NCT07128706

Brief Summary

This study addresses the evident gap in SRC awareness and reporting, especially at the grassroots level, by harmonizing concussion management practices across Europe and observing its impact on stakeholders' (coaches, parents, players, referees) knowledge and practices.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
7mo left

Started Jan 2024

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress81%
Jan 2024Dec 2026

Study Start

First participant enrolled

January 1, 2024

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

July 14, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

August 19, 2025

Completed
13 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2025

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Expected
Last Updated

August 19, 2025

Status Verified

July 1, 2025

Enrollment Period

1.7 years

First QC Date

July 14, 2025

Last Update Submit

August 11, 2025

Conditions

Keywords

awarenesseuropean footballyouthsports-related concussionsmanagementeducation

Outcome Measures

Primary Outcomes (1)

  • Change in Concussion Knowledge Score Pre- and Post-Educational Toolkit

    Concussion knowledge will be assessed using a structured multiple-choice questionnaire developed for this study, based on international concussion education guidelines. The same test will be administered immediately before the educational intervention (toolkit) and within 4 weeks after completion. Each correct answer is scored as 1 point. The total score ranges from 0 to 25. Higher scores indicate greater knowledge.

    Baseline (pre-intervention) and up to 4 weeks post-intervention

Secondary Outcomes (3)

  • Number of Participants Completing the Online Concussion Education Course (MOOC)

    Within 6 weeks after enrollment in the course

  • Number of Clubs Utilizing the Educational Toolkit

    Up to 3 months after intervention rollout

  • Number of Participants Attending Live Concussion Education Workshops

    Throughout the intervention period (approx. 3 months)

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Coaches, referees, parents and youth football players (up to U23) involved in football federations among Croatia, Norway, Germany and Turkey.

You may qualify if:

  • Clubs: Youth football clubs in the four countries will be invited to participate. Clubs must have:
  • The ability to implement new concussion protocols with support from the project team. This will include basic resources such as access to digital platforms (e.g., internet connectivity, devices to access training materials).
  • A willingness to engage with and integrate educational materials into their regular operations. Federations will support clubs in understanding these expectations before participation.
  • Stakeholders: Key stakeholder groups involved in youth football will be included:
  • Coaches of youth teams, regardless of prior experience in concussion management.
  • Players actively participating in youth football (targeting diverse age groups and genders).
  • Referees involved in officiating youth football matches.
  • Medical personnel, including team doctors and physiotherapists.

You may not qualify if:

  • Clubs that lack the basic resources or logistical capacity to access digital learning platforms or implement concussion protocols (as determined by federations).
  • Stakeholders who are unwilling to participate or unable to provide informed consent (or, for minors, parental/guardian consent).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Acibadem University

Istanbul, Istanbul, 34638, Turkey (Türkiye)

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 14, 2025

First Posted

August 19, 2025

Study Start

January 1, 2024

Primary Completion

September 1, 2025

Study Completion (Estimated)

December 1, 2026

Last Updated

August 19, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

data are anonymously collected

Locations