- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01139541
Testing Strategies for Increasing Exercise
The purpose of the study is to learn more about effective ways to motivate people to increase their non-exercise energy expenditure exercise. This is an important research question because obesity and weight-related issues are increasingly becoming a problem in America. This project will address this research question by testing the effect of group dynamics in motivating employees who are predominantly sedentary to use Walkstations at work. The Walkstations are treadmills that move at a very slow rate (maximum 2miles / hour) and are attached to a work station (i.e. with computer and telephone); they therefore are designed to increase energy spent not through heavy exercise, but through small changes in posture and movement associated with routines in daily life (called nonexercise activity thermogenesis or NEAT). The proposed study is designed to build upon previous research (Levine et al., 2005) suggesting the role of NEAT-enhanced behaviors in weight loss.
In this study, the investigators are interested in the impact of group dynamics on the propensity to use the Walkstations. Participants in the active arms will be asked to use the Walkstations for at least 3 hours per week. They will do so by signing up for a time slot. During their session, they will be asked to log into the scheduling system to indicate that they are using the Walkstation. Walkstation usage will be assessed by log-in data: employees will log-in to the phone and computer when they use the Walkstation. This log-in data is work-station specific; therefore the investigators will be able to tell when a given subject used the Walkstation.
Subjects will be randomly assigned to one of three conditions:
- Individual. In the individual condition, participants will not be part of a team. They will receive weekly email feedback on their Walkstation performance (e.g. number of time slots they signed up for, and number of times they showed up for the time slot.) Participants will also receive a wellness tip in each email. (see appendix for a sample email)
- Pairs. In the pair condition, participants will be randomly assigned to a partner. They will receive the same feedback as those in the individual condition, for both themselves AND their partner.
- Group. In the group condition, participants will be randomly assigned to a group of 5 people. They will receive the same feedback as those in the individual condition, for both themselves AND each member of their group.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02215
- Blue Cross Blue Shield Massachusetts
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Must pass the ParQ
- Must be employee of BCBS Massachusetts
Exclusion Criteria:
- Failing the ParQ
- Not being an employee of BCBS Massachusetts
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
Participants in the control condition will be asked to refrain from using the WalkStations during the study period.
|
|
|
Experimental: Individual
In the individual condition, participants will not be part of a team.
They will receive weekly email feedback on their Walkstation performance (e.g.
number of time slots they signed up for, and number of times they showed up for the time slot.)
|
In this intervention, we are interested in the impact of group dynamics on the propensity to use the Walkstations.
The intervention consists of 4 levels: control, individual, pair, and group.
|
|
Experimental: Pairs
In the pair condition, participants will be randomly assigned to a partner.
They will receive the same feedback as those in the individual condition, for both themselves AND their partner.
|
In this intervention, we are interested in the impact of group dynamics on the propensity to use the Walkstations.
The intervention consists of 4 levels: control, individual, pair, and group.
|
|
Experimental: Groups
In the group condition, participants will be randomly assigned to a group of 5 people.
They will receive the same feedback as those in the individual condition, for both themselves AND each member of their group.
|
In this intervention, we are interested in the impact of group dynamics on the propensity to use the Walkstations.
The intervention consists of 4 levels: control, individual, pair, and group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
WalkStation usage
Time Frame: 3 months
|
Frequency with which the participant uses the WalkStation
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Creativity
Time Frame: 3 months
|
Creativity measured on versus off the WalkStation.
|
3 months
|
|
Focus
Time Frame: 3 months
|
Focus, as measured when person is on versus off the WalkStation.
|
3 months
|
|
Health Behaviors Survey
Time Frame: pre-baseline
|
Survey of health-related behaviors to be completed by participant.
|
pre-baseline
|
|
WalkStation Usage
Time Frame: 6 months
|
Frequency with which the participant uses the WalkStation
|
6 months
|
|
Health Behaviors Survey
Time Frame: baseline
|
Survey of health-related behaviors to be completed by participant.
|
baseline
|
|
Health Behaviors Survey
Time Frame: 6 months
|
Survey of health-related behaviors to be completed by participant.
|
6 months
|
|
Creativity
Time Frame: baseline
|
Creativity measured on versus off the WalkStation.
|
baseline
|
|
Focus
Time Frame: baseline
|
Focus, as measured when person is on versus off the WalkStation.
|
baseline
|
Collaborators and Investigators
Sponsor
Collaborators
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
- WalkStation1
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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