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

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.

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

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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