- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02933385
Active Your Health: A Workplace Healthy Lifestyle Program
Activate Your Health Program : A Workplace Healthy Lifestyle Program
Study Overview
Status
Detailed Description
Currently, lifestyle habits of workers does not only represents a personal concern, but also a concern of the company. Currently there are very few studies that efficiently integrate classical interventions (screening) and online tools in order to obtain sustainable lifestyle changes in workers. The current project aims to evaluate efficacy of a combined approach versus more traditional approaches. Health Data collected by CAPSANA in the workplace between 2012 and 2014 showed that, out of 4231 workers, 69% should aim at a more active lifestyle and 74% at a better nutritional profile. In addition, 53% of the sampled population were overweight.
In this context, the current project aims to motivate and follow individuals towards a healthier lifestyle. To do so, the Activate Your Health will be implemented and tested using various options (limited to more complete) in several companies. It is planned to compare to a control group receiving no intervention to the other groups containing little to complete set of interventions. The content of the interventions involves health assessment, electronic tools (SOScuisine and social media platform), health screening, activity monitor tool and closing events. The companies had to pick which option they would like to provide their employees. It is anticipated that the complete option will yield better results for the activity profile and other lifestyle habits. For example, changes in eating habits toward better habits are expected.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- French Speaking, work in the participating company.
Exclusion Criteria:
- pregnant women.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: TRIPLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Full lifestyle program
Participants receive all the intervention tools that aimed to enhance lifestyle profile.
|
Home made questionnaire questioning about the participant's lifestyle habits, risk factors and other.
Create interactions between the employees.
Site that is personalized to the employee.
It provides menus, grocery shopping list and other.
Screen for diabetes, cholesterol, blood pressure and body weight.
these aim to motivate the employees to continue into the program.
The first year participant will be coached by a nurse, second year by a nutritionist, and third year by a kinesiologist.
Social Health Platform: employees can challenge themselves or each other.
|
Experimental: High lifestyle program
Participants receive most of the intervention tools that aimed to enhance lifestyle profile.
|
Home made questionnaire questioning about the participant's lifestyle habits, risk factors and other.
Create interactions between the employees.
Site that is personalized to the employee.
It provides menus, grocery shopping list and other.
Screen for diabetes, cholesterol, blood pressure and body weight.
these aim to motivate the employees to continue into the program.
The first year participant will be coached by a nurse, second year by a nutritionist, and third year by a kinesiologist.
|
Experimental: Moderate lifestyle program
Participants receive some intervention tools that aimed to enhance lifestyle profile.
|
Home made questionnaire questioning about the participant's lifestyle habits, risk factors and other.
Create interactions between the employees.
Site that is personalized to the employee.
It provides menus, grocery shopping list and other.
these aim to motivate the employees to continue into the program.
The first year participant will be coached by a nurse, second year by a nutritionist, and third year by a kinesiologist.
|
Experimental: Light lifestyle program
Participants receive little intervention tools that aimed to enhance lifestyle profile.
|
Home made questionnaire questioning about the participant's lifestyle habits, risk factors and other.
Create interactions between the employees.
Site that is personalized to the employee.
It provides menus, grocery shopping list and other.
|
No Intervention: Control group
Participants receive none of the intervention tools that aimed to enhance lifestyle profile.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Physical activity profile (intensity, frequency and duration) measured by questionnaire
Time Frame: 365 days
|
Based on a questionnaire we will be able to calculate physical activity duration, intensity and frequency will be obtained.
|
365 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Nutritional profile (fruit and vegetables intake) will be obtained by questionnaire
Time Frame: 365 days
|
Based on a questionnaire we will be able to calculate nutrition parameters (# of fruits and vegetables per day).
|
365 days
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
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
- University of Montreal
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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