frame: During the 28-day intervention period
|
Number of times the participant goes to the gym
|
During the 28-day intervention period
|
Gym visits per week
Time Frame: During the 4-weeks post-intervention
|
Number of times the participant goes to the gym
|
During the 4-weeks post-intervention
|
Gym visits per week
Time Frame: During the 10-weeks post-intervention
|
Number of times the participant goes to the gym
|
During the 10-weeks post-intervention
|
Whether or not a participant visits the gym in a given week
Time Frame: During the 28-day intervention period
|
Binary variable capturing whether or not a participant had any gym visits in a given week
|
During the 28-day intervention period
|
Whether or not a participant visits the gym in a given week
Time Frame: During the 4-weeks post intervention
|
Binary variable capturing whether or not a participant had any gym visits in a given week
|
During the 4-weeks post intervention
|
Whether or not a participant visits the gym in a given week
Time Frame: During the 10-weeks post intervention
|
Binary variable capturing whether or not a participant had any gym visits in a given week
|
During the 10-weeks post intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Gym visits per week
Time Frame: During the 52-weeks post-intervention
|
Number of times the participant goes to the gym
|
During the 52-weeks post-intervention
|
Whether or not a participant visits the gym in a given week
Time Frame: During the 52-weeks post-intervention
|
Binary variable capturing whether or not a participant had any gym visits in a given week
|
During the 52-weeks post-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)
January 31, 2018
Primary Completion (Actual)
February 28, 2019
Study Completion (Actual)
February 28, 2019
Study Registration Dates
First Submitted
November 13, 2018
First Submitted That Met QC Criteria
November 13, 2018
First Posted (Actual)
November 15, 2018
Study Record Updates
Last Update Posted (Actual)
June 11, 2020
Last Update Submitted That Met QC Criteria
June 9, 2020
Last Verified
June 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 827107-1255
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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