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PA4WELL primary schools program: a study to increase students’ cardiorespiratory fitness and contribute their physical, social and mental health

PA4WELL primary schools program: a hybrid effectiveness -implementation trial to increase students’ cardiorespiratory fitness and contribute their physical, social and mental health

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10820452
Enrollment
1200
Registered
2026-06-25
Start date
2026-08-02
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiorespiratory fitness, physical activity and physical, mental, and social health and well-being among primary school children. Other

Interventions

This study is a three-arm cluster randomized controlled trial conducted in 30 Finnish primary schools including approximately 1200 Grade 5 students (aged ~11 years), their teachers, school principals,

Sponsors

University of Jyväskylä
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 14 Years

Inclusion criteria

Inclusion criteria: 1. Grade 5 students (typically aged 11-12 years) enrolled in participating primary schools in Central Finland 2. Primary schools in Central Finland with Grade 5 classes 3. Principals of participating primary schools in Central Finland 4. Grade 5 teachers and, where applicable, physical education (PE) teachers responsible for teaching PE to Grade 5 students in participating schools 5. Legal guardians of participating students

Exclusion criteria

Exclusion criteria: 1. Schools with combined classes (e.g. 5-6) 2. Special schools and teacher training schools 3. Schools with a specific focus on sports 4. Individuals unable to participate in study procedures or provide informed consent (for example, due to insufficient language proficiency)

Design outcomes

Primary

MeasureTime frame
Cardiorespiratory fitness (students) measured using 20-metre shuttle run test (number of laps completed) at baseline, 7 months (post-intervention), and 19 months (follow-up)

Secondary

MeasureTime frame
Physical activity (students) measured using Actigraph wGT3X-BT accelometer (7 days) at baseline, 7 months (post-intervention), and 19 months (follow-up);Recovery during the day and sleep (students) measured using Firstbeat Bodyguard 3 heart rate variability measurement (5 days) at baseline, 7 months (post-intervention), and 19 months (follow-up);Well-being (students) measured using WHO-5 Well-Being Index at baseline, 7 months (post-intervention), and 19 months (follow-up);Mental and social health (students) measured using Strengths and Difficulties Questionnaire (SDQ) at baseline, 7 months (post-intervention), and 19 months (follow-up);School engagements (students) measured using Study Engagement Scale at baseline, 7 months (post-intervention), and 19 months (follow-up);Study burnout (students) measured using Study Burnout Inventory at baseline, 7 months (post-intervention), and 19 months (follow-up);Self-reported physical activity (students) measured using Two-item physical activity questionnaire at baseline, 7 months (post-intervention), and 19 months (follow-up);Perceived physical competence (students) measured using Sport competence subscale of the Physical Self-Perception Profile at baseline, 7 months (post-intervention), and 19 months (follow-up);Body mass index (students) measured using weight and height at baseline, 7 months (post-intervention), and 19 months (follow-up);Parental support for children’s physical activity (guardians) measured using Family Physical Activity Environment questionnaire at baseline, 7 months (post-intervention), and 19 months (follow-up);Implementation of whole-of-school physical activity components measured using number of components implemented in previous month at 7 months (post-intervention), and 19 months (follow-up);Teachers’ capability, opportunity, and motivation to implement the intervention measured using COM-PASS scale at baseline, 7 months (post-intervention), and 19 months (follow-up)

Countries

Finland

Contacts

Public ContactTimo Jaakkola
timo.jaakkola@jyu.fi+358408053949

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jul 23, 2026