Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Sedentary Behavior
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 61 years
Gender
Both males and females

Description

Subject will have a pre-inclusion visit during a medical consultation where the eligibility criteria to participate to this study will be checked. After the inclusion of subject and their agreements to participate to the study, they will know in which group they are : Group who performs 30minutes tw...

Subject will have a pre-inclusion visit during a medical consultation where the eligibility criteria to participate to this study will be checked. After the inclusion of subject and their agreements to participate to the study, they will know in which group they are : Group who performs 30minutes twice a working day from day 1 to day 180 (interventional) Group who performs 30minutes twice a working day from day 90 to day 180 (control) They will have evaluation at three different times : T0 (Day 1), T1 (Day 90), T2 (Day 180). The evaluation will evaluate : overall quantity and quality of physical activity time (work and non-work) and sedentary time Body composition Biological parameters Physical fitness Psychological parameters At the end of the protocol, there will be an assessment of the obstacles or motivations to this program.

Tracking Information

NCT #
NCT04153214
Collaborators
Laboratoire AME2P - Unversité Clermont Auvergne
Investigators
Principal Investigator: Martine Duclos CHU de Clermont-Ferrand