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A Prehab Strengthening Program Prior to ACL Surgery on Lower Limb Structure and Function (ACL-Strong)

U

Université de Nantes

Status

Not yet enrolling

Conditions

ACL Injury

Treatments

Behavioral: Conventional
Behavioral: Strengthening

Study type

Interventional

Funder types

Other

Identifiers

NCT05374382
ACL-Strong

Details and patient eligibility

About

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.

Full 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).

Enrollment

75 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

75 participants in 3 patient groups

Strengthening
Experimental group
Description:
Participants received a 9-weeks strengthening-based prehabilitation program before ACL reconstruction, followed by a standardized post-operative rehabilitation program
Treatment:
Behavioral: Strengthening
Conventional
Active Comparator group
Description:
Participants received a 9-weeks conventional prehabilitation program (targeting pain knee mobility) before ACL reconstruction, followed by a standardized post-operative rehabilitation program
Treatment:
Behavioral: Conventional
Control
No Intervention group
Description:
No prehabilitation program Participants received only a standardized post-operative rehabilitation program

Trial contacts and locations

1

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Central trial contact

Antoine Nordez, PhD; Guillaume Le Sant, PhD, PT

Data sourced from clinicaltrials.gov

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