- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01410812
Tying Devices as a Means of Increasing Exercise
December 17, 2018 updated by: University of Pennsylvania
The investigators propose that healthy behaviors such as exercise could be increased through the use of tying devices - mechanisms that force a coupling of addictive activities (listening to the next chapter of a page-turner novel) with engagement in a healthy behavior (exercise).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study will test the effect of the following treatments as a means of increasing gym attendance over 10 weeks: 1. Participants receive access to 4 iTunes audio novels on their own iPods and prompted to listen to those novels only when exercising at the gym; 2: Participants receive 4 iTunes audio novels for a loaned iPod that they will only have access to at the gym; 3: Participants receive weekly emails asking them about their exercise.
Study Type
Interventional
Enrollment (Actual)
226
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 to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Stable health as determined by the screening of their medical history
- Own an iPod
- An interest in exercising more regularly
- Belong to the Pottruck Gym at University of Pennsylvania
- Interested in exercising more through the use of aerobic exercise machines
Exclusion Criteria:
- Recent myocardial infraction
- congestive heart failure
- uncontrolled hypertension
- self-report of 6 or more alcoholic beverages per day or use of any illicit drugs
- bulimia nervosa or related behaviors
- diabetes medication
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: Suggested Tying
Receive same treatments as control group, but instead of receiving cash they receive 4 iTunes audio novels for their own iPods.
Further, they are prompted to try to listen to those novels only when exercising at the gym in order to increase their attendance.
|
Participants receive 4 iTunes audio novels for their own iPods to listen to only at the gym
|
|
Experimental: Forced Tying
Receives same treatment as the control group.
However, in addition to receiving the cash, they also receive 4 iTunes audio novels for a loaned iPod that they will only have access to at the gym.
They are told they may only listen to these novels only when at the gym in order to increase their attendance.
|
Participants receive cash and also 4 iTunes audio novels for a loaned iPod accessible only at the gym to listen to only at the gym.
|
|
Experimental: Control
Control group of participants who do not receive any intervention but are weighed at the beginning and end of a 10 week period and receive weekly emails asking them about their exercise.
They also receive the equivalent cash value of 4 iTunes audio novels
|
Receive weekly emails asking participants about their exercise and receive cash.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Average Weekly Gym Attendance From Baseline to Week 9
Time Frame: 9 weeks
|
9 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dollar Amount Participants Would Pay for Enrollment
Time Frame: 9 weeks
|
Willingness to pay is measured as the dollar amount a participant would pay to be enrolled in a program such as the treatment.
Participant who would pay more are said to be more willing to pay, as opposed to those who would pay less or not at all.
|
9 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Katherine L. Milkman, Ph.D., University of Pennsylvania
- Principal Investigator: Julia A Minson, University of Pennsylvania
- Principal Investigator: Kevin G.M. Volpp, MD, 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
September 1, 2011
Primary Completion (Actual)
December 1, 2011
Study Completion (Actual)
September 1, 2012
Study Registration Dates
First Submitted
August 3, 2011
First Submitted That Met QC Criteria
August 4, 2011
First Posted (Estimate)
August 5, 2011
Study Record Updates
Last Update Posted (Actual)
December 19, 2018
Last Update Submitted That Met QC Criteria
December 17, 2018
Last Verified
January 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 813970
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.