- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01811407
Impacts of Public Announcements of Goals and Outcomes on Goal Completion (Commit to Steps)
Impacts of Public Announcements of Goals and Outcomes on Goal Completion
Physical activity is known to help reduce obesity and the problems that accompany it. Walking has many benefits that make it an excellent way for obese people to increase their physical activity. It is hard, however, for people to stick with walking programs. Setting specific and challenging walking targets that are combined with timely feedback about discrepancies between desired and actual performance lead to higher performance. There is conflicting theory and evidence about the effects of publicly announcing those targets on commitment to the targets and on performance.
Our research question is whether public announcements reduce the challenge level of commitments people set, and whether the reputational consequence of public announcements is severe enough to increase performance. The investigators propose a controlled trial that will integrate Facebook with the objective monitoring of walking via the use of pedometers to test the effect of public announcements on commitments and step counts.
All participants will wear a pedometer and upload via the internet for 14 to 15 weeks, depending on their date of randomization. The first 2 to 3 weeks the investigators will determine the participant's baseline step counts. The following 12 weeks, the investigators will recommend a daily step count target based on the median number of steps the participants walked the previous week. Each week, participants will set a commitment by stating the number of days in the following week that he/she will meet the computer-set step count target.
Commitments will be entered into an interface that will link with Facebook. Participants will select who of their Facebook friends will receive their commitments and/or results via Facebook posts. The interface will distribute those posts in a way that fits in with existing online social practices.
There will be 3 experimental conditions. 1.) No public announcements 2.) Public announcement of commitment and 3.) Public announcement of commitment and results. In addition, groups 2 and 3 will provide us with emails of 3 friends or family members who will act as the participant's support team. The investigators will send announcements directly to support team members.
The investigators plan to recruit 165 participants primarily by obtaining lists of potentially eligible University of Michigan Health System patients from the clinical data repository, and sending targeted letters to these patients. Because this research - and the physical activity programs it will inform - aims to reach a large number of people efficiently, enrollment will take place online with a click-through consent document. The investigators have extensive experience with delivering online walking programs in similar populations.
The investigators hope to learn best practices for using public announcements and online social networks to encourage people to exercise more or to otherwise promote wellness.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Michigan
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Ann Arbor, Michigan, United States, 48109
- University of Michigan
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria
- Has received treatment from a UMHS provider within the previous 6 months.
- BMI ≥ 30
- Age ≥ 18
- Must be sedentary, defined by less than 150 minutes of self-reported activity per week.
- Must have access to a computer with an Internet connection that can accept USB uploads.
- Must have a Facebook account and have at least 50 friends on it.
- Must be able to communicate in English.
Exclusion Criteria
- Currently pregnant
- Unable to comfortably walk at least a block without the assistance of a cane or walker.
- Not competent to sign a consent form.
- Absolute or relative contraindications to walking
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Private/private
Participants will wear a pedometer for 14-15 weeks and receive a weekly step count target each week.
Participants will be required to set a forward-looking commitment each week as to how many days during the following week they will meet their step count target.
Commitment and results will be private.
|
|
|
Experimental: Public/private
Participants will wear a pedometer for 14-15 weeks and receive a weekly step count target each week.
Commitments are made as in the Private/Private condition.
In addition, one Facebook announcement will be posted at the beginning of the week that says how many days the participant thinks they will meet their walking target the following week.
An email will also be sent directly to 3 friends the participant chose with the same announcements.
|
|
|
Experimental: Public/public
Participants will wear a pedometer for 14-15 weeks and receive a weekly step count target each week.
Commitments will be made as in the Private/Private condition.
In addition, one message will be posted to Facebook at the beginning of the week that says how many days the participant thinks they will meet their walking target the following week, and how they did on their previous weekly commitment.
An email will also be sent directly to 3 friends the participant chose with the same announcements.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The number of days the participant met the weekly step count target.
Time Frame: Participants will be followed for 14 to 15 weeks, depending on the date of randomization.
|
Participants will be followed for 14 to 15 weeks, depending on the date of randomization.
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The number of days the participants committed to walking.
Time Frame: Participants will be followed for 14 to 15 weeks, depending on the date of randomization.
|
Participants will be followed for 14 to 15 weeks, depending on the date of randomization.
|
|
The change in step counts from baseline.
Time Frame: Participants will be followed for 14 to 15 weeks, depending on the date of randomization.
|
Participants will be followed for 14 to 15 weeks, depending on the date of randomization.
|
|
The number of days the participants wore the pedometer.
Time Frame: Participants will be followed for 14 to 15 weeks, depending on the date of randomization.
|
Participants will be followed for 14 to 15 weeks, depending on the date of randomization.
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Paul J Resnick, PhD, University of Michigan
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 9010
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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