- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04082624
Workplace Wellness: Improving Your Experience at Work
The primary objective of study was to compare affective (i.e., highlighted emotional benefits), instrumental (i.e., highlighted other health benefits), and self-regulation (i.e., demonstrated ways to plan, set goals, etc.) interventions in terms of their ability to motivate less sitting in the workplace. Research of this type is important because people sit for long periods of time at work which adversely affects their health and productivity.
It was hypothesized that the affective and self-regulation groups would sit less than the instrumental and control groups based on evidence indicating that affective attitude (i.e., emotional evaluation of the behavior) and self-regulation techniques tend to predict behavior.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
British Columbia
-
Victoria, British Columbia, Canada, V8P 5C2
- Behavioural Medicine Laboratory
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- From a local workplace in Victoria
- Full-time employee (i.e., greater than 35 hours per week)
- Reported over 5.5 hours of sitting per day at work
- Agreed to attend the 3 intervention sessions
Exclusion Criteria:
- Not from a local workplace in Victoria
- Not a full-time employee (i.e., 35 hours or less per week)
- Reported less than 5.5 hours of sitting per day at work
- Did not agree to attend the 3 intervention sessions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Nutrition condition
Received nutrition information such as the comparison of nutritional information between orange juice and soda pop.
Received intervention following measurements at baseline, week 4, and week 8.
|
Received nutritional information in in-person PowerPoint presentations.
|
Experimental: Affective condition
Learned about the affective benefits (e.g., less depression) of reduced office sitting time through taking active breaks.
Received intervention following measurements at baseline, week 4, and week 8.
|
Received information about affective benefits of less sitting in the workplace in in-person PowerPoint presentations.
|
Experimental: Instrumental condition
Learned about instrumental benefits such as the relationship between sitting and cardiovascular disease and absenteeism at work.
Received intervention following measurements at baseline, week 4, and week 8.
|
Received information about instrumental benefits of less sitting in the workplace in in-person PowerPoint presentations.
|
Experimental: Self-regulation condition
Learned how to self-monitor their sedentary behavior and active breaks.
They also learned how to create prompts/cues (e.g., sticky note reminder), problem solve to overcome barriers, action plan (i.e., specifying when, where, and how to do the behavior), and set goals in order to be less sedentary according to SMART (i.e., specific, measurable, attainable, relevant, time-oriented) principles.
Received intervention following measurements at baseline, week 4, and week 8.
|
Learned how to self-regulate behavior to sit less in the workplace in in-person PowerPoint presentations.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sitting time
Time Frame: Twelve weeks post-baseline
|
Average hours of sitting time per day at work
|
Twelve weeks post-baseline
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 13-108
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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