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Post Operative Use of Neuromuscular Electrical Stimulation (NMES) Device for ACLR Patients

University of Kansas logo

University of Kansas

Status

Not yet enrolling

Conditions

Electrotherapy
ACL Surgery
Muscle Atrophy or Weakness
ACL Injury
ACL Reconstruction

Treatments

Device: Zynex NexWave Electrotherapy Device

Study type

Interventional

Funder types

Other

Identifiers

NCT07171346
STUDY00161884

Details and patient eligibility

About

This study is being conducted to learn about how neuromuscular electrical stimulation (NMES) in addition to standard of care aids in the recovery of muscle strength in patients undergoing ACLR procedure.

Full description

The addition of neuromuscular electrical stimulation (NMES) to standard ACLR rehabilitation has been demonstrated to improve knee extension and flexion compared to standard treatment only. NMES has also shown improved lower limb loading symmetry, walking velocity, stance time, cadence, maximum voluntary isometric contraction, motor unit behavior, muscle quality, and an increase in absolute muscle strength in functional tests compared to standard care of ACLR recovery. In this study we will be comparing bi-lateral presurgical and post surgical muscle strength symmetry in patients that follow the standard ACLR rehabilitation program and patients that use the NMES in addition to standard rehab.

Enrollment

25 estimated patients

Sex

All

Ages

15 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ACLR surgical patients at KUMC sports medicine
  • 15 to 50 years old
  • BMI between 18 - 30 kg/m2
  • No limitations impacting physical function within the last 6 months (not including the ACL injury)

Exclusion criteria

  • Previous lower limb or spine injury involving surgical treatment
  • Prior spine surgery
  • Lower limb injury (other than ACL) preventing participation in physical activity for over two weeks in the past 6 months
  • Non english speaking
  • Vulnerable population, prisoner, or ward of the state

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

NMES
Experimental group
Description:
All participants will use the NMES device in addition to standard rehab protocol
Treatment:
Device: Zynex NexWave Electrotherapy Device

Trial contacts and locations

1

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Central trial contact

Clinical Research Coordinator/Supervisor - Orthopedic Surgery

Data sourced from clinicaltrials.gov

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