NCT07886411

Brief Summary

Anterior cruciate ligament (ACL) reconstruction is frequently associated with persistent biomechanical impairments despite clinically satisfactory recovery. The MERItest® is a standardized biomechanical assessment battery designed to evaluate movement strategies, muscle strength, and neuromuscular control during functional tasks. However, the clinical interpretation of these assessments is currently limited by the lack of normative data collected using a standardized protocol. This single-center, prospective interventional trial involving minimal risk, aims to establish a biomechanical reference database of healthy volunteers based on measurements obtained during the MERItest® assessment. The development of this normative database will enhance the interpretation of biomechanical outcomes in patients following ACL reconstruction by enabling direct comparison with a healthy reference population assessed under identical conditions.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
12mo left

Started Oct 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress2%
Oct 2026Oct 2027

First Submitted

Initial submission to the registry

October 2, 2026

Completed
13 days until next milestone

Study Start

First participant enrolled

October 15, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 21, 2026

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 15, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 15, 2027

Last Updated

October 21, 2026

Status Verified

October 1, 2026

Enrollment Period

1 year

First QC Date

October 2, 2026

Last Update Submit

October 14, 2026

Conditions

Keywords

MERITestBiomechanical reference

Outcome Measures

Primary Outcomes (1)

  • Kinematic Parameters Assessed During the MERItest®

    During running, Countermovement Jump (CMJ), bipodal drop jump, unipodal drop jump and Hop tests: Knee Flexion Excursion (°) Peak Knee Flexion (°) Foot Eversion Excursion (°) Trunk Lateral Lean (°) Contralateral Pelvic Drop (°) Hip Adduction Excursion (°) Knee Abduction Excursion (°)

    1 day

Secondary Outcomes (9)

  • Reaction Forces During Functional Tasks Assessed With the MERItest®

    1 day

  • Temporal Parameters Assessed During the MERItest®

    1 day

  • Physiological asymmetries between the lower limbs

    1 day

  • Moment Assessed During the MERItest®

    1 day

  • Impulse Assessed During the MERItest®

    1 day

  • +4 more secondary outcomes

Study Arms (1)

Healthy Volonteers

EXPERIMENTAL

Healthy volunteers will undergo the MERItest® during a single visit lasting approximately one hour. The assessment will be conducted by an experienced movement biomechanics specialist. Reflective markers (Qualisys Sports Marker Set - Functional Assessment) will then be placed on both lower limbs at the hip, knee, and ankle levels. These markers enable the collection of biomechanical data in the sagittal, frontal, and transverse planes, as well as side-to-side comparisons. Biomechanical assessment is performed using a combination of reflective markers, three-dimensional optoelectronic motion-capture cameras, and force and pressure platforms.

Other: MERITest

Interventions

Healthy volunteers will undergo the MERItest® during a single visit lasting approximately one hour. The assessment will be conducted by an experienced movement biomechanics specialist. Starting with a standardized dynamic warm-up, including walking, walking lunges, and half-squats, to prepare participants for the functional tasks and reduce injury risk. Reflective markers (Qualisys Sports Marker Set - Functional Assessment) will then be placed on both lower limbs at the hip, knee, and ankle levels. These markers enable the collection of biomechanical data in the sagittal, frontal, and transverse planes, as well as side-to-side comparisons. Biomechanical assessment is performed using a combination of reflective markers, three-dimensional optoelectronic motion-capture cameras, and force and pressure platforms.

Also known as: Biomedical evaluation
Healthy Volonteers

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Regular participation in sports activities compatible with completion of the MERItest® (at least twice per week)
  • Ability to perform all tasks included in the study protocol, including running, jumping, single-leg landings, hop tests, and strength assessments

You may not qualify if:

  • History of lower-limb surgery
  • History of anterior cruciate ligament (ACL) rupture or other major knee ligament injury
  • History of a lower-limb fracture resulting in functional impairment
  • History of symptomatic meniscal, cartilage, or tendon pathology affecting the lower limb
  • Current pain, functional limitation, or injury involving the spine, pelvis, or lower limbs
  • Any painful or traumatic event within the previous month that could affect test performance
  • History or presence of a neurological or vestibular disorder likely to impair motor control
  • Current use of medications that may affect physical or muscular performance (e.g., anti-inflammatory drugs, corticosteroids, muscle relaxants)
  • Medical contraindication to performing the exercises included in the study protocol
  • Inability to complete the entire MERItest® under standardized testing conditions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Clinique du Sport

Mérignac, 33700, France

Location

Study Officials

  • Nicolas Bouguennec, MD

    Clinique du sport

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 2, 2026

First Posted

October 21, 2026

Study Start

October 15, 2026

Primary Completion (Estimated)

October 15, 2027

Study Completion (Estimated)

October 15, 2027

Last Updated

October 21, 2026

Record last verified: 2026-10

Data Sharing

IPD Sharing
Will not share

Locations