- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03649893
Effectivness of Active Office Intervention (ActiveOffice)
October 1, 2019 updated by: Nejc Sarabon, University of Primorska
The Effectivness of Multi-modal Intervention for Reducing Sedentary Behavior in Office Workers
The Active Office study is focusing on interventions with potential to reduce sedentary behavior and increase physical activity in office workers.
The participants will be devided in two groups, the experimental and the control group.
The participants in the experimental group will use active office (sit-to-stand desk, bike desk, seddle chair and active breaks) for one week, whereas the control group will remain in the conventional sitting-desk office.
All the participants will wear ActivePal for 5 consecutive day and complete the measurements (heart rate, blood pressure).
The goal of the study is to evaluate the effects of active office on sedentary behavior and physical activity levels in office workers.
Study Overview
Detailed Description
Sedentary behavior is racognised as an independent risk factor for the development of non-communicable diseases.
It is estimated that office workers spent up to 80 % of their working time sedentary and do not compensate by sitting less in their leisure time.
Therefore, interventions with potential to reduce sedentary behavior and increase phyical activity levels are of increasing interest.
The aim of this study is to evaluate the effects of active office, including sit-to-stand desk, bike desk, seddle chair, and active breaks, on sedentary behavior, physical activity levels, and cardio-vascular parameters.
The study design will be randomised control trial with one experimental and one control group.
The participants in the experimental group will use active office for one week whereas the control group will use the conventional office.
All the participants will wear ActivePal for 5 consecutive day and complete the measurements (heart rate, blood pressure).
The participants will also complete quastionaires about the sedentary behavior and physical activity levels (Sedentary Behavior Questionnaire, Global Physical Activity Questionnaire).
Moreover, at the baseline and on the last day of measurements the investigators will measure the work environment factors (light, noise, air flow, temperature).
The goal of the study is to evaluate the effects of active office on sedentary behavior and physical activity levels in office workers.
Study Type
Interventional
Enrollment (Anticipated)
20
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
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Izola, Slovenia, 6310
- InnoRenew
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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 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- office workers spending at least 70 % of their working time sedentary
- aged between 18 and 65
Exclusion Criteria:
- body mass index > 30kg/m2
- pain presence in any musculokeletal part > 3 on 10-level scale
- presence of any non-communicable chronical diseases
- pregnancy
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: Device Feasibility
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control Group
The control group will use conventional siiting-desk office.
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Experimental: Active Office Group
The experimental group will use active offfice, including sit-to-stand desk, bike desk, seddle chair and active breask.
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Active Office intervention includes sit-to-stand desk, bike desk, seddle chair, and active breaks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Weekly physical activity levels
Time Frame: 5 days
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Weekly physical activity levels will be measured with ActivePal sensors.
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5 days
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Weekly sitting time
Time Frame: 5 days
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Weekly sitting time will be measured with ActivePal sensors.
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5 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Heart rate
Time Frame: 5 days
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Heart rate will be measured with Polar Heart Rate Monitor.
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5 days
|
Blood Pressure
Time Frame: Baseline and after 5 days
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Blood pressure will be measured with electronic blood pressure monitor.
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Baseline and after 5 days
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Global Physical Activity Questionnaire
Time Frame: Baseline and after 5 days
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Global Physical Activity Questionnaire is used to subjectively assess physical activity levels.
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Baseline and after 5 days
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Sedentary Behavior Questionnaire
Time Frame: Baseline and after 5 days
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Sedentary Behavior Questionnaire is used to subjectively assess sedentary behavior.
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Baseline and after 5 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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 (Anticipated)
December 5, 2019
Primary Completion (Anticipated)
February 1, 2020
Study Completion (Anticipated)
March 1, 2020
Study Registration Dates
First Submitted
August 24, 2018
First Submitted That Met QC Criteria
August 27, 2018
First Posted (Actual)
August 28, 2018
Study Record Updates
Last Update Posted (Actual)
October 2, 2019
Last Update Submitted That Met QC Criteria
October 1, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Active Office
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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