- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06910085
Kettlebell-classroom Training (kettleclass)
Kettlebell-classroom: Feasibility and Effect of a Daily Dose of Resistance Training in Primary School Children - a Control\ed Trial
Physical fitness is a crucial health marker, predicting both cardiovascular and all-cause mortality. Muscular strength, an essential component of physical fitness, underpins physical and psychological well-being, particularly from childhood. Increasing sedentary behavior has led to rising obesity and cardiovascular disease rates in children, exacerbated by the COVID-19 pandemic and the emergence of pediatric dynapenia. Muscular fitness positively affects body composition, bone health, psychological health, and academic performance, and is necessary for fundamental motor skills.
In Basel, a ten-year trend shows declining physical fitness and rising obesity among primary school children, especially those from lower socio-economic backgrounds with less access to sports. This presents an opportunity to promote physical activity in schools. The "Kettlebell Classroom" project aims to introduce daily, playful resistance training with kettlebells over seven weeks in various schools, focusing on culturally and socially less integrated children.
Evidence supports the benefits of resistance training (RT) for children, including increased joint stability, improved motor skills, reduced injury risks, and increased spontaneous physical activity. Despite WHO recommendations for muscle and bone-strengthening activities three times a week, these guidelines are often unmet. This project aims to demonstrate the effectiveness of short, intensive exercise sessions for children, with the goal of expanding the initiative across Basel to improve health outcomes for all children.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Basellandschaft
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Basel, Basellandschaft, Switzerland, 4052
- Department of Sport, Exercise and Health
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- all of the selected second-graders who can participate in physical education lessons will be included in the study
Exclusion Criteria:
- Children with a medical certificate, that prohibits physical activity, will be excluded from performance testing and training intervention.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: kettlebell training
The intervention involves daily, supervised resistance training sessions for primary school children, integrated directly into the classroom setting. Over a period of 7 weeks, participating second-grade school classes perform 15-minute kettlebell-based workouts every school day, totaling 35 sessions. The sessions are designed to be: Playful and age-appropriate Focused on whole-body strength and motor skill development Based on functional, multi-joint movements using bodyweight and kettlebells Adaptable to individual ability levels Including elements of teamwork and cooperation to enhance motivation and enjoyment The goal is to improve muscular strength, coordination, fitness, and psychosocial well-being, particularly in children from lower socio-economic backgrounds. |
15 min of body weight or kettlebell loaded strength training
|
|
No Intervention: regular schedule - control
The control group consists of parallel second-grade school classes that do not receive any active intervention during the study period. These students continue with their regular school routine and standard physical education classes, without the additional kettlebell training sessions. Like the intervention group, they: Undergo the same pre- and post-intervention test battery assessing strength, coordination, fitness, and anthropometric measures Are assessed during school hours using identical equipment and protocols Serve as a baseline comparator to evaluate the effectiveness and feasibility of the resistance training intervention |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximal strength
Time Frame: seven week intervention
|
The mid-thigh pull is measured on the force plate, as is the hand grip force (Leonardo Mechanograph® Novotec Medical GmbH, Pforzheim, Germany).
The mid-thigh pull corresponds to a static deadlift, i.e. pulling up a bar in the centre of the thigh, and thus provides an image of the force transmission of the muscle loops up to the hand force to transfer the force to the measuring device.
The test subject has a hip and knee angle of 135-140° and tries to pull as quickly and strongly as possible on the vertically fixed bar in the centre of the thigh.
As the test subject is standing on the force plate, the transmitted force is measured precisely.
In contrast to the dynamic 1-repetition maximum, this simple test offers a high level of safety as an isometric measurement and, in particular, has a high test-retest reliability.
This measurement is therefore not only attractive to perform, but also makes it easy to analyse strength curves and maximum strength.
|
seven week intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Handgrip strength
Time Frame: seven week intervention
|
The handgrip force is measured using a size-adjustable application to take into account the span of the respective hand size.
The measurement is performed with the arm extended vertically and provides a safe and reliable measurement for children.
|
seven week intervention
|
|
sprint performance
Time Frame: seven week intervention
|
20 m Sprint: Electronic measurement of a timed (seconds) 20 m sprint, starting from a resting position.
Start follows after an acoustic signal, with a precision of 1/100 second.
|
seven week intervention
|
|
jump performance
Time Frame: seven week intervention
|
Countermovement jump: Power per body mass, determined from a vertical countermovement jump (CMJ), has been shown to be correlated to leg extension strength in children while representing a more natural movement.
The CMJ will be performed on a force plate (Leonardo Mechanograph®, Novotec medical, Pforzheim, Germany) with arms akimbo.
The instruction will be to jump as high as possible.
After familiarization, each participant performs 2-5 trials, with the best of the two trials with <5% difference being used for the analysis.
The most important outcome parameter of this test is the maximum power output (peak power) normalized to body weight.
The CMJ had a high intra-trial reproducibility (ICC>0.95) in 6-8 year old children, whereas inter-session variation has been reported to be high in children aged 6-12 years as well (ICC=0.95,
SEE=1.92 standard error of estimate).
|
seven week intervention
|
|
shuttle-run performance
Time Frame: seven week intervention
|
20 m Shuttle-Run-test: This is a validated test which measures aerobic capacity by running forth and back for 20 m, with an initial running pace of 8.0 km/h and a progressive 0.5 km/every minute raise of the running speed given by a sound.
The maximal performance will be reached when the child does not cross the 20 m line at the moment of the beep for two consecutive 20 m distances.
Number of "paliers" (1 palier≅1 minute) performed will be counted with a precision of 0.5 paliers.
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seven week intervention
|
|
balance performance
Time Frame: seven week intervention
|
This test of coordination includes balancing backward on 3 m long bars with a width of 3, 4.5, and 6 cm, respectively.
The number of steps until the child's foot touches the floor will be counted; 3 trials will be performed for each bar width.
The sum of these 9 tests will be used for statistical analysis.
|
seven week intervention
|
|
object control
Time Frame: seven week intervention
|
The Eye-Hand-Control test is valid and reliable and determines the level of controlling an object (tennis ball) while conducting repetitive movements (i.e., left-hand throw, right-hand catch, or right-hand throw, and left-hand catch, etc.) as frequently as possible in a time-constrained task of 30 sec.
The children are free to use overhand and/or underhand techniques or a combination of both for throwing and catching.
Children had to stand 1 m from a wall and throw the tennis ball at eye level on a wall.
Participants conducted this test twice, with the number of successful ball catches across both trials resulting in the test score.
|
seven week intervention
|
|
blood pressure, body composition
Time Frame: seven week intervention
|
Anthropometry and blood pressure will be analysed on a seperate day, in a separate room parallel to the usual school lessons.
3 students will be evaluated at the same time.
|
seven week intervention
|
|
side hop
Time Frame: seven week intervention
|
Jumping sidewards: Measurement for speed and coordination.
Jumping with both legs together on alternating sides of a bunton of wood, as many times as possible, within 15 seconds.
Two trials will be performed.
The number of jumps will be counted.
The sum of the number of jumps of the two tests will be used for statistical analysis.
|
seven week intervention
|
Collaborators and Investigators
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
- 2024-01074 (Other Identifier: ethics committee)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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