Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03273673 · ClinicalTrials.gov registry record · NA

Reduction of Risk Factors for ACL Re-injuries Using a Novel Biofeedback Approach

A NA study, sponsored by Virginia Polytechnic Institute and State University.

Completed
Registry status
NA
Development phase
40
Enrollment target

NCT03273673: Completed NA study, sponsored by Virginia Polytechnic Institute and State University.

NCT03273673 is a NA study that has completed, run by Virginia Polytechnic Institute and State University. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03273673, a NA study, has completed, sponsored by Virginia Polytechnic Institute and State University.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

ACL injuries are common among athletes and due to residual muscle weakness, limited knee motion and asymmetrical movement patterns after surgery many of these athletes will sustain secondary ACL injuries following return to sports. This project seeks to determine if a novel biofeedback-based rehabilitation approach can decrease a known risk factor for secondary injuries to the ACL. The project specifically focuses on correcting asymmetric movement patterns, a known risk factor for secondary injury that is not directly addressed by existing interventions through a 6 week therapy based biofeedback intervention.

Primary Outcome

The peak knee extension moment asymmetry will be assessed during the first landing of a stop-jump task

Interventions

  • OTHER Biofeedback Intervention

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2018-03-20
Est. Completion 2020-05-05
Phase NA

What the finished NCT03273673 record still lists

NCT03273673 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Biofeedback Intervention is the first listed.

NCT03273673 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03273673 about?

NCT03273673 is a clinical study titled "Reduction of Risk Factors for ACL Re-injuries Using a Novel Biofeedback Approach". ACL injuries are common among athletes and due to residual muscle weakness, limited knee motion and asymmetrical movement patterns after surgery many of these athletes will sustain secondary ACL injuries following return to sports. This project seeks to determine if a novel biofeedback-based rehabil...

What is the current status of trial NCT03273673?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2018-03-20. Estimated completion is 2020-05-05.

What interventions are being tested in trial NCT03273673?

The interventions under investigation include: Biofeedback Intervention (OTHER).

Who is sponsoring clinical trial NCT03273673?

This trial is sponsored by Virginia Polytechnic Institute and State University, which has 104 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03273673's enrollment target sits among peer trials

40 1447th of 2000 higher than 465 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01306019 · 40 participants · Phase 1

    Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)

  • NCT01608152 · 40 participants

    Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors

  • NCT01668082 · 40 participants · NA

    An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection

  • NCT02015013 · 40 participants · Phase 2

    Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03273673, the US trial registry maintained by the National Library of Medicine. NCT03273673 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.