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NCT05968729 · ClinicalTrials.gov registry record · NA

Assessment of Gait Adaptation Due to an Asymmetric Walking Protocol

A NA study of Anterior Cruciate Ligament Reconstruction, sponsored by University of Connecticut.

Recruiting
Registry status
NA
Development phase
40
Enrollment target
1
Study location

NCT05968729 is a NA study of Anterior Cruciate Ligament Reconstruction that is actively recruiting participants, run by University of Connecticut. The registered enrollment target is 40 participants, below the 291-participant average among 11 other Anterior Cruciate Ligament Reconstruction trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05968729, a NA study of Anterior Cruciate Ligament Reconstruction, is actively recruiting participants, sponsored by University of Connecticut.

RECRUITING
Registry status
NA
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

The purpose of this work is to conduct a comparative research-focused study to evaluate the effectiveness of how purposefully induced asymmetric walking protocols restore healthy, symmetric limb loading in individuals following post-anterior cruciate ligament reconstruction (ACLR) surgery. Additionally, computational modeling and machine learning to model knee loading in the clinic to determine the optimal asymmetric walking protocol to restore healthy gait in post-ACLR individuals.

Interventions

  • OTHER Active Comparator: 0.25 m/s asymmetric session first
  • OTHER Active Comparator: 0.50 m/s asymmetric session first

Study Locations (1)

Connecticut

  • University of Connecticut - Storrs

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2022-09-01
Est. Completion 2027-07-31
Phase NA

Sponsor

University of Connecticut

107 total trials

What the Registry Record Tells You About NCT05968729

The ClinicalTrials.gov registry entry for NCT05968729 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 291-participant average among 11 other Anterior Cruciate Ligament Reconstruction trials with a reported enrollment target (86% lower). The listed sponsor is University of Connecticut, which has 107 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Anterior Cruciate Ligament Reconstruction appearing as the primary indexed condition, and to 2 interventions - of which Active Comparator: 0.25 m/s asymmetric session first is the first listed.

NCT05968729 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.

Frequently Asked Questions

What is clinical trial NCT05968729 about?

NCT05968729 is a clinical study titled "Assessment of Gait Adaptation Due to an Asymmetric Walking Protocol". The purpose of this work is to conduct a comparative research-focused study to evaluate the effectiveness of how purposefully induced asymmetric walking protocols restore healthy, symmetric limb loading in individuals following post-anterior cruciate ligament reconstruction (ACLR) surgery. Additiona...

What is the current status of trial NCT05968729?

This trial is currently recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2022-09-01. Estimated completion is 2027-07-31.

What conditions does trial NCT05968729 study?

This clinical trial studies the following conditions: Anterior Cruciate Ligament Reconstruction.

What interventions are being tested in trial NCT05968729?

The interventions under investigation include: Active Comparator: 0.25 m/s asymmetric session first (OTHER), Active Comparator: 0.50 m/s asymmetric session first (OTHER).

Who is sponsoring clinical trial NCT05968729?

This trial is sponsored by University of Connecticut, which has 107 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05968729 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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