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Enrolling by invitation NCT05752695

Operation Korsband

Observational Anterior Cruciate Ligament Injuries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Anterior Cruciate Ligament Injuries. Basic parameters: 12 years — 55 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Sweden
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Risk Factors for Cruciate Ligament Injuries

Overview

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.

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.

Primary outcome measures

  • Total work load [Time frame: Day 1]
Secondary outcome measures (7)
  • Number of teams [Time frame: Day 1]
  • Injury situation 1 [Time frame: Day 1]
  • Injury situation 2 [Time frame: Day 1]
  • Injury situation 3 [Time frame: Day 1]
  • Physical well-being [Time frame: Day 1]
  • Mental wellbeing [Time frame: Day 1]
  • Previous injury [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • Athlete
  • Defined ACL injury

Exclusion criteria

  • Non athletes
  • Younger than 12 years

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Sweden · 1 center
  • Sofia Ryman Augustsson — Kalmar

Identifiers

NCT: NCT05752695 · 2022-06554-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗