RecruitingNCT06235736

Do Patients With ACL Tears Demonstrate Weakness of the Soleus Muscle?

Do Patients With Anterior Cruciate Ligament (ACL) Tears Demonstrate Weakness of the Soleus Muscle?


Sponsor

University of Liverpool

Enrollment

55 participants

Start Date

Jan 17, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this prospective, cross-sectional study is to test the strength of the soleus muscle in participants who have a ACL tear confirmed by MRI. Previous studies have shown that the soleus muscle, which one of the muscles situated in the calf, decreases mechanical loading on the ACL. Therefore, we aim to test soleus muscle strength using a seated plantar flexor test. The main questions we aim to answer are: * Do patients with ACL tears demonstrate inter-limb soleus strength asymmetry (\>10%) * Do patients with ACL tears have soleus muscle weakness compared with uninjured (normative) participants? * Do changes in soleus strength values correlate with patient reported outcomes and stability, as measured by the IKDC questionnaire? To achieve this the VALD force frame will be used as the testing device for plantar flexor strength testing. This device records the force generated by the movement. This will be repeated three times on each leg as part of the testing procedure. Furthermore, as part of the testing procedure participants will be required to fill out an IKDC form to assess their knee stability. Interrater reliability of the force frame will be investigated. Further data from participants without ACL tears will be used to compare results. Thus allowing us to see if people with ACL tears have a weakness in the soleus muscle.


Eligibility

Min Age: 18 YearsMax Age: 55 Years

Inclusion Criteria4

  • ACL tear participants:
  • MRI-confirmed ACL tear.
  • Participant is willing and able to give informed consent in writing for participation in the study.
  • Male or Female, aged 18 years to 55 years of age.

Exclusion Criteria6

  • Normative values from healthy individuals:
  • No current or previous history of significant lower limb injury, or a history of previous minor injury that is symptomatic at the time of recruitment.
  • No previous lower limb surgery.
  • No course of medication, whether prescribed or over the counter, other than vitamins and mineral supplements or, for females, oral contraceptives.
  • History of chronic musculoskeletal disease or disorder in either leg that may put the participants at risk because of participation in the study including non-united fractures, epilepsy, cardiac insufficiency, severe peripheral vascular disease, aneurysms, anticoagulant therapy, recent (\<3 months) radiotherapy or chemotherapy, long term steroid use (\>3 months), pregnancy, neurological disorders (e.g., Parkinson's disease), skin conditions at point of force testing, severe osteoporosis, malignancy, rheumatoid arthritis.
  • Conditions or symptoms that may influence the result of the study, or the participant's ability to participate in the study including pain, limited range of motion, knee effusion, or anaemia.

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

Aintree Hospital, Liverpool University Hospitals NHS Foundation Trust

Liverpool, United Kingdom

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06235736


Related Trials