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Injury Prevention in SportsEPICNCT06748443

Enhancing Prevention of Injuries in Community Youth and Adult Amateur Football Players

A study of Injury Prevention in Sports and Adherence, run by Linkoeping University at 1 site in Sweden.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This is a type 3 hybrid cluster randomised controlled trial, where implementation of the intervention is the primary outcome and preventive effectiveness is the secondary outcome. Read more about this study

Who is it for?
Ages 10 years and olderHealthy volunteers can take part
Conditions the study is for
Injury Prevention in Sports, Adherence
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,600 participants
Where
1 siteSweden
Study dates
25 Mar 2025to Jun 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 10 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Male and female, youth and adult amateur football teams
  • Teams participating in series for players 10 years or older
  • Teams with scheduled training at least twice per week during the season
  • All eligible players in the team are invited to participate, regardless of whether they have an injury or not at study start

Who cannot join

  • Players with long-term injuries not planning to take part in match play in the 2025 season

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Martin Hägglund, Professor contact

+4613-281388

martin.hagglund@liu.se

Hanna Lindblom, PhD contact

+4613284784

hanna.lindblom@liu.se

Sweden1 site, 1 recruiting
  • Linköping university

    Linköping

    Recruiting

Other trials in Sweden

About this study

Official title: Enhancing Prevention of Injuries in Community (EPIC) Youth and Adult Amateur Football Players - Design of a Type 3 Hybrid Implementation-effectiveness Cluster Randomised Controlled Trial

This is a type 3 hybrid cluster randomised controlled trial, where implementation of the intervention is the primary outcome and preventive effectiveness is the secondary outcome.

The overall purpose of this study is to evaluate the added value of implementation support on the use and preventive effectiveness of the injury prevention exercise programme Knee Control+ in male and female, youth and adult amateur football teams.

Read more

Research questions

  1. Does use and injury preventive effect of Knee Control+ differ between teams randomised to an intervention group receiving additional support for Knee Control+ use and teams randomised to a control group with standard access to digital Knee Control+ programme material?
  2. Does coach self-efficacy to use Knee Control+, player motivation and player training dosage differ between the intervention and control groups?
  3. What are the mediators and moderators that influence use of Knee Control+?
  4. How well do the intervention and control groups adhere to Knee Control+ recommended use and is there an association between adherence and preventive efficacy?
  5. How are different components of the support material used by the intervention group teams, and how is the implementation support perceived by administrators, coaches and players in the clubs (end-users) and by fitness coaches who educate coaches about the programme (intervention deliverers)?
  6. How do coaches perceive their engagement to lead Knee Control+ training with their players and has this changed after having used the implementation support material?

Football teams will be randomised before the 2025 season to an intervention group receiving additional support for the implementation of Knee Control+ or to a control group without this support. All teams will have access to digital programme material via the Swedish Football Association.

Data on implementation of Knee Control+ and injuries (players only) will be collected weekly (coaches) and monthly (players) throughout the season using web-based questionnaires. Behavioural outcomes: for coaches self-efficacy, action and coping planning and perceived support from the club, and for players autonomous motivation, basic psychological needs and basic need support, will also be analysed.

Read the detailed description

This is a one-season study in the 2025 football season, beginning in the pre-season (March) and ending after the competitive season (November). Football coaches and players are included in the study. A sub-sample of coaches will also be included in a qualitative sub-study after the 2025 season. As part of a process evaluation, club representatives, such as club chairmen, sports directors and youth managers, will also be targeted in the same district, as well as fitness coaches delivering the interventions to the coaches. Coaches will be targeted with most of the interventions, but players and club managers will also benefit from some of the support interventions.

Fitness coaches in a nation-wide organisation (Friskis\&Svettis) will be the primary intervention-deliverers and will be educated on the Knee Control+ programme exercises and support interventions to be able to hold workshops at their venues as well as to make site visits in the teams. The research group will be responsible for the education of fitness coaches and will deliver the digital workshops to the coaches and manage the social media account.

Co-design in development of the support material has been employed. During the 2024 season, a working group with representatives for coaches and players (for practical reasons age ≥ 18) was initiated. This working group (two coaches, one former player) provided feedback and new ideas during the development of the support material and the questionnaires for coaches and players.

The workshop concept was tested three times with fitness coaches leading workshops for football coaches during the autumn of 2024 in a district not included in the main study. One site visit was also accomplished and the fitness coaches gave feedback of their experiences to the research group after this.

In the planning and execution of the study, the research group will have regular contact with representatives for football clubs, the district football associations, the Swedish football association and the fitness coach association (Friskis\&Svettis) to get their strategic input on the work being done.

Both group constellations have mainly been active during the planning for the study, but some participants may also be invited to give their view on the results and the interpretation of results after the 2025 season. After the 2025 season and potentially before upscaling of the study, the workshop strategies will be followed-up with the fitness coach association and evaluate whether any changes are needed before opening up for national dissemination.

Data will be collected primarily through web-based questionnaires covering implementation outcomes, behavioural outcomes, injury outcomes, adverse events, as well as a process evaluation.

Sample size calculations for the primary outcome were completed using the Shiny CRT online tool for binary outcomes, based on a logistic regression model. Calculations assumed 3 teams per cluster (club); a coefficient of variation equal to 0.9 was applied to account for variation in cluster sizes. An exchangeable correlation structure was assumed, and base case calculations used an intracluster correlation (ICC) of 0.02. Sensitivity analyses considered ICC values between 0.01 and 0.05. The estimated proportion of weeks where teams use the Knee Control+ in the CG is 0.5 (50%), and in the IG 0.8 (80%) based on published data. Considering a design effect (DE) of 1.04, a cluster size of 3 teams will allow for detection of a between-group difference in the primary outcome of at least 0.3 (30%) with 80% power at the 5% level of statistical significance, with total 29 clusters (85 teams). For the same difference in outcome, varying the ICC results between 0.01 and 0.05 rendered sample sizes between 28-30 clusters (83-90 teams). Therefore, the aim is to include minimum 90 teams.

For the main injury outcome, ≥7 days time-loss injuries (secondary outcome), sample size calculations were completed based on a Poisson regression model using the Shiny CRT online tool. Calculations assumed 15 players per team (cluster in the secondary analysis), a coefficient of variation equal to 0.9 was applied to account for variation in cluster sizes. An exchangeable correlation structure was assumed, and base case calculations used an intracluster correlation (ICC) of 0.02. Sensitivity analyses considered ICC values between 0.01 and 0.05. The estimated injury incidence in the CG is 0.2 (20%), and in the IG 0.1 (10%) based on published data. Considering a design effect (DE) of 1.28, a cluster size of 15 players will allow detection of a between-group relative difference in the secondary outcome of at least 0.5 (50% injury reduction) with 80% power at the 5% level of statistical significance, with total 41 teams (607 players). For the same difference in outcome, varying the ICC results between 0.01 and 0.05 rendered sample sizes between 37-54 teams (541-806 players). This equals to total 14 clusters (range 12-18 clusters) at a club level.

Data on any football related injury will be collected regardless of need of care or absence from football training or matches ("all physical complaints" injury definition).

The primary outcome, use of Knee Control+, will be analysed at team-level as the proportion of weeks with sufficient use of the programme and compared between intervention group and control group using logistic regression. The limit for sufficient training frequency is set at Knee Control+ training at least 2 times per week. Since a gradual start of injury prevention training is preferred for beginners, for players 10-12 years use of ≥3 of 6 main exercises is deemed sufficient, whereas for players >12 years, use of ≥4 of 6 main exercises is deemed sufficient to be defined as use of Knee Control+. Other measures of implementation will also be compared between groups and predominantly with parametric statistics.

Injury incidence rate (injuries per 1000 athlete exposures) and monthly prevalence rate (number of injured athletes/total number of athletes each month) will be presented with 95% confidence intervals, and incidence rate ratio and prevalence rate ratio will be calculated and compared between groups (according to intention-to-treat) using Generalized Linear Models with Poisson distribution, log link and the natural logarithm of total athlete exposures or total eligible weeks as offset denominator variables.

Qualitative interviews will be analysed using qualitative content analysis and an inductive approach.

Being tested
Support intervention for the use of Knee Control+, Information about Knee Control+
Keywords
amateur sports, injury prevention exercise programme, adherence, co-design, support for coaches

What participants receive

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

  • Support intervention for the use of Knee Control+Behavioural

    Also called Knee Control+, Injury prevention exercise programme

    Coaches will be offered a smorgasbord of support interventions that they can choose from depending on their specific needs: physical and digital workshops before and during the study, site visits to their team, digital programme material, leaflets and social media posts. Fitness coaches will be responsible for physical workshops to train the football coaches.

  • Information about Knee Control+Other

    Coaches receive information about injuries in football and the efficacy of injury prevention exercise programmes at a pre-season digital workshop, and guided to access the Knee Control+ programme from the Swedish Football Association website.

Study groups in NCT06748443
Study groupRoleWhat they receive
Intervention group receiving support for implementation of Knee Control+ExperimentalTeams in the intervention group will gain access to digital Knee Control+ programme material from the Swedish Football Association website in the pre-season and be introduced to the programme during a digital workshop prior to season start. Additionally, coaches will be offered a smorgasbord of support interventions that they can choose from depending on their specific needs: 1. physical and digital workshops aiming to increase coach self-efficacy and formalisation of action and coping plans, 2. site visits to their teams by a study designated fitness coach, aiming to increase coach self-efficacy and player autonomous motivation, 3. digital programme material with films aiming to increase coach knowledge and inspiration to use Knee Control+, 4. leaflets about Knee Control+ as inspiration and reminder to use the programme, 5. social media support as reminder to use the programme. Site visits and physical workshops will be led by specifically trained fitness coaches.
Receives: Behavioral: Support intervention for the use of Knee Control+; Other: Information about Knee Control+
Control group with standard introduction of Knee Control+Active comparatorThe control group will gain access to the same digital Knee Control+ programme material from the Swedish Football Association website in the pre-season and will be introduced to the programme during a digital workshop prior to study start.
Receives: Other: Information about Knee Control+

What is being measured

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

  1. Use of Knee Control+

    Proportion of weeks in the season with Knee Control+ training being performed at least 2 times in that week with sufficient completion of Knee Control+ components: for players 10-12 years, use of at least 3 of 6 main exercises OR for players >12 years, use of at least 4 of 6 main exercises, as reported by coaches in a web-based questionnaire on a weekly basis.

    Measured: One season, 7 months, from start of the competitive season (April 2025) to the end of the competitive season (October 2025)

Secondary outcomes (14)
  1. Adherence to Knee Control+, cumulative utilisation

    Proportion of training sessions where Knee Control+ was used, registered by coaches

    Measured: Reported weekly during the 7 months competitive season (April-October 2025)

  2. Adherence to Knee Control+, utilisation frequency

    Use of Knee Control+ n times/week

    Measured: Reported weekly (coaches) or monthly (players) during the 7 months competitive season (April-October 2025), as well as at follow-up 1 week after the season (November 2025)

  3. Adherence to Knee Control+, duration fidelity

    Minutes spent on Knee Control+ each session, reported by coaches

    Measured: Reported at follow-up 1 week after the season (November 2025)

  4. Adherence to Knee Control+, utilisation fidelity

    Assessed using questions about how Knee Control+ was used at training. Reported by coaches and players.

    Measured: Reported at follow-up 1 week after the season (November 2025)

  5. Behavioural outcomes, self-efficacy

    Change in perceived self-efficacy from baseline to follow-up. Three questions about action self-efficacy based on the Health Action Process Approach (numerical rating scale 0-10, where 0 is the least and 10 the most favorable option. Exercise self-efficacy with the Exercise Self-Efficacy Scale (9 questions, numerical rating scale 0-10, where 0 is equal to "not confident at all" and 10 is equal to "completely confident", i.e. 0 is the least and 10 is the most favourable option).

    Measured: Reported by coaches at baseline (March 2025), monthly during the 7 months competitive season (April-October 2025) and follow-up 1 week after the season (November 2025)

  6. Behavioural outcomes, presence of action plans

    One question based on the Health Action Process Approach, reported by coaches, rated on a numerical rating scale 0-10, where 0 is the least and 10 the most favourable option. Comparison of presence of action plans between groups.

    Measured: Reported at baseline (March 2025) and follow-up 1 week after the season (November 2025), as well as mid-season (August 2025).

  7. Behavioural outcomes, presence of coping plans

    One question based on the Health Action Process Approach, reported by coaches and rated on a numerical rating scale 0-10, where 0 is the least and 10 the most favourable option. Comparison of presence of coping plans between groups.

    Measured: Reported at mid-season (August 2025) and at follow-up 1 week after the season (November 2025)

  8. Behavioural outcomes, perception of club support

    Reported by coaches using the General Training Climate Scale (6 questions, Likert 1-5, where 1 is the least and 5 the most favourable option). Compared between groups.

    Measured: Reported at follow-up 1 week after the season (November 2025)

  9. Behavioural outcomes, autonomous and controlled motivation

    Change in autonomous versus controlled motivation. Reported by players with the Treatment Self-Regulation Questionnaire (4 questions focusing on autonomous motivation on a Likert 1-7, where 1 represent less and 7 more autonomous motivation, 4 questions focusing on controlled motivation on a Likert 1-7, where 1 represent less and 7 more controlled motivation).

    Measured: Reported at baseline (March 2025) and follow-up 1 week after the season (November 2025)

  10. Behavioural outcomes, basic psychological needs

    Reported by players using single-items scales (3 questions, Likert scale 1-7, where 1 is the least and 7 the most favourable option). Compared between groups.

    Measured: Reported at mid-season (August 2025) and follow-up 1 week after the season (November 2025)

  11. Behavioural outcomes, basic need support

    Reported by players using the Coaching Behavior Scale for Sport and specifically the construct covering technical skills (7 questions, Likert scale 1-7, where 1 is the least and 7 the most favourable option). Compared between groups.

    Measured: Reported at follow-up 1 week after the season (November 2025)

  12. Injury outcomes, incidence of new injuries

    Reported by players using the Oslo Sports Trauma Research Center Overuse Injury Questionnaire (OSTRC-O2, 4 questions) and additional questions to specify the injury. Injury incidence is presented separately for three severity categories:

    1. ≥7 days time-loss injuries (primary injury outcome variable is 7 day time-loss injury to the lower extremity),
    2. time-loss injuries (secondary injury outcome variable),
    3. all injuries (secondary injury outcome variable)

    Measured: Reported monthly during the 7 months competitive season (intervention period, April-October 2025).

  13. Injury outcomes, monthly prevalence of injuries

    Reported by players using the Oslo Sports Trauma Research Center Overuse Injury Questionnaire (OSTRC-O2, 4 questions) and additional questions to specify the injury. Injury prevalence is presented separately for three severity categories:

    1. ≥7 days time-loss injuries,
    2. substantial injuries (moderate or severe modifications in football participation and/or moderate or severe effects on football performance, or inability to participate in football,
    3. all injuries

    Measured: Reported monthly during the 7 months competitive season (intervention period, April-October 2025).

  14. Adverse events

    Coaches and players will report on any adverse events related to the training intervention Knee Control+. 3 bespoke questions about occurrence, frequency and type of adverse event.

    Measured: Reported at follow-up 1 week after the season (November 2025)

Timeline

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

  1. First posted27 Dec 2024
  2. Study start25 Mar 2025
  3. Primary completionNov 2025 (estimated)
  4. Study completionJun 2026 (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
Model description
Type 3 hybrid cluster randomised controlled trial
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
1,600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06748443
Sponsor's protocol ID
2024-07394-01
Acronym
EPIC
Status last verified
Apr 2025
First submitted
11 Dec 2024
Last updated
27 Apr 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified individual participant data that underlie results in publications may be available upon reasonable request to the principal investigator

Publications

  • Lindblom H, Sonesson S, Walden M, Akerlund I, Ivarsson A, Hagglund M. Enhancing Prevention of Injuries in Community youth and adult amateur football teams (EPIC) via implementation support for an exercise-based intervention: study protocol for a type 3 hybrid implementation-effectiveness cluster-randomised controlled trial. BMJ Open. 2025 Aug 26;15(8):e102008. doi: 10.1136/bmjopen-2025-102008.

    PubMed 40858379

Questions about this trial

What is this clinical trial studying?

A study of Injury Prevention in Sports and Adherence, run by Linkoeping University at 1 site in Sweden.

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 4 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: looking for participants now, as of the sponsor's last update on 27 Apr 2025. 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 Sweden. 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Martin Hägglund, Professor (+4613-281388, martin.hagglund@liu.se), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Use of Knee Control+ (time frame: One season, 7 months, from start of the competitive season (April 2025) to the end of the competitive season (October 2025)). 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 NCT06748443, 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 27 Apr 2025.

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