Actively Recruiting

Phase Not Applicable
Age: 13Years - 17Years
All Genders
ID07015541

Effects of Quadriceps Focused Interventions in Adolescents With ACL Reconstruction

Led by Stanford University · Updated on 2026-04-22

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of quadriceps-focused treatments on knee function and movement in adolescents who have undergone anterior cruciate ligament reconstruction (ACLR). The study aims to understand how these interventions impact strength and biomechanics during recovery after ACL surgery in teenagers aged 13 to 17. Participants are randomly assigned to one of two groups. One group receives a 6-week neuromuscular electrical stimulation (NMES) treatment starting the first week after surgery, followed by a 10-week blood flow restriction (BFR) intervention from weeks 7 to 16, along with standard rehabilitation care. The other group receives only the standard physical therapy care, which includes pain and swelling control, restoring knee motion, walking training, strength exercises, and running and jumping activities over 16 weeks. During the study, participants undergo evaluations including isometric knee extension force tests at 16 weeks post-surgery to measure peak force and force steadiness. Additional assessments of hip, knee, and ankle angles during jump landings are also conducted to examine movement patterns. The research includes regular monitoring and rehabilitation visits throughout the 16-week recovery period to track progress and safety.

CONDITIONS

Brief Title

Quadriceps Strengthening ACL Reconstruction

Who Can Participate

Age: 13Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • No history of knee injury or surgery on the opposite leg
Not Eligible

You will not qualify if you...

  • Bilateral knee injuries
  • Prior knee ligament injury and/or surgery
  • Multiple ligament injuries and/or ruptures
  • Conditions that prevent use of NMES and BFR treatments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 16 weeks post-surgery

Participants undergo rehabilitation after ACL reconstruction. This includes a 6-week neuromuscular electrical stimulation (NMES) intervention combined with quadriceps strengthening exercises, followed by a 10-week blood flow restriction (BFR) intervention during compound exercises. Standard physical therapy continues throughout the 16 weeks focusing on pain control, knee range of motion, gait normalization, strength training, running, and plyometrics.

Weekly visits for up to 16 weeks

Trial Site Locations

Total: 1 location

1

Stanford Medicine Children's Health

Sunnyvale, California, United States, 94087

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Low-load resistance muscular training with moderate restriction of blood flow after anterior cruciate ligament reconstruction.

Haruyasu Ohta, Hisashi Kurosawa, Hiroshi Ikeda...

https://pubmed.ncbi.nlm.nih.gov/12635796

Effects of neuromuscular electrical stimulation after anterior cruciate ligament reconstruction on quadriceps strength, function, and patient-oriented outcomes: a systematic review.

Kyung-Min Kim, Ted Croy, Jay Hertel...

https://pubmed.ncbi.nlm.nih.gov/20592480