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Primary PreventionNCT06180772

FIT FIRST FOR ALL - The Dose-Response Study

A study testing FIT FIRST in people with Primary Prevention, run by University of Southern Denmark at 1 site in Denmark.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

In the present study, FIT FIRST 10 will run over 20 weeks, with cardiometabolic fitness as the primary outcome and project acceptability as the co-primary outcome. In this study the investigators will be testing the dose-response of the FIT FIRST concept by having two experimental groups. Read more about this study

Who is it for?
Ages 6 to 11 yearsHealthy volunteers can take part
Conditions the study is for
Primary Prevention
What is being tested?
FIT FIRST
Could I receive a placebo?
No, everyone receives an active treatment
How many people
2,400 participants
Where
1 siteDenmark
Study dates
10 Dec 2022to 24 Dec 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 11 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • part of enrolled classes

Who cannot join

  • none

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • University of Southern Denmark

    Odense, 5000

Other trials in Denmark

About this study

In the present study, FIT FIRST 10 will run over 20 weeks, with cardiometabolic fitness as the primary outcome and project acceptability as the co-primary outcome. In this study the investigators will be testing the dose-response of the FIT FIRST concept by having two experimental groups. This will be a cluster RCT with a 1:1:1 recruitment of control schools, intervention schools with 3 weekly 40-min FIT FIRST 10 lessons, and intervention schools with 1.5 weekly 40-min session. There will be recruited a total of 1000 children, with 500 8-9-year-olds from 2nd and 3rd grade in each group from a minimum of 40 classes from 16 schools. There will be subgroup analyses of children with low socioeconomic status and ethnic minority background. Intervention effects will be tested as on health profile, cardiometabolic and musculoskeletal fitness, motivation for physical activity, acceptability of the programme for stakeholders as well as the implementation potential. The study will be running in Q1 and Q2 in 2023.

It is hypothesized that the FIT FIRST 10 concept will improve the well-being, increase sports club participation as well as increase fitness and health levels among 8-9-year-old children with low fitness, low socioeconomic and/or ethnic minority background. However, it is also hypothesized that the effects on well-being and fitness levels caused by the intervention may be most significant among ethnic minority children not enrolled in sports clubs.

Read the detailed description

Background Physical activity (PA) is an important part of a healthy lifestyle for children and youth, as it improves physical fitness, motor competences and well-being, and reduces the risk of developing overweight and lifestyle diseases later in life. Current recommendations from the Danish Health Authorities are that young people should participate in at least 60 min of moderate-to-vigorous physical activity (MVPA) per day, of which at least 3 times 30 min per week should involve vigorous physical activity (VPA).

As children's total amount of daily PA is a product of their activities in and outside of school, it can be of value to look for synergetic effects that can be achieved by having developed abilities and motivation for activities in school that can be used in leisure time sports clubs.

Based on the beforementioned knowledge, investigators have developed the FIT FIRST programme. FIT FIRST was originally an acronym for a 40-week intervention study for 8-9-year-olds: Frequent Intense Training through Football, Interval Running and Circuit Strength Training. This study showed that 3x40 min per week of FIT FIRST ball game and circuit strength training activities was very effective in improving fat percentage, blood pressure, muscle strength, postural balance and bone mineralization. In 2018, the FIT FIRST 10 concept was developed for 6-9-year-olds that covered 10 sports using the same principles.

In the present study, FIT FIRST 10 will run over 20 weeks with cardiometabolic and musculoskeletal fitness as the primary outcomes and project acceptability as co-primary outcomes. In this study the investigators will be testing the dose-response of the FIT FIRST 10 concept by having two experimental groups. This will be a cluster RCT with a 1:1:1 recruitment of control schools, intervention schools with 3 weekly 40-min FIT FIRST 10 lessons, and intervention schools with 1.5 weekly 40-min session. There will be recruited a total of 2400 children, with 800 8-9-year-olds from 2nd and 3rd grade in each group from approximately 60 classes from 24 schools. There will be subgroup analyses of children with low socioeconomic status and ethnic minority background.

Intervention effects will be tested as in Study I on health profile, cardiometabolic and muscular fitness, motivation for physical activity, acceptability of the programme for stakeholders, and implementation potential. The study will be running in Q1 and Q2 in 2023.

Measures:

Fitness levels and health profile:

Yo-Yo IR1 Children's test (total distance in meters) will be used to evaluate cardiometabolic fitness. For muscular fitness, the standing long jump test (in meters), the handgrip strength test (in kilograms), the arrowhead agility-test (in seconds) and the stork balance stand test (in seconds) will be used.

To evaluate the effects on health, measurements of resting heart rate (beats per minute) and blood pressure (millimeters of mercury) will be recorded.

Also, the participants' body composition and height will be measured using Tanita scales and InBody 230 Bioimpedance. The measurements of the participants' body composition includes measures of their body mass (in kilograms), skeletal muscle mass (in kilograms) and fat percentage. To investigate the prevalence of overweight and obesity, BMI z-scores (kg/m^2) will be calculated by using the participants' relative weight adjusted for child age and sex.

Well-being, body image, self-worth and quality of life:

KIDSCREEN 27, which is a validated questionnaire measuring physical well-being, mental well-being, social well-being and school well-being in the school environment will be used. Children's body perception and satisfaction will be measured using the Children's Body Image Scale, a pictorial scale developed for 7-11 year old children. Furthermore, the short form of the Physical Self-Inventory (PSI-S) will be used to evaluate overall selfworth (i.e., perceptions of one's physical self) and specific sub-components (physical appearance, strength, physical condition and sport competence).

Evaluation of physical activity and sport club participation:

A questionnaire will provide information in terms of types of activities undertaken outside school.

Process evaluation:

The RE-AIM framework will be used to ensure a holistic assessment of intervention and implementation outcomes. A mixed-method approach, including document analysis, participant observations, objective measurements, survey instruments and interviews will be applied. The RE-AIM framework has been used extensively to assess school-based PA interventions and to guide process evaluations. The RE-AIM have been in several studies. The framework constitutes five key elements, i.e. Reach, Effectiveness, Adoption, Implementation and Maintenance.

Also, the ecological model of implementation, by Durlak and Dupree will be used.

Being tested
FIT FIRST

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • FIT FIRSTBehavioural

    High intensity sports drills and games

Study groups in NCT06180772
Study groupRoleWhat they receive
ControlNo interventionContinue normal activities
3/wkExperimentalUse FIT FIRST 3 times pr. week
Receives: Behavioral: FIT FIRST
1.5/wkExperimentalUse FIT FIRST 1.5 times pr. week
Receives: Behavioral: FIT FIRST

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cardiometabolic fitness as assessed by the achieved distance in the Yo-Yo IR1 Children's test

    Cardiometabolic fitness profile will be evaluated by using the Yo-Yo IR1 Children's test measured as the total distance in meters as an indicator for the participants' ability to perform intermittent exercise and their cardiometabolic fitness. The longer the distance, the better the cardiometabolic fitness of the participants.

    Measured: Change from baseline to week 20

  2. Project acceptability as assessed by observations and teachers questionnaires

    Observations will describe the acceptability and specific teacher questionnaires will be applied to evaluate the acceptability of the project.

    Measured: Change from baseline to week 20

Secondary outcomes (9)
  1. Muscle strength of the lower body as assessed by the standing long jump performance

    For muscular strength of the lower body, the standing long jump test will be used. The outcome will be the jumped distance measured in meters. The standing long jump test is applied to asses the lower body strength of the participants and the higher the score, the better the performance. The participants have to attempts.

    Measured: Change from baseline to week 20

  2. Well-being as assessed by the questionnaires KIDSCREEN 27

    To evaluate the participants' well-being, - KIDSCREEN 27

    Measured: Change from baseline to week 20

  3. Fat percentage based on bioimpedance.

    To evaluate the effects on Fat percentage, bioimpendance will be used

    Measured: Change from baseline to week 20

  4. Postural balance as assessed by the stork balance stand test

    The stork balance stand test, measured three times on each leg, will be used to evaluate the participants' ability to maintain a state of balance in a static position. The outcome is measured in seconds and a higher score indicates a better outcome.

    Measured: Change from baseline to week 20

  5. Agility as assessed by the arrowhead agility-test

    The arrowhead-agility test is applied to assess the agility of the participants, their body control and change of direction. In this test, the participants have to attempts and will be running to the right side in both attempts. The outcome is measured in seconds. A lower score indicates a better outcome.

    Measured: Change from baseline to week 20

  6. General strength as assessed by the handgrip strength test

    The handgrip strength test is used to asses the participants' general strength level, measured in kilograms. A higher score indicates a better general strength. The participants have to attempts and use their dominant arm.

    Measured: Change from baseline to week 20

  7. Health profile as assessed by resting heart rate

    To evaluate the effects on health, measurements of resting heart rate (beats per minute).

    Measured: Change from baseline to week 20

  8. Muscle mass

    To evaluate the effects on Muscle mass, bioimpendance will be used.

    Measured: Change from baseline to week 20

  9. systolic and diastolic blood pressure

    systolic as well as diastolic blood pressure (millimeters of mercury) will be recorded three times with an automatic BP-monitor (M6 HEM-7322U-E; Omron, Hoofddorp, The Netherlands).

    Measured: Change from baseline to week 20

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Dec 2023
  2. Study start10 Dec 2022
  3. Primary completion24 Dec 2024 (estimated)
  4. Study completion24 Dec 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
2,400 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06180772
Sponsor's protocol ID
USouthernDenmark-FIT FIRST
Status last verified
Dec 2023
First submitted
12 Dec 2022
Last updated
22 Dec 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Eckert C, Thogersen-Ntoumani C, Larsen MN, Koch S, Christiansen LB, Meiner CB, Cimenti C, Tarantino G, Ntoumanis N, Krustrup P. Dose-Response Effects of a 4-Month FIT FIRST 10 School-Based Multisport Programme on Physical Fitness and Psychosocial Well-Being in Children Aged 7-11: A Three-Arm Cluster-Randomized Controlled Trial. Scand J Med Sci Sports. 2026 Jun;36(6):e70311. doi: 10.1111/sms.70311.

    PubMed 42184096

Questions about this trial

What is this clinical trial studying?

A study testing FIT FIRST in people with Primary Prevention, run by University of Southern Denmark at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 22 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cardiometabolic fitness as assessed by the achieved distance in the Yo-Yo IR1 Children's test (time frame: Change from baseline to week 20). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06180772, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Dec 2023.

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