Sedentary Behavior Clinical Trial
— REMOVEOfficial title:
Effects of Cycling Workstation on Cardiometabolic Health for Workers With an Office-sitting Desk
The recent literature has highlighting the importance of the time of inactivity and the level
of physical activity (PA) as predictors of metabolic cardio risks. Now, sedentary lifestyles
are well recognized as one of the causes of mortality. As with physical activity, a
dose-response relationship appears to exist: mortality would increase with time spent in
sedentary behaviors. However, this relationship would not be linear: the more the daily
sitting time increases, the more the consequences on mortality are important. It is now well
demonstrated that time spent in sedentary adult behaviour finds primarily its origin in the
work, characterized by prolonged and uninterrupted periods of sitting. Many strategies have
been settled to break the prolonged sitting time. The most promising one seem to be the use
of active workstations (treadmill, cycling, stepping) because they reduce sedentary time at
work and increase physical activity with positive effects on the global health. If active
workstations have demonstrated their effectiveness with overweight or obese people by
increasing daily energy expenditure, their interest in prevention in normal weight people is
less known. In addition, the long-term effectiveness of a program of reactivation by active
workstation on biological parameters, quantitative and qualitative time of sedentary
behaviour (duration, number of breaks) and physical fitness was not assessed.
The main objective of this project is to study the effects of the use of a cycling
workstation for 60 minutes per day (30 minutes twice a day) for 3 months among professionals
with an office-sitting desk on overall quantity of physical activity time (work and non-work)
and sedentary time.
Status | Recruiting |
Enrollment | 75 |
Est. completion date | January 2022 |
Est. primary completion date | January 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 61 Years |
Eligibility |
Inclusion Criteria: - Healthy volunteer, male or female, between 18 and 61 years old - Body mass index > 18,5 kg/m2 and = 35 kg/m2 - More than 0.8 full time equivalent hours (FTE) with 75% of this time in a sitting position - Able to provide informed consent to research participation - Registered in the French social security system Exclusion Criteria: - Work involving multiple periods of sitting interruptions >1 minute - Subject using a sit-to-stand office desk or a swiss ball - Sports activity > 2.5 hours/week - Contact jobs (face-to-face with people) - Pregnant or breastfeeding women - Medical or surgical history determined by principal investigator to be not compatible with the study - Subject with cardiorespiratory and/or osteo-articular disorders limiting their ability to perform physical tests or the use of active offices - Subject with type 1 or type 2 diabetes treated with insulin - Subject with progressive cardiovascular or neoplastic disease. - Subject with a major infection within 3 months of inclusion. - Subject with known neuromuscular pathology: myopathy, myasthenia, rhabdomyolysis, paraplegia, hemiplegia - Subject with chronic or acute inflammatory pathology 3 months prior to inclusion - Subject treated by beta-blocker - Subject diagnosed and/or treated for schizophrenia, bipolar disorders, major depression - Subject treated, or having stopped treatment for less than 3 months prior to inclusion, by corticosteroids, immunosuppressant, anabolic, growth hormone. - Subject with unstable psychiatric condition - Significant alcohol consumption (> 2-3 drinks per day depending on gender) or presence of substance abuse. - Unable to walk or pedal 45 minutes in a row - Subject who is excluded from another study or who received more than €4,500 in the year following his participation in clinical studies - Subject deprived of their liberty by judicial or administrative decision - Refusal to sign written consent to participate - Subject participating in another study |
Country | Name | City | State |
---|---|---|---|
France | CHU de Clermont-Ferrand | Clermont-Ferrand |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Clermont-Ferrand | Laboratoire AME2P - Unversité Clermont Auvergne |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | effects of the use of a cycling Workstation for 60 minutes per day (30 minutes twice a day) for 3 months among professionals with an office-sitting desk on overall quantity of physical activity time (work and non-work) and sedentary time | Quantify by the use of an accelerometer device wears at the hip | month 3 | |
Secondary | Body composition | Body fat mass, body fat free mass will be assessed by bioimpedance analysis | day 90 | |
Secondary | Body composition | Body fat mass, body fat free mass will be assessed by bioimpedance analysis | day 180 | |
Secondary | Body composition | Body fat mass, body fat free mass will be assessed by bioimpedance analysis | day 1 | |
Secondary | Biological parameters - insulin | will be assessed in the fasting state using blood sample (insulin mlUI/L) | Day 1 | |
Secondary | Biological parameters - insulin | will be assessed in the fasting state using blood sample (insulin mlUI/L) | Day 90 | |
Secondary | Biological parameters - insulin | will be assessed in the fasting state using blood sample (insulin mlUI/L) | Day 180 | |
Secondary | Biological parameters - glucose | will be assessed in the fasting state using blood sample (glucose g/L) | Day 1 | |
Secondary | Biological parameters - glucose | will be assessed in the fasting state using blood sample (glucose g/L) | Day 90 | |
Secondary | Biological parameters - glucose | will be assessed in the fasting state using blood sample (glucose g/L) | Day 180 | |
Secondary | Biological parameters - triglycerides | will be assessed in the fasting state using blood sample (triglycerides g/L) | Day 1 | |
Secondary | Biological parameters - triglycerides | will be assessed in the fasting state using blood sample (triglycerides g/L) | Day 90 | |
Secondary | Biological parameters - triglycerides | will be assessed in the fasting state using blood sample (triglycerides g/L) | Day 180 | |
Secondary | Biological parameters - cholesterol | will be assessed in the fasting state using blood sample (cholesterol g/L) | Day 1 | |
Secondary | Biological parameters - cholesterol | will be assessed in the fasting state using blood sample (cholesterol g/L) | Day 90 | |
Secondary | Biological parameters - cholesterol | will be assessed in the fasting state using blood sample (cholesterol g/L) | Day 180 | |
Secondary | Biological parameters - CRP | will be assessed in the fasting state using blood sample (CRP-us mg/L) | Day 1 | |
Secondary | Biological parameters - CRP | will be assessed in the fasting state using blood sample (CRP-us mg/L) | Day 90 | |
Secondary | Biological parameters - CRP | will be assessed in the fasting state using blood sample (CRP-us mg/L) | Day 180 | |
Secondary | Biological parameters - anandamide | will be assessed in the fasting state using blood sample (plasma concentration anandamide pmol/ml) | Day 1 | |
Secondary | Biological parameters - anandamide | will be assessed in the fasting state using blood sample (plasma concentration anandamide pmol/ml) | Day 90 | |
Secondary | Biological parameters - anandamide | will be assessed in the fasting state using blood sample (plasma concentration anandamide pmol/ml) | Day 180 | |
Secondary | Psychological assessment | Through an evaluation of healthy life span, stress at work and outside, stress management and anxiety (questionnaires) | Day 1 | |
Secondary | Psychological assessment | Through an evaluation of healthy life span, stress at work and outside, stress management and anxiety (questionnaires) | Day 90 | |
Secondary | Psychological assessment | Through an evaluation of healthy life span, stress at work and outside, stress management and anxiety (questionnaires) | Day 180 | |
Secondary | Resting metabolic rate | will be assessed at rest during 30 minutes using indirect calorimetry | Day 1 | |
Secondary | Resting metabolic rate | will be assessed at rest during 30 minutes using indirect calorimetry | Day 90 | |
Secondary | Resting metabolic rate | will be assessed at rest during 30 minutes using indirect calorimetry | Day 180 | |
Secondary | Physical capacity | will be assessed with the Step Test 6 minutes | Day 1 | |
Secondary | Physical capacity | will be assessed with the Step Test 6 minutes | Day 90 | |
Secondary | Physical capacity | will be assessed with the Step Test 6 minutes | Day 180 | |
Secondary | Muscle Strength | will be assessed with handgrip for upper limb muscle and isokinetic dynamometer for lower limb muscle | Day 1 | |
Secondary | Muscle Strength | will be assessed with handgrip for upper limb muscle and isokinetic dynamometer for lower limb muscle | Day 90 | |
Secondary | Muscle Strength | will be assessed with handgrip for upper limb muscle and isokinetic dynamometer for lower limb muscle | Day 180 | |
Secondary | Quality of the time spend to physical activities and sedentary behaviour | moderate and high intensity physical activity low intensity physical activity total sedentary time number of sedentary periods of =30 minutes, =10 minutes, 10 to 30 minutes Evaluate by the use of an accelerometer device wears at the hip |
Day 1 | |
Secondary | Quality of the time spend to physical activities and sedentary behaviour | moderate and high intensity physical activity low intensity physical activity total sedentary time number of sedentary periods of =30 minutes, =10 minutes, 10 to 30 minutes Evaluate by the use of an accelerometer device wears at the hip |
Day 90 | |
Secondary | Quality of the time spend to physical activities and sedentary behaviour | moderate and high intensity physical activity low intensity physical activity total sedentary time number of sedentary periods of =30 minutes, =10 minutes, 10 to 30 minutes Evaluate by the use of an accelerometer device wears at the hip |
Day 180 |
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