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

Part of paid clinical trials in Kansas City, Kansas.

Sponsor
University of Kansas Medical Center
Study ID
NCT07171346
Status
Enrolling By Invitation

Conditions

  • ACL Injury
  • ACL Reconstruction
  • ACL Surgery
  • Electrotherapy
  • Muscle Atrophy or Weakness

Eligibility Criteria

Sex
ALL
Age
15 Years - 50 Years
Healthy Volunteers
Not accepted

Interventions

  • Zynex NexWave Electrotherapy Device — DEVICE
    All participants will use the NMES device in addition to standard rehabilitation

Study Details

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.

Key Dates

Start date
Feb 10, 2026
Status verified
Mar 2026
Primary completion
Nov 30, 2027
Completion
Jun 30, 2028

Study Design

Enrollment
25 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: NMES
    All participants will use the NMES device in addition to standard rehab protocol

Primary Outcome Measure

Bilateral Muscle Symmetry Index [ Time Frame: pre-operative to 3 months post-op ]

Locations (1)

FacilityCityStateZIPSite coordinators
University of Kansas Medical CenterKansas CityKansas66160-

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University of Kansas Medical Center· Kansas City, KS

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