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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05374382
Other study ID # ACL-Strong
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2022
Est. completion date September 2024

Study information

Verified date May 2022
Source Université de Nantes
Contact Guillaume Le Sant, PhD, PT
Phone +251837234
Email guillaume.le-sant@univ-nantes.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Atrophy and weakness are ubiquitous after a ACL rupture and associated with a worsened long-term recovery of individual capacities, despite surgery and rehabilitation. Preoperative rehabilitation (prehab) is believed to prepare patients for surgery and post-operative rehabilitation. However, prehab programs are highly variable, and do not always aim to develop/maintain neuromuscular parameters. The purpose of this study is to assess the effects of a lower limb strengthening training program during prehab prior to ACL Surgery on lower limb structure and function.


Description:

Recruited participants will be randomly allocated to one of the three groups of participants constituted in this study. The two first groups will receive prehabilitation prior to ACL reconstruction (differing in program type). All participants will receive standardized post-surgery rehabilitation (based on international recommandations).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 75
Est. completion date September 2024
Est. primary completion date September 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - age : 18 to 55 - first episode of ACL injury - having a planed ACL reconstruction - volunteer to participate Exclusion Criteria: - age : <18 or >55 - previous episode of ACL injury/reconstruction - no ACL reconstruction

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Strengthening
3x/w, 9 wks supervised strengthening program, during prehabilitation to ACL surgery
Conventional
Participants received a 9-weeks conventional prehabilitation program (targeting pain knee mobility) before ACL reconstruction, followed by a standardized post-operative rehabilitation program

Locations

Country Name City State
France Université de Nantes - MIP UR 4334 (Motricity, Movement, Interactions) Nantes

Sponsors (1)

Lead Sponsor Collaborator
Université de Nantes

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in muscle strength of the knee muscles Maximal muscle strength of knee flexors/extensors will be assessed using isokinetic dynamometer, and extension and flexion torques during a maximum voluntary contraction (MVC).
Unit : Newton meter (Nm)
week 0 (baseline); week 9 (post-intervention, short term) ; 6 months after the surgery (post-intervention, mid-term) and 12 months after the surgery (post-intervention, long-term)
Primary Change in muscle volume of the knee muscles Muscle volume of the knee muscles (hamstring and quadriceps) will be assessed using 3D ultrasound imaging, at rest in a prone (hamstring) or supined (quadriceps) position.
Unit : millimeters (mL)
week 0 (baseline); week 9 (post-intervention, short term) ; 6 months after the surgery (post-intervention, mid-term) and 12 months after the surgery (post-intervention, long-term)
Primary Change in the stiffness of knee muscles An index of muscle stiffness will be assessed via the shear modulus using ultrasound shear wave elastography, at rest in a prone (hamstring) or supined (quadriceps) position.
Unit : kiloPascals (kPa)
week 0 (baseline); week 9 (post-intervention, short term) ; 6 months after the surgery (post-intervention, mid-term) and 12 months after the surgery (post-intervention, long-term)
Primary Change in lower limb function Single leg hop test. Participants will be instructed to jump as far as possible on a single leg, without losing balance and landing firmly. The distance is measured from the start line to the heel of the landing leg.
Unit : centimeters (cm)
week 0 (baseline); week 9 (post-intervention, short term) ; 6 months after the surgery (post-intervention, mid-term) and 12 months after the surgery (post-intervention, long-term)
Primary Change in patient's opinion about the knee and associated problems Patient's self-related opinion about symptoms and activity will be assessed using the International Knee Documentation Committee Subjective Knee Form (IKDC).The IKDC is consisted of 10 questions.
Unit : score, scaled between 0 (=bad) and 100 (= good function)
week 0 (baseline); week 9 (post-intervention, short term) ; 6 months after the surgery (post-intervention, mid-term) and 12 months after the surgery (post-intervention, long-term)
Primary Change in patient's opinion to return to sport Patient's self-related opinion out the impact of returning to sport will be assessed using the Anterior Cruciate Ligament - Return to Sport after Injury (ACL-RSI) questionnaire.
The ACL-RSI consists of 12 questions. Unit : score, scaled between 0 (=bad) and 100 (= more psychologically ready to return to sport)
week 0 (baseline); week 9 (post-intervention, short term) ; 6 months after the surgery (post-intervention, mid-term) and 12 months after the surgery (post-intervention, long-term)
Secondary Health consumption Drugs intakes, dates of physiotherapy/medical consultations, date of return to work will be assessed through a diary
Unit : self-reported date, in a paper diary
week 0 (baseline); week 9 (post-intervention, short term) ; 6 months after the surgery (post-intervention, mid-term) and 12 months after the surgery (post-intervention, long-term)
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