Exercise-snacks at Work: Impact on Cardiometabolic Parameters
NCT ID: NCT05942144
Last Updated: 2025-04-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
23 participants
INTERVENTIONAL
2023-05-16
2024-07-20
Brief Summary
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Detailed Description
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Aims of this project is therefore to measure the effects of an "exercise-snacks" type physical activity program in the workplace of administrative staff on the cardio-metabolic health and sedentary behaviour of staff.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Exercise-snacks group
They will perform a "exercise-snacks" program and receive information about physical activity
Exercise-snacks program
Subjects in the exercise-snacks group will perform 4 "exercise-snacks" sessions per working day for 4 weeks. These sessions will consist of 80 one-to-one walks to be completed as quickly as possible. They will also receive information about their attitudes to physical activity.
Control group
They will maintain their usual lifestyle until the end of the study
No interventions assigned to this group
Interventions
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Exercise-snacks program
Subjects in the exercise-snacks group will perform 4 "exercise-snacks" sessions per working day for 4 weeks. These sessions will consist of 80 one-to-one walks to be completed as quickly as possible. They will also receive information about their attitudes to physical activity.
Eligibility Criteria
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Inclusion Criteria
* age between 30 and 60,
* body mass index ≥25kg/m²,
* sedentary time ≥7h/day,
* minimum 3 working days on site,
* no known cardiovascular or metabolic pathology, social security affiliation or benefit,
* ability and willingness to give free, written and informed consent.
Exclusion Criteria
* anti-hypertensive treatment, beta-blockers and anti-diabetics,
* known contraindications to physical activity (articular, cardiac or other),
* exercise-induced asthma,
* lack of motivation of subjects posing problems of compliance and adherence to the exercise program,
* participation in a study in the preceding 3 months, ongoing participation in a clinical trial.
30 Years
60 Years
ALL
Yes
Sponsors
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University of Avignon
OTHER
Responsible Party
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Principal Investigators
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Agnès VINET
Role: PRINCIPAL_INVESTIGATOR
Avignon University - LaPEC
Locations
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Avignon University
Avignon, , France
Countries
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Other Identifiers
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AU-062023-AVJ
Identifier Type: -
Identifier Source: org_study_id
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