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

NCT05007366 · ClinicalTrials.gov registry record · NA

Optimizing Gait Biomechanics for Posttraumatic Osteoarthritis Prevention

A NA study, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
NA
Development phase
24
Enrollment target

NCT05007366: Completed NA study, sponsored by University of North Carolina, Chapel Hill.

NCT05007366 is a NA study that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 24 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05007366, a NA study, has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
NA
Development phase
24 participants
Enrollment target

Study Summary

The purpose of this study is to report the feasibility and determine the initial effects of 18 sessions of real-time gait biofeedback delivered over a 6-week period on retention and transfer of normalized gait biomechanics and improvements in indicators of early post-traumatic osteoarthritis development in those with an anterior cruciate ligament reconstruction (ACLR) at 6 and 8-week posttests.

Primary Outcome

The investigators will record the number of participants who were recruited, the frequency at which they were recruited, and where they were recruited from. Range 0-70. Higher number indicates more completion.

Interventions

  • BEHAVIORAL Real-time gait biofeedback
  • BEHAVIORAL Sham real-time gait biofeedback

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2021-08-05
Est. Completion 2022-12-02
Phase NA

What the finished NCT05007366 record still lists

NCT05007366 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Real-time gait biofeedback is the first listed.

NCT05007366 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05007366 about?

NCT05007366 is a clinical study titled "Optimizing Gait Biomechanics for Posttraumatic Osteoarthritis Prevention". The purpose of this study is to report the feasibility and determine the initial effects of 18 sessions of real-time gait biofeedback delivered over a 6-week period on retention and transfer of normalized gait biomechanics and improvements in indicators of early post-traumatic osteoarthritis develop...

What is the current status of trial NCT05007366?

This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2021-08-05. Estimated completion is 2022-12-02.

What interventions are being tested in trial NCT05007366?

The interventions under investigation include: Real-time gait biofeedback (BEHAVIORAL), Sham real-time gait biofeedback (BEHAVIORAL).

Who is sponsoring clinical trial NCT05007366?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05007366's enrollment target sits among peer trials

24 1736th of 2000 higher than 246 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

  • NCT02331979 · 24 participants · NA

    Improving Bladder Function in SCI by Neuromodulation

  • NCT03096197 · 24 participants · NA

    Exoskeleton and Spinal Cord Stimulation for SCI

  • NCT03223922 · 24 participants · NA

    Neurocognitive Functioning With Genu-Sparing Whole Brain Radiation Therapy for Brain Metastases

  • NCT03326921 · 24 participants · Phase 1

    HA-1 T TCR T Cell Immunotherapy for the Treatment of Patients With Relapsed or Refractory Acute Leukemia After Donor Stem Cell Transplant

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 NCT05007366, the US trial registry maintained by the National Library of Medicine. NCT05007366 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.