- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04048967
Active Learning Norwegian Preschool(er)s (ACTNOW)
Study Overview
Status
Intervention / Treatment
Detailed Description
There are growing concerns about low physical activity levels among preschoolers. As 97% of 3-5-year-olds in Norway attend preschool, preschools are unique arenas for intervention, laying the foundation for equitable development of health, human capital, and life opportunities. Yet, evidence of scalable, effective and sustainable interventions to increase physical activity and concomitant outcomes in preschoolers is lacking. Specifically, there is a need to study how the purposeful use of the preschool instructional context can be used to increase moderate-to-vigorous physical activity across a wide range of motor competences to enhance development, cognitively engaging play, and physically active learning. These aspects, in combination, have the potential to simultaneously affect various developmental and learning outcomes, but implementing such a program requires a highly coordinated effort by highly trained individuals. Therefore, the aim of this study is to investigate the effects of an education module, which is designed to result in highly competent preschool staffs having a good understanding of development of motor competence, provision of cognitively engaging play, physically active learning, and pedagogic/didactic approaches and teaching principles to foster physically active and learning preschoolers, on child developmental outcomes. Hopefully, this professional development will promote a physically active lifestyle in the early years that will favorably influence cognition and learning, and provide an efficient, acceptable, and feasible venue to build human capital and provide an early solution to lifelong public health and developmental challenges.
Two main research questions will be tested using both quantitative and qualitative methods, applied to both the child and organizational levels: 1) How does the intervention affect children's physical activity, physical fitness, motor competence, socio-emotional health, self-regulation, executive functions, and learning? 2) How does the intervention interact with different preschool contexts to produce various individual and organizational outcomes?
The proposed research questions will be investigated using a cluster RCT with randomization at the preschool level, including short- (6-month) and long-term (18-month) follow-up. The intervention development will include strong involvement from preschool owners and staff to provide broad support and anchor the project in the preschool sector. Thus, the investigators aim to combine a large-scale experimental study with continuous improvement effort in this sector allowing each preschool's contextual factors to be reflected within the larger cluster RCT. In this model, to make adaptations within each preschool is not considered a lack of fidelity; rather it is a desired process of institutionalization that balances internal and external validity. This balance also overcomes a common criticism of clinical trials as it increases the value for later scaling and dissemination to the real-world settings. In this way, the aim is to create sustainable solutions for improved child development and public health that can be disseminated in the long-term. Thus, the intervention's development, implementation, and evaluation are framed within a "realist RCT" approach. The intervention model is further framed within a socioecological model, placing the preschool as an influential factor for children's health and development. The intervention has two levels; the preschool level and the child level. In response to the challenge of low staff qualifications to implement physical activity, the main component will be a 7-month professional development offered to preschool staff. The intervention is structured as a 15-credit continuing education module that provide staff the opportunity to achieve credits for their efforts. The study is based on the logic model that this professional development will change preschool practices, which will in turn increase and improve children's physical activity opportunities and levels and lead to child developmental effects. Thus, the main aim of the professional development is to provide preschool staff the necessary expertise and resources to intervene on the child level. Researchers will not directly take part in the delivery of the intervention on the child level. The intervention at the child level is derived from hypotheses, theory and evidence relating to the beneficial effects of physical activity on physical, socio-emotional, and cognitive development and have four core components. Central to the ACTNOW intervention is opportunities for children to engage in a variety of meaningful physically active play that brings joy and supports the development of the whole child. By the integration of the four core components, the aim is to provide children opportunities to increase moderate-to-vigorous physical activity across a wide range of motor competencies to enhance development, cognitive engaging play/games, and physically active learning. As such, the core components and dosages promoted are 1) developmentally appropriate moderate-to-vigorous physical activity (60 min/day), 2) motor challenging physical activity (90 min/week), 3) cognitive engaging play/games (90 min/week), and 4) physical activity integrated with learning activities (90 min/week). The intervention will be delivered by the preschool teachers and staff through the use of a wide specter of types of physically active play; from child-initiated and directed free-play at the one end, to adult-initiated child-directed guided play, and adult-directed and initiated structured teacher-led physical activity at the other end.
The study have 2 waves, the first running from August 2019 to June 2021, and the second from August 2020 to June 2022. The professional development provided in Wave 2 will be adjusted based on experiences and findings from Wave 1. Data collection will have 3 main phases; pre-testing performed before randomization, 6-month follow-up performed at the end of the professional development, and 18-month follow-up performed 1 year after completing the professional development. In addition, process evaluation measures will be taken throughout the study.
Derived from a conservative sample size calculation using standard formulas, including correction for the cluster RCT design, it is an aim to recruit a minimum of 60 preschools and 1200 children to the study. This sample size will allow for uncovering statistical significant standardized effect sizes (Cohen's d) of 0.25-0.30.
A range of measures will be taken to examine the interventions effectiveness on a child level (physical activity, physical fitness, motor skills, adiposity, socio-emotional health, self-regulation, executive functions, and learning) and to describe the implementation and adaptation processes taking place in the preschools over 18 months. The realist evaluation includes both quantitative and qualitative data.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Sogndal, Norway, 6856
- Western Norway University of Applied Sciences
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Attending a participating preschool
- Born in 2014, 2015 or 2016 (wave 1) OR 2015, 2016, or 2017 (wave 2)
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention
Preschool staffs will participate in 50 hours of professional development over 7 months focused on promotion of physical activity in the preschool setting.
Staffs and investigators will work together to develop models to ensure children receive 60 minutes per day of moderate-to-vigorous physical activity, 90 minutes per week of motor challenging physical activity, 90 minutes per week of cognitively engaging games/play, and 90 minutes per week of physically active learning.
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professional development of preschool staff
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No Intervention: Control
Staffs receive no professional development and children will receive standard care.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Executive function
Time Frame: Change to 18 months
|
Inhibition, working memory, and cognitive flexibility by the Early Years Toolbox
|
Change to 18 months
|
Executive function
Time Frame: Change to 6 months
|
Inhibition, working memory, and cognitive flexibility by the Early Years Toolbox
|
Change to 6 months
|
Learning
Time Frame: Change to 18 months
|
Early math skills and expressive vocabulary by the Early Years Toolbox
|
Change to 18 months
|
Learning
Time Frame: Change to 6 months
|
Early math skills and expressive vocabulary by the Early Years Toolbox
|
Change to 6 months
|
Children's socio-emotional health
Time Frame: Change to 18 months
|
Child Self-regulation and Behavior Questionnaire (CSBQ), Early Years Toolbox.
Includes 33 items rated 1-5 across subscales of cognitive self-regulation, behavioral self-regulation, emotional self-regulation, sociability, prosocial behavior, externalizing problems, and internalizing problems.
|
Change to 18 months
|
Children's socio-emotional health
Time Frame: Change to 6 months
|
Child Self-regulation and Behavior Questionnaire (CSBQ), Early Years Toolbox.
Includes 33 items rated 1-5 across subscales of cognitive self-regulation, behavioral self-regulation, emotional self-regulation, sociability, prosocial behavior, externalizing problems, and internalizing problems.
|
Change to 6 months
|
Children's self-regulation
Time Frame: Change to 18 months
|
Head-Toes-Knees-Shoulders task (HTKS)
|
Change to 18 months
|
Children's self-regulation
Time Frame: Change to 6 months
|
Head-Toes-Knees-Shoulders task (HTKS)
|
Change to 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Children's physical activity
Time Frame: Change to 18 months
|
ActiGraph GT3X+
|
Change to 18 months
|
Children's physical activity
Time Frame: Change to 6 months
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ActiGraph GT3X+
|
Change to 6 months
|
Children's aerobic fitness, muscle strength and power, and speed-agility
Time Frame: Change to 18 months
|
PREFIT test battery
|
Change to 18 months
|
Children's aerobic fitness, muscle strength and power, and speed-agility
Time Frame: Change to 6 months
|
PREFIT test battery
|
Change to 6 months
|
Children's motor skills
Time Frame: Change to 18 months
|
Standardized observation and scoring tool guided by Test of Gross Motor Development-3 and the Preschooler Gross Motor Quality Scale including a total of 9 tasks across locomotor, object control, and balance skills.
|
Change to 18 months
|
Children's motor skills
Time Frame: Change to 6 months
|
Standardized observation and scoring tool guided by Test of Gross Motor Development-3 and the Preschooler Gross Motor Quality Scale including a total of 9 tasks across locomotor, object control, and balance skills.
|
Change to 6 months
|
Children's waist circumference
Time Frame: Change to 18 months
|
Cm
|
Change to 18 months
|
Children's waist circumference
Time Frame: Change to 6 months
|
Cm
|
Change to 6 months
|
Children's body mass index
Time Frame: Change to 18 months
|
Calculated from body mass (kg) and height (m); kgm2
|
Change to 18 months
|
Children's body mass index
Time Frame: Change to 6 months
|
Calculated from body mass (kg) and height (m); kgm2
|
Change to 6 months
|
Staffs' physical activity
Time Frame: Change to 18 months
|
ActiGraph GT3X+
|
Change to 18 months
|
Staffs' physical activity
Time Frame: Change to 6 months
|
ActiGraph GT3X+
|
Change to 6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Eivind Aadland, PhD, Western Norway University of Applied Sciences
Publications and helpful links
Helpful Links
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
Keywords
Other Study ID Numbers
- ACTNOW
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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