The "11 for Health" Program Intervention and Its Impact on Polish Children (11FHPoland)

June 4, 2026 updated by: Adrian Drożdżowski, Wroclaw University of Health and Sport Sciences

The "11 for Health" Program and Its Impact on Physical Fitness, Health Status, Health Knowledge, and Pro-Health Behaviors of Children in Poland

This study evaluates the impact of the "11 For Health" program-an innovative football-based health education initiative-on children's physical fitness, health status, health knowledge, and pro-health behaviors. Originally implemented in African and South American countries, the program has been adapted and successfully introduced in European and Asian countries. The intervention consists of structured football sessions integrating health education messages aimed at promoting a healthy lifestyle among schoolchildren. The study aims to evaluate the effectiveness of this program in enhancing both physical fitness and health-related outcomes in comparison to traditional physical education classes

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This randomized controlled trial (RCT) will include children from schools that have volunteered to participate in the project. These schools will be assigned to clusters, which will then be randomly allocated to one of two groups: the control group, following the standard physical education curriculum, or the intervention group, participating in the "11 For Health" program over an 11-week period (two sessions per week, 45 minutes each). Within each school, all students in a given cluster will be assigned to the same group to ensure consistency and minimize potential contamination.

Structure of the "11 For Health" Program The "11 For Health" programis a football-based program combined with structured health education content which consists of 11 structured sessions, each lasting 90 minutes and divided into two parts: • "Play Football" - A practical football-based component where children engage in skill-building exercises such as passing, dribbling, and shooting. • "Play Fair" - A theoretical component focused on health education, where key health-related topics (e.g., nutrition, hygiene, physical activity) are introduced through interactive discussions and activities.A new football-related topic paired with an appropriate health message will be discussed each week. Each session follows a standardized manual that outlines learning objectives, football exercises, and health messages. The program is designed to foster both physical engagement and health awareness, reinforcing messages through active participation. Children in the intervention group will participate in the "11 For Health" program during their weekly physical education lessons. In the Polish education system, children typically have 180 minutes of physical education per week. Of this, 90 minutes will be dedicated to the "11 For Health" program, while the remaining time will be spent on the standard physical education curriculum. This will allow for a direct comparison of the impacts of the program against the standard curriculum.

Participants will undergo baseline (pre-test) and post-intervention (post-test) assessments to evaluate physical fitness, health-related knowledge, wellbeing, body composition, health status, and pro-health behaviors. Physical tests and questionnaires will be used to measure outcomes. Physical fitness will be assessed using tests evaluating balance, muscular strength, aerobic capacity, agility, and endurance. Body composition will be analyzed through anthropometric measurements and bioelectrical impedance analysis (BIA), while cardiovascular health will be evaluated by measuring resting heart rate and blood pressure. Health-related knowledge, wellbeing, dietary habits, and physical activity levels will be assessed using questionnaires. Following the intervention, children in the experimental group will report their level of enjoyment of the program and football in general using a 5-point Likert scale. Teachers will complete questionnaires assessing program feasibility, acceptability, and implementation challenges. After the program's completion and data collection, a comparative analysis of the results from both groups will be conducted to determine the impact of the "11 For Health" program in improving physical fitness, health knowledge, health status, overall well-being and pro-health behaviors.

Study Type

Interventional

Enrollment (Actual)

663

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Lower Silesian Voivodeship
      • Wroclaw, Lower Silesian Voivodeship, Poland, 53-633
        • Wroclaw University of Health and Sport Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age between 9 and 14 years,
  • Signed informed consent from a parent or legal guardian for underage participants.

Exclusion Criteria:

  • Disabilities.
  • Medical contraindications.
  • Medical or other exemptions from physical education classes.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Standard Physical Education (Control group)
Participants will participate in standard physical education (PE) classes with no additional interventions.
Experimental: "11 For Health" Program (Intervention group)
Participants will participate in the "11 For Health" program, consisting of 11 sessions over 11 weeks. The program combines football skills with health education to promote overall health and well-being.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Health Knowledge
Time Frame: Baseline and after 3 months (post-intervention)
Health knowledge will be assessed using the "11 For Health" Health Knowledge Questionnaire. This questionnaire evaluates children's understanding of key health topics, including nutrition, physical activity, and hygiene. It consists of multiple-choice questions, aimed at measuring the knowledge acquired during the program. Higher scores indicate greater health knowledge (min= 0, max= 36)
Baseline and after 3 months (post-intervention)
Wellbeing
Time Frame: Baseline and after 3 months (post-intervention)
Wellbeing will be assessed using the Kidscreen-27 questionnaire, which evaluates emotional well-being, social functioning, and general life satisfaction. It uses a Likert scale to assess happiness, relationships with family, and feelings of self-worth, capturing the child's overall perception of their quality of life. Higher scores indicate better well-being. Higher scores indicate better well-being (Minimum = 27, Maximum = 135).
Baseline and after 3 months (post-intervention)
Yo-Yo Intermittent Recovery Test Level 1 (YYIR1C)
Time Frame: Baseline and after 3 months (post-intervention)
Aerobic fitness and endurance will be assessed using the Yo-Yo Intermittent Recovery Test Level 1 (YYIR1C), which measures the total distance covered in a repeated sprint and recovery format. A greater distance (meters [m]) indicates better aerobic capacity.
Baseline and after 3 months (post-intervention)
Stork Balance Test
Time Frame: Baseline and after 3 months (post-intervention)
Balance performance will be assessed using the Stork Balance Test, which evaluates single-leg balance ability. Time held in seconds ( higher scores indicate better balance).
Baseline and after 3 months (post-intervention)
Standing Long Jump Test
Time Frame: Baseline and after 3 months (post-intervention)
Lower body explosive strength will be assessed using the Standing Long Jump Test, measuring the horizontal distance jumped from a standing position with hands positioned on hips. A longer (centimeters [cm]) jump indicates better lower-body power
Baseline and after 3 months (post-intervention)
Hand Grip Test
Time Frame: Baseline and after 3 months (post-intervention)
Muscular strength will be assessed using the Hand Grip Test, which measures maximal isometric grip strength. Measured in kilograms [kg] (higher values = greater grip strength).
Baseline and after 3 months (post-intervention)
Plank Test
Time Frame: Baseline and after 3 months (post-intervention)
Core endurance will be assessed using the Plank Test, measuring the duration a participant can hold a plank position. A longer (seconds [s]) duration indicates better core endurance.
Baseline and after 3 months (post-intervention)
20m Sprint Test
Time Frame: Baseline and after 3 months (post-intervention)
Speed and acceleration will be assessed using the 20m Sprint Test, measuring the time taken to cover a 20-meter distance. A shorter time (seconds [s]) indicates better sprint performance.
Baseline and after 3 months (post-intervention)
Resting Heart Rate
Time Frame: Baseline and after 3 months (post-intervention)
Cardiovascular health will also be assessed by measuring resting heart rate (HR) using an electronic heart rate monitor. Lower resting heart rate (Beats per minute [bpm]) generally indicates better cardiovascular fitness.
Baseline and after 3 months (post-intervention)
Systolic Blood Pressure
Time Frame: Baseline and after 3 months (post-intervention)
Cardiovascular health will be assessed by measuring resting systolic blood pressure using an electronic blood pressure monitor. Lower values (Millimeters of mercury [mmHg]) within a normal range indicate better cardiovascular health.
Baseline and after 3 months (post-intervention)
Diastolic blood pressure
Time Frame: Baseline and after 3 months (post-intervention)
Cardiovascular health will be assessed by measuring resting diastolic blood pressure using an electronic blood pressure monitor. Lower values (millimeters of mercury [mmHg]) within a normal range indicate better cardiovascular health.
Baseline and after 3 months (post-intervention)
Body Fat Percentage
Time Frame: Baseline and after 3 months (post-intervention)
Body fat percentage will be assessed using an electronic bioimpedance tool (InBody 270) to determine the proportion of body weight composed of fat. Lower values (percentage [%]) within a healthy range indicate better body composition.
Baseline and after 3 months (post-intervention)
Skeletal Muscle Mass
Time Frame: Baseline and after 3 months (post-intervention)
Skeletal muscle mass will be assessed using an electronic bioimpedance tool (InBody 270) to measure the total mass of skeletal muscles in the body. Higher values (kilograms [kg]) indicate greater muscle mass.
Baseline and after 3 months (post-intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Dietary habits
Time Frame: Baseline and after 3 months (post-intervention)
Dietary habits will be evaluated using the SF-FFQ4PolishChildren questionnaire. This tool assesses food frequency and dietary choices in children, including the types of foods consumed, frequency of consumption, and general eating habits. Higher scores indicate more frequent consumption of a given food group. The questionnaire assesses dietary quality based on eating habits and food intake frequency.
Baseline and after 3 months (post-intervention)
Physical activity
Time Frame: Baseline and after 3 months (post-intervention)
Physical activity levels will be assessed using the Modified PAQ-C ( Modified Physical Activity Questionnaire for Children). This questionnaire gathers information on the frequency and intensity of physical activities, including sports, outdoor play, and other forms of exercise. Higher scores indicate greater levels of physical activity.
Baseline and after 3 months (post-intervention)
Programme enjoyment
Time Frame: After 3 months (post-intervention)
The enjoyment of the "11 For Health" program and football in general will be assessed through questions like "How did you like the '11 For Health' program?" and "How fun do you think football is?" Responses will be recorded on a 5-point Likert scale to measure the child's (intervention group) enjoyment and overall satisfaction with the program. Higher scores (points, [min=2, max=10]) indicate higher enjoyment level.
After 3 months (post-intervention)
Body height (BH)
Time Frame: Baseline and after 3 months (post-intervention)
Body height will be measured from the base to the vertex (top of the head) using a stadiometer to provide accurate data on the child's growth and development.
Baseline and after 3 months (post-intervention)
Body weight (BW)
Time Frame: Baseline and after 3 months (post-intervention)
Body weight will be measured using an electronic scale (InBody), providing precise data on body weight. This method is commonly used in clinical and research settings.
Baseline and after 3 months (post-intervention)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Paweł Chmura, Professor, Wroclaw University of Health and Sport Sciences

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 14, 2025

Primary Completion (Actual)

April 1, 2025

Study Completion (Actual)

September 30, 2025

Study Registration Dates

First Submitted

February 14, 2025

First Submitted That Met QC Criteria

February 19, 2025

First Posted (Actual)

February 25, 2025

Study Record Updates

Last Update Posted (Actual)

June 8, 2026

Last Update Submitted That Met QC Criteria

June 4, 2026

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • WroclawUHSS Ethics (21/2024)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The individual participant data (IPD) will only be shared in the form of published scientific articles, which will include anonymized results and analyses. Individual-level data will not be shared directly.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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