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Active, not recruitingNCT07737548OLYMPIC-SUpdated Jul 31, 2026

OLYMPIC-S: Outcomes of a Life-stYle Multicomponent Physical-activity Intervention in Children at School

An interventional study of Olympic School in Physical Inactivity, Health Behavior and Child Health, sponsored by Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina. Active, not recruiting at 1 site in Spain. Open to participants aged 8 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-31.

Sponsored by Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Feb 2026, registered Jul 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
893
Allocation
Randomized
Ages
8 Years to 12 Years
Sex
All
01

Study summary

OLYMPIC-S is a cluster randomized controlled trial evaluating a four-month school-based intervention designed to increase moderate-to-vigorous physical activity and promote healthy habits among children in the fourth, fifth and sixth grades of primary school. Fifteen schools and approximately 1,200 children will participate. Schools will be randomized to the Olympic School intervention or to a control group continuing usual school activities.

Intervention schools will introduce 15 minutes of physical activity during each school day. Teachers may choose between outdoor walking or running activities based on The Daily Mile or structured movement video sessions from the Born to Move programme. A gamified web platform will record the activity performed, display each school's collective progress through an Olympic journey, unlock educational content and reinforce messages related to physical activity, healthy eating, hydration and sleep.

Outcomes will be assessed at baseline and immediately after the four-month intervention. The primary outcome is daily moderate-to-vigorous physical activity measured using the PAU-7S questionnaire. Secondary outcomes include dietary habits, fruit and water consumption, sleep, emotional well-being, health-related quality of life, adherence, platform use, feasibility and acceptability. Post-intervention focus groups with children and teachers will complement the quantitative evaluation.

Read the detailed description

Regular physical activity is important for children's physical and emotional development, but many children do not achieve recommended physical activity levels. Schools provide an appropriate environment for introducing regular opportunities for movement and for promoting healthy behaviours. Olympic School programme combines a brief daily physical activity component with gamification and health-promotion messages intended to support participation and sustained engagement.

This study will use a two-arm cluster randomized controlled design, with the school as the unit of randomization. Fifteen primary schools will be allocated to the intervention or control condition. Children in the fourth, fifth and sixth grades whose parents or legal guardians provide informed consent and who provide assent will be invited to participate in the study assessments.

For four months, intervention schools will incorporate 15 minutes of physical activity into each school day. Schools may select the time of day that is most compatible with their routine. Teachers may conduct outdoor walking or running sessions based on The Daily Mile programme or use structured movement video sessions from the Born to Move programme. The intervention is supported by a gamified web platform presenting participation as a collective journey towards the Olympic Games. The platform records activity minutes, displays progress, unlocks Olympic cities and educational content, and provides brief messages relating to physical activity, diet, hydration and sleep. Control schools will continue their usual school activities and will not have access to the intervention platform during the study period.

Quantitative assessments will be completed at baseline and immediately after the four-month intervention. The primary outcome will be moderate-to-vigorous physical activity measured using PAU-7S. Secondary outcomes will assess Mediterranean diet adherence, fruit and water consumption, sleep, emotional well-being and health-related quality of life. Platform data will be collected throughout the intervention to evaluate implementation and adherence.

Quantitative analyses will follow the intention-to-treat principle. Mixed-effects models will account for repeated measurements and the clustering of participants within schools and will include study group, time, the group-by-time interaction and baseline outcome values. Sensitivity analyses will assess the effect of missing data. Post-intervention focus groups with children and teachers from intervention schools will explore acceptability, perceived benefits, implementation barriers and opportunities for improvement. Qualitative data will be analysed thematically and integrated with the quantitative and platform-use findings.

02

Conditions studied

  • Physical Inactivity
  • Health Behavior
  • Child Health

Keywords

  • School-based intervention
  • Physical activty
  • Moderate-to-vigorous physical activity
  • MVPA
  • Gamification
  • Healthy lifestyle
  • Primary school
  • Children
  • Childhood obesity prevention
  • Implementation research
  • Intervention adherence
03

In context

Sedentary Behavior

332 studies on the registry are indexed under Sedentary Behavior; 155 are open to participants now.

This study's enrollment of 893 is above the median of 70 across 287 interventional studies indexed under Sedentary Behavior.

Browse Sedentary Behavior studies →

Lead sponsor

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina is the lead sponsor of 158 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
8 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

The intervention content is intended for approximately 8-12-year-old children, but the actual lower and upper age limits should be based on the expected ages of pupils in the participating fourth-, fifth- and sixth-grade classes.

Inclusion Criteria:

  • Enrolled in the fourth, fifth or sixth grade at a participating primary school.
  • Parent or legal guardian has provided written informed consent.
  • Child has provided informed assent.
  • Child is able to complete the study questionnaires with the support normally available during classroom administration.
  • Child is expected to remain enrolled at the participating school throughout the four-month intervention period.

Exclusion Criteria:

  • Written parental or legal-guardian consent has not been obtained.
  • The child does not provide assent or withdraws assent.
  • The child cannot participate in the study assessments according to the criteria established in the approved protocol.

Teacher focus-group eligibility:

Inclusion criteria:

  • Teachers or other school staff who directly participated in implementing Olympic School at an intervention school and who provide written informed consent.

Exclusion criteria:

  • Teachers or school staff who did not participate directly in implementation or who do not consent to the audio-recorded focus group.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
893 participants (actual)

Study arms

  • Experimental
    Olympic School intervention

    Schools allocated to the experimental group will implement the Olympic School programme for four months. On each school day, participating classes will undertake 15 minutes of teacher-led physical activity. Teachers may choose between outdoor walking or running based on The Daily Mile principles or structured movement video sessions from Born to Move programme. The activity will be supported by a gamified web platform that records activity minutes, displays collective progress through an Olympic journey, unlocks cities and educational materials, and presents brief health messages concerning physical activity, fruit consumption, hydration and sleep. Schools will also receive a physical progress poster and symbolic recognition will be provided at the end of the programme.

    Behavioral: Olympic School

  • No intervention
    Usual School Activities

    Schools allocated to the control group will continue their usual educational and physical activity practices. They will not have access to the Olympic School web platform during the four-month study period.

Interventions

  • BehavioralOlympic School

    A four-month multicomponent school-based behavioural intervention consisting of 15 minutes of physical activity during each school day, supported by a gamified digital platform, collective progress monitoring, educational health messages and motivational rewards.

06

What researchers measure

Primary outcomes

  1. Change From Baseline in Daily Moderate-to-Vigorous Physical Activity at 4 Months

    Moderate-to-vigorous physical activity will be assessed using the PAU-7S questionnaire. The outcome will be expressed as the estimated mean number of minutes per day spent in moderate-to-vigorous physical activity. Higher values indicate more physical activity. The primary comparison will be the adjusted difference in change from baseline between intervention and control groups, accounting for the clustering of participants within schools.

    Time frame: Baseline and immediately after the four-month intervention

Secondary outcomes

  1. Change From Baseline in Mediterranean Diet Adherence at 4 Months

    Mediterranean diet adherence will be measured using the KIDMED 2.0 questionnaire. The total score and its interpretation will be calculated according to the validated scoring instructions. Higher scores are expected to indicate greater adherence to a Mediterranean dietary pattern.

    Time frame: Baseline and immediately after the four-month intervention

  2. Change From Baseline in Fruit Consumption at 4 Months

    Fruit consumption will be assessed using the specific fruit-consumption questions included in the study questionnaire and reported as the average number of fruit servings consumed per day. Higher values indicate greater daily fruit consumption.

    Time frame: Baseline and immediately after the four-month intervention

  3. Change From Baseline in Water Intake at 4 Months

    Water intake will be assessed using the specific hydration questions included in the study questionnaire and reported as the average number of glasses of water consumed per day. Higher values indicate greater daily water intake.

    Time frame: Baseline and immediately after the four-month intervention

  4. Change From Baseline in Sleep-Related Problems at 4 Months

    Sleep-related problems will be assessed using the BEARS Sleep Screening Tool, covering bedtime problems, excessive daytime sleepiness, awakenings during the night, regularity and duration of sleep, and snoring. Outcomes will be calculated according to the prespecified study scoring approach.

    Time frame: Baseline and immediately after the four-month intervention

  5. Change From Baseline in Sleep Duration at 4 Months

    Average sleep duration will be reported in hours per night based on responses to the study sleep questionnaire. Higher values indicate longer sleep duration.

    Time frame: Baseline and immediately after the four-month intervention

  6. Change From Baseline in Health-Related Quality of Life at 4 Months

    Health-related quality of life and emotional well-being will be measured using KIDSCREEN-10. Scores will be calculated according to the validated scoring procedure. Higher scores indicate better health-related quality of life.

    Time frame: Baseline and immediately after the four-month intervention

  7. Number of School Physical Activity Sessions Completed During the Intervention

    The web platform will automatically record the number of physical activity sessions registered by each participating class and school during the four-month intervention.

    Time frame: Continuously during the four-month intervention

  8. Adherence to the Olympic School Intervention

    Intervention adherence will be calculated as the number or percentage of eligible school days on which a participating class registers completion of the planned 15-minute physical activity session.

    Time frame: Throughout the four-month intervention

  9. Engagement With the Gamified Web Platform

    Platform engagement will be assessed using automatically recorded indicators, including the number of educational videos viewed, number of Olympic cities unlocked, progression through the gamified journey and frequency of platform use.

    Time frame: Throughout the four-month intervention

Other outcomes

  1. Acceptability and Feasibility of the Escola Olímpica Intervention

    Acceptability and feasibility will be explored through post-intervention focus groups with participating children and teachers from intervention schools. Topics will include satisfaction, perceived benefits, barriers to implementation, use of the platform, integration into school routines and suggestions for improvement. Audio recordings will be transcribed, pseudonymized and analysed using thematic analysis.

    Time frame: Immediately after completion of the four-month intervention

07

Study locations

1 site
  • IDIAPJGol
    Barcelona, Barcelona 08007, Spain
08

References and documents

Individual participant data

Plan to share: Undecided — Individual participant data are not currently planned for public sharing because the study involves minors and school-level clusters, which may create a risk of participant or school re-identification. Aggregated and anonymized study findings will be disseminated through scientific publications and project reports. Requests for access to suitably de-identified data may be considered in accordance with the informed consent, ethics approval, data protection legislation and the PREVENT Data Management Plan.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07737548
Lead sponsor
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Collaborators
Department of Health, Generalitat de Catalunya
Responsible party
Sponsor
First posted
Jul 30, 2026
Start date
Feb 2, 2026
Primary completion
Sep 2026 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Jul 31, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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