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Rate of Non-copers to Non-surgical ACL Treatment After 3 Months of Rehabilitation

Rate of Non-copers to Non-surgical ACL Treatment After 3 Months of Rehabilitation - a Prospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04847258
Enrollment
357
Registered
2021-04-19
Start date
2021-03-19
Completion date
2027-09-30
Last updated
2026-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Cruciate Ligament Injuries

Brief summary

The aim is to determine the sensitivity and specificity of a screening tool to identify patients who undergo ACL reconstruction (non-copers) after 3 months of standard rehabilitation following an anterior Cruciate ligament (ACL) injury.

Detailed description

All included patients are referred to municipal rehabilitation to resolve effusion and range of motion deficits before the first screening (baseline screening) is completed. Hereafter the patients follow 3 months municipal rehabilitation before the second screening (3 months screening). A physiotherapist performs the screening and at the second screening, this is performed prior to consulting an orthopaedic surgeon.

Interventions

OTHERStandard rehabilitation

Patients follow standard municipal rehabilitation

Sponsors

Vejle Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 49 Years
Healthy volunteers
No

Inclusion criteria

* unilateral primary ACL injury * Index injury no older than 6 months

Exclusion criteria

* Multiligament rupture * Large cartillage or meniscus injuries * Scheduled ACL reconstruction within 3 months

Design outcomes

Primary

MeasureTime frameDescription
Number of patients undergoing ACL reconstruction after 3 months of standard rehabilitation3 monthsPatients undergoing ACL reconstruction after 3 months of standard rehabilitation are defined as non-copers to the non-surgical treatment, which will define the sensitivity and specificity of the screening examination.

Countries

Denmark

Contacts

STUDY_DIRECTORClaus Varnum, ph.d.

Vejle Hosptal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 2, 2026