- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05359536
Training Early Childhood Educators to Increase Children's Physical Activity: The TEACH-Preschooler Study
Impact of an Early Childhood Educator e-Learning Course in Physical Activity and Sedentary Behaviour on Young Children's Movement Behaviours in Childcare: The TEACH-Preschooler Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In this cluster randomized controlled trials, early childhood educators from childcare centres in London, Ontario, Canada will be randomized to complete a 4 module e-learning course with content on physical activity and sedentary guidelines, physical activity and sedentary behaviours in the childcare environment, how to promote physical activity and reduce sedentary behaviours in young children, and a resource library, or to continue with their usual practices. Early childhood educators randomized to the intervention group will be asked to complete this course over a 2-week intervention period.
In both the intervention and control groups, preschoolers physical activity and sedentary behaviours will be measured at baseline, post-intervention (2-weeks) and 3-months follow-up using Actigraph GT3X+ accelerometers. Preschoolers will also complete tasks at baseline and 3-month follow-up to measure their cognitive development, and a subgroup of randomly selected children from each group will complete the Tests of Gross Motor Development - Third Edition to assess their fundamental movement skill proficiency at baseline and follow-up. Parents of children in both groups will complete a questionnaire to measure their perception of their children's proficiency at fundamental movement skills. Parents will also be asked to report on their child's emotional symptoms, conduct problems, hyperactivity/inattention, peer relationship problems and prosocial behaviours by completing the Strength and Difficulties Questionnaire
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ontario
-
London, Ontario, Canada
- Child Health and Physical Activity Lab
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Childcare Centres:
- Located in London, ON, Canada
- Have at least 1 preschool classroom
- Open every weekday
- Operate for at least 8 hours on weekdays
- All early childhood educators are willing to participate in the study
- Staff are English speaking
Early Childhood Educators:
- Employed at a participating childcare centre
- English speaking
Children:
- Enrolled at a participating childcare centre
- Between the ages 2.5-5 years at baseline
- Are expected to remain at the childcare centre for the duration of the study period
Exclusion Criteria:
Childcare Centres:
- Not located in London, ON, Canada
- Do not have at least 1 preschool classroom
- Not open every weekday
- Do not operate for at least 8 hours on weekdays
- Not all early childhood educators are willing to participate in the study
- Staff do not speak English
Early Childhood Educators:
- Not employed at a participating childcare centre
- Do not speak English
Children:
- Not enrolled at a participating childcare centre
- Not between the ages 2.5-5 years at baseline
- Not expected to remain at the childcare centre for the duration of the study period
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: E-learning Intervention
Early career educators in the intervention condition will be asked to complete a 5-hour e-learning course over a two week timeframe.
The four module e-learning course was developed using the Delphi technique and covers physical activity and sedentary guidelines, physical activity and sedentary behaviours in the childcare environment, how to promote physical activity and reduce sedentary behaviours in young children, and a resource library.
|
The four module e-learning course was developed using the Delphi technique and covers physical activity and sedentary guidelines, physical activity and sedentary behaviours in the childcare environment, how to promote physical activity and reduce sedentary behaviours in young children, and a resource library.
|
|
No Intervention: Usual Practice Control
Early career educators in the control condition will be asked to continue with their usual practices.
They will be invited to complete the e-learning course after the study period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in children's device measured moderate-to-vigorous physical activity while at childcare measured
Time Frame: Baseline, post-intervention (2-weeks), and 3-months follow-up
|
Assessed using ActiGraph GT3X+ accelerometers worn on each child's right hip for 5 consecutive days (Monday-Friday) while at childcare.
Age-specific validated accelerometer cut-points will be used to calculate time spent in moderate-to-vigorous physical activity (i.e.
>420 counts/15-second epoch).
Children will be considered to have valid accelerometer data if they have at least 5 hours of accelerometer data on 2 days.
Accelerometer non-wear time will be identified as any period with 20 consecutive minutes of zero counts.
|
Baseline, post-intervention (2-weeks), and 3-months follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in children's device sedentary behaviours while at childcare
Time Frame: Baseline, post-intervention (2-weeks), and 3-months follow-up
|
Assessed using ActiGraph wGT3X-BT accelerometers worn on each child's right hip for 5 consecutive days (Monday-Friday) while at childcare.
Age-specific validated accelerometer cut-points will be used to calculate time spent in moderate-to-vigorous physical activity (i.e.
<48 counts/15-second epoch).
Children will be considered to have valid accelerometer data if they have at least 5 hours of accelerometer data on 2 days.
Accelerometer non-wear time will be identified as any period with 20 consecutive minutes of zero counts.
|
Baseline, post-intervention (2-weeks), and 3-months follow-up
|
|
Change in children's fundamental movement skills
Time Frame: Baseline and 3-months follow-up
|
Assessed in a sub-sample of randomly selected children using the Test of Gross Motor Development - Third Edition.
Test of Gross Motor Development - Third Edition tests six locomotor skills (run, gallop, hop, skip, jump, and slide) and 7 object control skills (two handed strike, forehand strike, dribble, catch, kick, overhand throw, and underhand throw).
Each skill was assessed and scored twice on between 3-5 performance criteria where a child was given a 1 if the skill is performed correctly and a 0 if performed incorrectly.
A total score between 0-100 is calculated with a higher score indicating a better outcome.
|
Baseline and 3-months follow-up
|
|
Change in parent's perceptions of fundamental movement skill proficiency
Time Frame: Baseline and 3-months follow-up
|
Parents of children will be asked to report their perceptions of their child's fundamental movement skills.
The self-reported scale will measure the same 13 fundamental movement skills measured in the Test of Gross Motor Development - Third Edition.
The will rate their Childs proficiency for each skill on a scale from 1 = not that good, 2 = sort of good, 3 = pretty good and 4 = really good.
Eah skill is presented with a picture of the skill being performed.
The range of possible scores for this scale are 13-52, with higher scores indicating a better outcome.
|
Baseline and 3-months follow-up
|
|
Changes in scores on the Strengths and Difficulties Questionnaire
Time Frame: Baseline and 3-months follow-up
|
Parents will report on their child's emotional symptoms, conduct problems, hyperactivity/inattention, peer relationship problems and prosocial behaviours.
Each item is scored on a scale from 0 =not true, 1 =somewhat true, and 2 = certainly true, with positively worded questions being reversed scored for the emotional symptoms, conduct problems, hyperactivity/inattention, and peers relationship problem subscales.
Higher scores on these four subscales indicates a worse outcome, while a higher score on the emotional symptoms subscale indicates a better outcome.
Each subscale is scored on a scale from 0-10.
|
Baseline and 3-months follow-up
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- R4368A35
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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