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Effect of Contralateral NMES on Quadriceps Activation After ACL Injury or Surgery

Does NMES Applied to the Contralateral Uninjured Side Facilitate Voluntary Quadriceps Activation Before and After ACL Surgery?

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07156734
Acronym
ACLQuadAct
Enrollment
25
Registered
2025-09-05
Start date
2025-09-30
Completion date
2026-09-30
Last updated
2025-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ACL Injury

Brief summary

A major complication after cruciate ligament injury and surgery is arthrogenic muscle inhibition of the quadriceps, which is characterised by a deficit in voluntary muscle activation in the affected leg. This can hinder rehabilitation processes, lead to impaired knee function, and negatively impact the patients' quality of life. The primary objective of this study is to assess whether voluntary quadriceps activation on the injured side is facilitated by the concomitant application of neuromuscular electrical stimulation (NMES) on the contralateral quadriceps.

Detailed description

The primary objective of this study is to assess whether injured-side voluntary quadriceps activation before and after ACL surgery is facilitated by the concomitant application of NMES on the contralateral quadriceps (uninjured side), in comparison to a control (CTRL) condition that does not involve any contralateral activity (passive rest) and to a voluntary (VOL) condition that involves a maximal voluntary contraction of the contralateral quadriceps.

Interventions

DEVICENeuromuscular Electrical Stimulation

Studies in healthy individuals have demonstrated that NMES applied to the quadriceps of one limb induces short-term increases in strength and neural drive in the contralateral homologous muscle. Since these effects have only been observed in healthy individuals, it is essential to investigate whether similar responses occur in ACL patients.

Sponsors

Schulthess Klinik
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing ACL surgery with semitendinosus tendon autograft in the Schulthess Clinic * Unilateral and primary ACL injury (with/without diagnoses of additional meniscus injury)

Exclusion criteria

* Previous surgery/ligament rupture in injured or uninjured knee or hip * Severe pain in the uninjured-side quadriceps or knee joint * Ongoing pregnancy * BMI \>30 kg/m² * Neuromuscular disease * Open wounds or tissue injuries on the anterior aspect of the thigh * Additional rupture of other knee ligaments (posterior cruciate ligament, medial collateral ligament, lateral collateral ligament) * Implanted metallic/electronic devices (cardiac pacemakers, defibrillators) * Patients getting a femoralis block (peripheral nerve block) after surgery will be excluded for the post-surgical appointment * Insufficient language comprehension

Design outcomes

Primary

MeasureTime frameDescription
EMG activityData will be collected at two time points: after ACL injury (within two weeks prior to surgery) and following ACL reconstruction (within three days post-surgery).EMG data will be recorded from the vastus medialis, vastus lateralis and rectus femoris muscles.

Contacts

Primary ContactNicola Angelo Maffiuletti, PhD
nicola.maffiuletti@kws.ch+41 44 385 75 79

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026