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Anterior Cruciate Ligament InjuriesNCT05752695

Operation Korsband

An observational study of Anterior Cruciate Ligament Injuries, run by Linnaeus University at 1 site in Sweden.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

This study aims to investigate if a detailed and comprehensive survey can identify, explain and prevent the risk factors for ACL injury. A a new questionnaire has been developed with questions to young athletes who have suffered an anterior cruciate ligament injury. Read more about this study

Who is it for?
Ages 12 to 55 years
Conditions the study is for
Anterior Cruciate Ligament Injuries
How many people
200 participants
Where
1 siteSweden
Study dates
1 Sep 2023to 31 Dec 2028
How long will I take part?
1 Day
Phase
Observational
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 12 to 55 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Study population: Athletes with ACL defined ACL injury.

Who may be able to join

  • Athlete
  • Defined ACL injury

Who cannot join

  • Non athletes
  • Younger than 12 years

Trial locations and contacts

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

Sweden1 site
  • Sofia Ryman Augustsson

    Kalmar, 391 82

Other trials in Sweden

About this study

Official title: Risk Factors for Cruciate Ligament Injuries

This study aims to investigate if a detailed and comprehensive survey can identify, explain and prevent the risk factors for ACL injury.

A a new questionnaire has been developed with questions to young athletes who have suffered an anterior cruciate ligament injury. The questionnaire is more detailed and provide more information about how the anterior cruciate ligament injury occurred compared with the questionnaires currently available in the literature. This careful documentation will provide new knowledge and might be used to identify, explain and prevent risk factors that cause young athletes to suffer an anterior cruciate ligament injury.

Read the detailed description

Participants will be prospectively recruited at their first physiotherapist clinical session. On this occasion, participants will be asked to fill in a questionnaire regarding injury situation, game or training, sex, age, sport affiliation, level of sport, other aspects of sport such as participation in several teams and junior versus senior games/training. In addition, questions regarding previous injury will also be documented.

Medical subject headings
Anterior Cruciate Ligament Injuries

What participants receive

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

Study groups in NCT05752695
Study groupRoleWhat they receive
ACL injured athletesAthletes with defined ACL injury.

What is being measured

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

  1. Total work load

    Total hours, per week, of practice and games.

    Measured: Day 1

Secondary outcomes (7)
  1. Number of teams

    In team athletes, the number of teams in which the athlete participates.

    Measured: Day 1

  2. Injury situation 1

    Question regarding when the injury occurred; training vs game.

    Measured: Day 1

  3. Injury situation 2

    Question regarding at what situation the injury occurred (e.g. jump, landing, header duel, defense, attack...)

    Measured: Day 1

  4. Injury situation 3

    Question regarding at what time, during a game, the injury occurred; approximate match minute

    Measured: Day 1

  5. Physical well-being

    Physical well-being is assessed with a likert scale ranging from 1-5 where '1' represents 'out of shape' while '5' represents that you felt 'in top shape'.

    Measured: Day 1

  6. Mental wellbeing

    Mental well-being is assessed with a likert scale ranging from 1-5 where '1' represents 'out of shape' while '5' represents that you felt 'in top shape'.

    Measured: Day 1

  7. Previous injury

    Description of previous injury prior to the ACL injury, such as other injuries to lower extremity or concussion.

    Measured: Day 1

Timeline

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

  1. First posted3 Mar 2023
  2. Study start1 Sep 2023
  3. Primary completion31 Dec 2028 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Case only
Time perspective
Cross-sectional
Enrolment
200 participants (estimated)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT05752695
Sponsor's protocol ID
2022-06554-01
Status last verified
Dec 2025
First submitted
21 Feb 2023
Last updated
30 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Anterior Cruciate Ligament Injuries, run by Linnaeus 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 2 inclusion and 2 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: enrolling by invitation, as of the sponsor's last update on 30 Dec 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?

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?

Total work load (time frame: Day 1). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 30 Dec 2025.

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