Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
NCT07128602

Determining the Effects of Non-invasive Brain Stimulation to Improve Quadriceps Muscle Function After ACL Reconstruction

Led by Arcadia University · Updated on 2026-05-07

42

Participants Needed

1

Research Sites

142 weeks

Total Duration

On this page

Sponsors

A

Arcadia University

Lead Sponsor

E

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

After knee surgery for a torn ACL, many women struggle with weak thigh muscles for years, partly due to reduced brain signals to these muscles. Our research tests a new approach to improve recovery by using low-level brain stimulation to boost these signals. The investigators will study 42 women, aged 18-35, who had ACL surgery. They'll be split into two groups: one receiving real brain stimulation and another getting a placebo, both during thigh-strengthening exercises. Over six sessions, the investigators measure thigh muscle strength, speed, and steadiness, plus two brain signal measures, using special equipment. The investigators will also check if stronger brain signals lead to better muscle performance, especially in women. Our goal is to show that this new method strengthens thigh muscles better than standard rehab, helping women recover better after surgery. If successful, this could improve physical therapy for women recovering from ACL surgery, making daily activities and return to sport easier.

CONDITIONS

Official Title

Determining the Effects of Non-invasive Brain Stimulation to Improve Quadriceps Muscle Function After ACL Reconstruction

Who Can Participate

Age: 18Years - 35Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female participants 2 to 6 months after ACL reconstruction surgery
Not Eligible

You will not qualify if you...

  • Multiple ligament reconstruction
  • Osteochondral procedures
  • Any previous lower extremity surgery
  • Previous ACL injury
  • Metal or implants in the head or neck
  • History of neurological disease
  • Seizures
  • Severe migraines
  • Concussion within the last 6 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ryan Zarzycki

Glenside, Pennsylvania, United States, 19038

Actively Recruiting

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Research Team

R

Ryan Zarzycki, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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