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Completed

NCT Number: NCT07448064

Eccentric Phase Biomechanics of the Countermovement Jump After Anterior Cruciate Ligament Reconstruction

Purpose: This study aims to better understand how force is produced during a vertical jump in individuals approximately six months after anterior cruciate ligament reconstruction compared with healthy individuals. After this type of knee surgery, many patients recover well clinically but may still present strength differences between the operated and non-operated leg. These differences are not always visible during routine clinical testing but may influence performance and potentially increase the risk of reinjury. By analyzing how force is generated during a standardized countermovement jump, this study seeks to identify whether biomechanical alterations persist at this stage of recovery and to improve decision-making related to rehabilitation and return to sport.

Study Design: This is an observational comparative study. Participants who have undergone anterior cruciate ligament reconstruction using a hamstring tendon graft will be assessed between five and seven months after surgery. Their results will be compared with those of healthy recreationally active individuals without a history of recent knee injury. No experimental treatment or modification of rehabilitation will be introduced as part of this study.

Procedures: Participants will complete a brief standardized warm-up followed by three maximal vertical countermovement jumps performed on a force platform. During the test, participants will keep their hands on their hips and will be instructed to jump as quickly and as high as possible. The force platform measures ground reaction forces from each leg separately, allowing detailed analysis of the lowering phase (when the body bends before jumping) and the push-off phase (when the body propels upward). The entire testing session lasts only a few minutes and reflects movements commonly used in rehabilitation and sports settings.

Measurements: The primary measurements include jump height and the mean force produced by each leg during both the eccentric (lowering) and concentric (push-off) phases of the jump. The study will also calculate limb symmetry indices to determine the degree of difference between the operated and non-operated legs. These measurements provide objective information about neuromuscular recovery and functional performance after surgery.

Risks: The procedures involve physical activity comparable to exercises already performed during standard rehabilitation. The risks are minimal and similar to those encountered during routine physical training. Participants may stop the test at any time if they experience discomfort.

Potential Benefits: Participants may not receive direct personal benefit from taking part in the study. However, the results may contribute to improving rehabilitation strategies, refining criteria used for return-to-sport decisions, and enhancing long-term functional outcomes after anterior cruciate ligament reconstruction. A better understanding of persistent biomechanical alterations may ultimately help reduce the risk of secondary injury and optimize recovery pathways.

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Haute Ecole ARC

Delémont, Switzerland

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Post-Anterior Cruciate Ligament Reconstruction Cohort:

Age between 18 and 40 years

Primary anterior cruciate ligament reconstruction using a hamstring tendon autograft

Assessment performed between 5 and 7 months post-surgery

Completion of standard postoperative rehabilitation

Medical clearance for functional testing

Ability to perform maximal effort jumping and strength testing

Healthy Control Cohort:

Age between 18 and 40 years

Recreationally active (minimum two sessions of physical activity per week)

No history of anterior cruciate ligament injury

No lower limb surgery

No lower extremity injury within the past 12 months

No current knee pain or functional limitation

Exclusion criteria

  • Previous anterior cruciate ligament reconstruction on either knee (except the index surgery for the ACL group)

Concomitant ligament reconstruction (e.g., posterior cruciate ligament, medial collateral ligament, lateral collateral ligament)

Symptomatic meniscal repair limiting full participation in testing

Neurological disorders affecting lower limb function

Inflammatory joint disease

Pregnancy

Inability to perform maximal effort testing

Treatment and study plan

Countermovement Jump Force Platform Assessment

Other

Participants perform three maximal countermovement jumps on a calibrated force platform after a standardized warm-up. Hands are kept on the hips during testing. The platform records ground reaction forces from each limb separately during the eccentric (lowering) and concentric (push-off) phases of the jump. Jump height and limb symmetry indices are calculated. This procedure is used for biomechanical and functional assessment only and does not modify standard rehabilitation.

isokinetic test

Other

isokinetic dynamometry is performed to assess concentric quadriceps and hamstring strength at standardized angular velocities. Peak torque values and limb symmetry indices are calculated for quadriceps and hamstring

Primary outcomes

  1. Eccentric Mean Force

    Time frame: 3 and 6 months

Secondary outcomes

  1. Concentric Mean Force

    Time frame: 3 and 6 months

  2. Jump Height

    Time frame: 3 and 6 months

  3. Quadriceps and Hamstring Peak Torque

    Time frame: 3 and 6 months

Sponsors and collaborators

Lead sponsor

Haute Ecole ARC Sante

Other

Registry information

Official study title

Analysis of Biomechanical Alterations During the Eccentric Phase of the Countermovement Jump in Patients After Anterior Cruciate Ligament Reconstruction

Acronym: DECAL

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Mar 4, 2026
Registry last updated
Mar 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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