Influence of Preschool Children's Fundamental Movement Skills, Physical Activity, and Physical Fitness on Executive Function: A Prospective Observation Study
13 maart 2022 bijgewerkt door: Hong Kong Baptist University
Background: Early childhood is the most critical and rapid period of complete and healthy physical and cognitive development in human life. Executive function appears in early childhood and develops rapidly through complex coaction between environment and developmental processes. The preschool period is also characterized by a rapid growth in fundamental movement skills, physical activity and physical fitness. The scientific research on the relationship between fundamental movement skills, physical activity, physical fitness and executive function in preschoolers remains to be explored.
Objective: The purpose of this study was to examine the cross-sectional relationship between fundamental movement skills, physical activity, physical fitness and executive function in preschool children while controlling for potential confounding variables, examine the prospective influence (independent and interactive role) of preschooler's fundamental movement skills, physical activity and physical fitness on executive function, observe the preschoolers' fundamental movement skills, physical activity, physical fitness and executive function changes with age, and investigate gender and age differences in preschoolers' fundamental movement skills, physical activity, physical fitness and executive function.
Method: The proposed study consists of two phases, phase 1 is a cross-sectional study. Five hundred and five children aged 3-5 years will be recruited. The Test of Gross Motor Development Third Edition (TGMD-3) was used to assess children's fundamental movement skills. Preschool children's physical activity was monitored by accelerometer ActiGraph GT3X-BT. Physical fitness was tested using handgrip, 4*10m shuttle run, 20m shuttle run, 30s sit-ups, sit and reach, and balance beam. Executive function was tested by computer-based tasks including animal stroop, safari training and stop signal task. Phase 2 is a 12-month follow-up study. In the phase 2, all children enrolled in the baseline study will be followed up, the measurements and contents of the follow-up are the same as the baseline instrument.
Studie Overzicht
Toestand
Actief, niet wervend
Studietype
Observationeel
Inschrijving (Verwacht)
505
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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Guangdong
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Zhuhai, Guangdong, China
- Beijing Normal University - Hong Kong Baptist University United International College
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Hong Kong
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Hong Kong, Hong Kong, China
- Hong Kong Baptist University
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
3 jaar tot 5 jaar (Kind)
Accepteert gezonde vrijwilligers
Ja
Geslachten die in aanmerking komen voor studie
Allemaal
Bemonsteringsmethode
Niet-waarschijnlijkheidssteekproef
Studie Bevolking
Children will be recruited from kindergartens in Zhuhai through the support of Zhuhai Early Childhood Education Association and United International College.
These two organizations have cooperated with many local kindergartens, which can help to recruit preschoolers.
Beschrijving
Inclusion Criteria:
- aged 3-5 years
- normally developing children with corresponding cognitive ability to participate in the data collection
- without heart, lung, liver, kidney and other important organ diseases or any neurological disorders (e.g., intellectual disability or autism spectrum disorder) that prevent children from performing normal PA.
Exclusion Criteria:
- children with cognitive disability
- with heart, lung, liver, kidney and other important organ diseases or any neurological disorders (e.g., intellectual disability or autism spectrum disorder) that prevent children from performing normal PA.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Change of body mass index
Tijdsspanne: through study completion, 12 months
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Weight (measured in kilograms) and height (measured in meters) will be combined to report body mass index in kg/m^2.
Change of body mass index between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of fundamental movement skills
Tijdsspanne: through study completion, 12 months
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The Test of Gross Motor Development: Third Edition (TGMD-3) will be used to assess children's fundamental movement skills.
The TGMD-3 provides two subscale and an overall composite score.
Change of fundamental movement skills between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of sedentary behavior time
Tijdsspanne: through study completion, 12 months
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Physical activity level will be objectively monitored using a tri-axial accelerometer ActiGraph GT3X-BT and is analyzed with the ActiLife 6.13 data analysis software.
Counts per minute are recorded.The activity with lower than 819 counts per minute is categorized as sedentary behaviors.
Overall time in sedentary behavior in minute is recorded as sedentary behavior time.
Change of sedentary behavior time between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of light physical activity time
Tijdsspanne: through study completion, 12 months
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Physical activity level will be objectively monitored using a tri-axial accelerometer ActiGraph GT3X-BT and is analyzed with the ActiLife 6.13 data analysis software.
Counts per minute are recorded.
The activity with higher than 820 counts per minute but lower than 3907 counts per minute is categorized as light physical activity.
Overall time in light physical activity in minute is recorded as light physical activity time.
Change of light physical activity time between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of moderate-to-vigorous physical activity time
Tijdsspanne: through study completion, 12 months
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Physical activity level will be objectively monitored using a tri-axial accelerometer ActiGraph GT3X-BT and is analyzed with the ActiLife 6.13 data analysis software.
Counts per minute are recorded.
The activity with higher than 3908 counts per minute is categorized as moderate-to-vigorous physical activity.
Overall time in moderate-to-vigorous physical activity in minute is recorded as moderate-to-vigorous physical activity time.
Change of moderate-to-vigorous physical activity time between baseline and post-intervention tests is assessed.
Change of moderate-to-vigorous physical activity time between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of cardiorespiratory fitness
Tijdsspanne: through study completion, 12 months
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A 20-meter shuttle run is used to assess cardiorespiratory fitness.
During the test, participants run back and forth on two running tracks 20 meters apart at an initial speed of 8.0km/h, followed by an increase of 0.5km/h per minute.
Using a compact disc (CD) to control the speed, which systematically increases during the test.
During the test, participants run back and forth, based on the timing of a beep from the CD recorder.
If the participant fails to pass the other end of the 20 meters distance before the beep (after two attempts), the test is terminated and the number of shuttle legs completed is recorded and converted to an estimate of aerobic capacity.
As we work with preschoolers, the track will be marked and the children will be led by an adult so they can master the pace of the run.
Change of cardiorespiratory fitness between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of flexibility
Tijdsspanne: through study completion, 12 months
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Flexibility will be assessed by sit and reach.
During the test, the participants sit barefoot on the mat, feet straight with heels together, toes separated naturally, and the sole of their feet on the tester plate.
Then the participant is asked to slowly bend forward and use their arms to push the edge of a movable board as far as they can without bending knees.
The test is repeated twice, and the maximum value is recorded.
Change of flexibility between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of muscular endurance
Tijdsspanne: through study completion, 12 months
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Sit ups will be used to assess the muscular endurance of the trunk.
The participants lie on their back with knees bent and arms crossed on the other shoulder.
They stand up, sit up, and return to the starting position.
The assistant holds the child's feet.
The number of lifts in 30 seconds performed correctly to the seated position is recorded.Change of muscular endurance between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of muscular strength
Tijdsspanne: through study completion, 12 months
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Hand grip strength is a classic strength test with high safety, accuracy, and suitability for younger children.
Muscle strength is measured using a WCS-100 electronic dynamometer (Shanghai Wanqing Electronics Co., LTD.).
During the test, participants stand in a quiet environment, relaxed, with their arms hanging down naturally.
They hold the dynamometer, adjust the grip distance, grasp the dynamometer once with maximum strength, and the value is recorded.
The left and right hands are measured alternately for three times, and the maximum value is recorded.
To allow for proper rest, the interval between the three tests should be at least 15 seconds.
Change of muscular strength between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of balance
Tijdsspanne: through study completion, 12 months
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Dynamic balance will be measured by the balance beam test.
The participants will stand on the platform behind the starting line, face the balance beam (3 m long, 10 cm wide, and 30 cm high), and raise their arms horizontally.
When participants hear the start command, they will move their feet to the finish line in turn.
The tester will give orders on the front side of the participant, start the stopwatch at the same time when the participant starts, and follow the participant to the finish line.
At the same time, the tester will pay attention to observe the movements of the participant to prevent accidents.
When either tiptoe of the participant crosses the finish line, the tester stops the clock immediately.
The test is repeated twice, and the best result is recorded.
Change of balance between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of speed-agility
Tijdsspanne: through study completion, 12 months
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Speed-agility will be assessed by the 4 × 10-meter shuttle run test.
When the participants hear the start signal, they run and turn a 10-meter track as fast as they can to cover a distance of 40 meters.
At the end of each section of the track, participants have to touch the hand of one of the testers who have crossed the limit with their feet and then go back at maximum speed.
The participant will be given two tests with one to two minutes breaks in between.
The best of two tests is recorded.
Change of speed-agility between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of inhibitory control
Tijdsspanne: through study completion, 12 months
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Animal Stroop task will be used to assess inhibitory control.
The reaction time difference between conflict and congruent conditions reflects the ability to handle cognitive conflicts.
Change of inhibitory control between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of cognitive flexibility
Tijdsspanne: through study completion, 12 months
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Stop-signal task will measure the ability to inhibit response and control impulsivity.
The mean stop-signal delay indicates the ability to inhibit portent responses.
Change of cognitive flexibility between baseline and follow-up test is assessed.
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through study completion, 12 months
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Change of working memory
Tijdsspanne: through study completion, 12 months
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Safari training task will measure working memory.
There are 90 trials in total and the task takes about 8 minutes.
Change of working memory between baseline and follow-up test is assessed.
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through study completion, 12 months
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Demographics questionnaire
Tijdsspanne: through study completion, 12 months
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Participant's background information (gender, age, gestational week, delivery mode, gestation, feeding mode, main caregivers), sleep, parental PA behaviors and attitudes, and family information (family economic status, parents' education level, family structure) are recorded.
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through study completion, 12 months
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Screen time
Tijdsspanne: through study completion, 12 months
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Screen time will be measured by the Parents' Role in Establishing healthy Physical activity and Sedentary behavior habits study (PREPS) questionnaire developed.
The weighted minutes per day for each variable are then summed to generate total screen time.
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through study completion, 12 months
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Sleep
Tijdsspanne: through study completion, 12 months
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Sleep will be assessed with the Children's Sleep Habits Questionnaire (CSHQ).
It contains 56 items, 52 of which are rated on a three-point Likert scale.
Each question is asked in relation to the previous one week.
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through study completion, 12 months
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
11 oktober 2021
Primaire voltooiing (Verwacht)
31 december 2022
Studie voltooiing (Verwacht)
30 juni 2023
Studieregistratiedata
Eerst ingediend
24 februari 2022
Eerst ingediend dat voldeed aan de QC-criteria
13 maart 2022
Eerst geplaatst (Werkelijk)
22 maart 2022
Updates van studierecords
Laatste update geplaatst (Werkelijk)
22 maart 2022
Laatste update ingediend die voldeed aan QC-criteria
13 maart 2022
Laatst geverifieerd
1 maart 2022
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- HKBU19481772
Plan Individuele Deelnemersgegevens (IPD)
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NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
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