Pilot Study of Active Desk in Primary School : Effects on Cognitive Capacities, Physical Capacities and Well-being (BICLASS)

May 25, 2022 updated by: University Hospital, Clermont-Ferrand

Pilot Study of Active Desk in Primary School : Effects on the Attention, Cognitive Capacities, Physical Capacities, Concentration and Well-being of Student and on the Classroom Climate

Physical activity (PA) is insufficient in children with three quarters of them who do not meet the WHO's recommendations. Physical inactivity is growing during adolescence; in part due to the time spend in sedentary behaviors at school. The recent literature is highlighting the importance of physical activity on academic achievement, physical fitness and academic achievement in children. In addition, deleterious effects of sedentary behaviors have been demonstrated. At school, many strategies have been settled to break the prolonged sitting time. The use of workstations is one of them and allows to reduce sedentary time at school and increases physical activity without interrupting class. Active workstations like bike desks have demonstrated their effectiveness on physical activity but their effects have not been evaluated in primary school in France. In addition, few studies have evaluated the effects of bike desk use on the child's cognitive abilities.

The main objective of this project is to measure the variations linked to the use of bike desks (desk with pedals) for an average of 1h45mn per week (30min 3 to 4 times per week) for 13 weeks during school time in primary school pupils (aged 8 to 11 years) on the cognitive abilities (mental flexibility, working memory and inhibition) of children.

Our hypothesis is that the use of the bike desk for 1h45 per week will induce an increase in the attention and cognitive capacities (mental flexibility, working memory and inhibition) of the children. Other improvements that should be identified are the child's body composition, the classroom climate and the well-being of pupils and teachers. The children's physical capacities could also be increased, beyond what is expected given the normal evolution during the year.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Two prospective schools have given their prior agreement : Sevigne Lafaye (Vichy) and Pierre Brossolette (Riom). The use of the bike desks in the classroom is part of the school project and will start at the same time as the study. There are 4 bike-desks in each class: 3 for the children and 1 for the teacher. Students pedaling during an overall of 13 weeks (7 weeks and 6 weeks) separated of one evaluation session week (T1). During weeks with evaluation sessions, children will not use bike desk. All children will therefore use the bike desks but only those who have signed the consent form.

An information meeting will be proposed in each school (visit 1). Then, subjects will have a pre-inclusion visit during a medical consultation where the eligibility criteria to participate in this study will be checked (visit 2). The children who have given their consent will have to participate in different evaluation sessions: baseline (T0), between to two pedaling sessions (T1) and at the end of the second session (T2). They are two parts of assessments for each session (T0, T1, T2):

  • Cognitive test and the physical activity attraction test (visits 3, 5, 7)
  • Body composition and physical capacity assessment (visits 4, 6, 8) Questionnaires will also be part of the assessment (T1 and T2).

Study Type

Interventional

Enrollment (Actual)

75

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

      • Clermont-Ferrand, France
        • CHU Clermont-Ferrand

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

8 years to 11 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Children between 8 and 11 years old (inclusive)
  • Girls and boys
  • Children enrolled in CM1a and CM1b classes at the Pierre Brossolette school in Riom and in CM1/CM2 and CM2 classes at the Sévigné-Lafaye school in Vichy.
  • Able to provide informed consent to research participation
  • Registered in the French social security system

Exclusion Criteria:

  • Medical or surgical history judged by the investigator to be incompatible with the study
  • Any unstabilised chronic pathology
  • Inability to pedal
  • Inability or contraindication to physical activity
  • Subjects with cardiorespiratory and/or osteoarticular disorders that limit their ability to perform physical tests or use the cycle desks
  • Subjects with a progressive cardiovascular or neoplastic disease.
  • Subjects with a major infection in the 3 months prior to inclusion
  • Subject with chronic or acute inflammatory disease in the 3 months prior to inclusion
  • Subject diagnosed and/or treated for schizophrenia, bipolar disorder, major depression
  • Person under guardianship, curatorship or not subject to a social security scheme
  • Refusal to sign written consent to participate by the participant or a parent or guardian

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: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Bike desks in classroom
All participants receive the same intervention: the use of bike desks during school.
Children will use bike desks for 13 weeks during school time

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Students cognitive abilities
Time Frame: Week 0
Time to complete the Trail Making Test part A and B (seconds)
Week 0
Students cognitive abilities
Time Frame: 7 weeks
Time to complete the Trail Making Test part A and B (seconds)
7 weeks
Students cognitive abilities
Time Frame: 13 weeks
Time to complete the Trail Making Test part A and B (seconds)
13 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Weight
Time Frame: Week 0
Weight (kg) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan)
Week 0
Body composition (body mass index)
Time Frame: Week 0
Body mass index (kg/m^2) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan) by combining weight and height
Week 0
Body composition (body fat mass)
Time Frame: Week 0
Body fat mass (%) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan)
Week 0
Weight
Time Frame: 7 weeks
Weight (kg) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan)
7 weeks
Body composition (body mass index)
Time Frame: 7 weeks
Body mass index (kg/m^2) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan) by combining weight and height
7 weeks
Body composition (body fat mass)
Time Frame: 7 weeks
Body fat mass (%) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan)
7 weeks
Weight
Time Frame: 13 weeks
Weight (kg) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan)
13 weeks
Body composition (body mass index)
Time Frame: 13 weeks
Body mass index (kg/m^2) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan) by combining weight and height
13 weeks
Body composition (body fat mass)
Time Frame: 13 weeks
Body fat mass (%) will be assessed by bioimpedance analysis with Tanita MC-780 (Tanita Corp., Tokyo, Japan)
13 weeks
Physical fitness (cardio-respiratory capacity)
Time Frame: Week 0
Cardio-respiratory capacity will be assessed with 20 m shuttle test (ml.mn.kg-1)
Week 0
Physical fitness (cardio-respiratory capacity)
Time Frame: 7 weeks
Cardio-respiratory capacity will be assessed with 20 m shuttle test (ml.mn.kg-1)
7 weeks
Physical fitness (cardio-respiratory capacity)
Time Frame: 13 weeks
Cardio-respiratory capacity will be assessed with 20 m shuttle test (ml.mn.kg-1)
13 weeks
Physical fitness (muscular strength)
Time Frame: Week 0
Muscular strength will be assessed with Standing Broad Jump test (cm), Countermovement Jump test (cm) and Throw Medicine Ball test (cm)
Week 0
Physical fitness (upper limbs muscular strength)
Time Frame: Week 0
Muscular strength will be assessed with Handgrip test (kg)
Week 0
Physical fitness (muscular strength)
Time Frame: 7 weeks
Muscular strength will be assessed with Standing Broad Jump test (cm), Countermovement Jump test (cm) and Throw Medicine Ball test (cm)
7 weeks
Physical fitness (upper limbs muscular strength)
Time Frame: 7 weeks
Muscular strength will be assessed with Handgrip test (kg)
7 weeks
Physical fitness (muscular strength)
Time Frame: 13 weeks
Muscular strength will be assessed with Standing Broad Jump test (cm), Countermovement Jump test (cm) and Throw Medicine Ball test (cm)
13 weeks
Physical fitness (upper limbs muscular strength)
Time Frame: 13 weeks
Muscular strength will be assessed with Handgrip test (kg)
13 weeks
Physical fitness (motor skills)
Time Frame: Week 0
Motor skills will be assessed with the time to complete an obstacle course (seconds)
Week 0
Physical fitness (motor skills)
Time Frame: 7 weeks
Motor skills will be assessed with the time to complete an obstacle course (seconds)
7 weeks
Physical fitness (motor skills)
Time Frame: 13 weeks
Motor skills will be assessed with the time to complete an obstacle course (seconds)
13 weeks
Implicit and explicit attraction to physical activity
Time Frame: Week 0
Implicit and explicit attraction to physical activity will be assessed with Activity Preference Assessment (APA) computer test
Week 0
Implicit and explicit attraction to physical activity
Time Frame: 7 weeks
Implicit and explicit attraction to physical activity will be assessed with Activity Preference Assessment (APA) computer test
7 weeks
Implicit and explicit attraction to physical activity
Time Frame: 13 weeks
Implicit and explicit attraction to physical activity will be assessed with Activity Preference Assessment (APA) computer test
13 weeks
Teachers' perceptions of students' well-being
Time Frame: Week 0
Questionnaire created by the National Education. Items will be rated from 1 to 5: 1 unsatisfactory; 2 marginally satisfactory; 3 neutral; 4 satisfactory; 5 very satisfactory. Higher scores mean a better outcome.
Week 0
Teachers' perceptions of students' well-being
Time Frame: 7 weeks
Questionnaire created by the National Education. Items will be rated from 1 to 5: 1 unsatisfactory; 2 marginally satisfactory; 3 neutral; 4 satisfactory; 5 very satisfactory. Higher scores mean a better outcome.
7 weeks
Teachers' perceptions of students' well-being
Time Frame: 13 weeks
Questionnaire created by the National Education. Items will be rated from 1 to 5: 1 unsatisfactory; 2 marginally satisfactory; 3 neutral; 4 satisfactory; 5 very satisfactory. Higher scores mean a better outcome.
13 weeks
Students and teachers' perceived well-being
Time Frame: 7 weeks
Questionnaire created by the National Education. Items will be rated with smiley or rating from 1 to 5: 1 unsatisfactory; 2 marginally satisfactory; 3 neutral; 4 satisfactory; 5 very satisfactory. Higher scores mean a better outcome.
7 weeks
Students and teachers' perceived well-being
Time Frame: 13 weeks
Questionnaire created by the National Education. Items will be rated with smiley or rating from 1 to 5: 1 unsatisfactory; 2 marginally satisfactory; 3 neutral; 4 satisfactory; 5 very satisfactory. Higher scores mean a better outcome.
13 weeks
Classroom climate/atmosphere
Time Frame: 7 weeks
Questionnaire created by the National Education. Items will be rated from 1 to 5: 1 unsatisfactory; 2 marginally satisfactory; 3 neutral; 4 satisfactory; 5 very satisfactory. Higher scores mean a better outcome.
7 weeks
Classroom climate/atmosphere
Time Frame: 13 weeks
Questionnaire created by the National Education. Items will be rated from 1 to 5: 1 unsatisfactory; 2 marginally satisfactory; 3 neutral; 4 satisfactory; 5 very satisfactory. Higher scores mean a better outcome.
13 weeks
Possible factors of failure of the strategy
Time Frame: 13 weeks
Questionnaire: socioeconomical level of parents, reason for refusal to participate , parents feeling, students feeling, teachers feeling. Higher scores mean a better outcome.
13 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Actual)

April 12, 2021

Primary Completion (Actual)

June 25, 2021

Study Completion (Actual)

June 25, 2021

Study Registration Dates

First Submitted

April 14, 2021

First Submitted That Met QC Criteria

May 5, 2021

First Posted (Actual)

May 11, 2021

Study Record Updates

Last Update Posted (Actual)

May 26, 2022

Last Update Submitted That Met QC Criteria

May 25, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • RBHP 2021 DUCLOS
  • 2021-A00114-37 (Other Identifier: 2021-A00114-37)

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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