Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05488054
Other study ID # 20191389
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 8, 2022
Est. completion date June 2025

Study information

Verified date November 2023
Source University Hospitals Cleveland Medical Center
Contact James Voos, MD
Phone 216-844-0209
Email james.voos@UHhospitals.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will utilize the Moxy wearable sensor to measure muscle oxygen saturation levels in athletes following lower extremity surgery (ACL or Hip arthroscopy) to evaluate their Return-to-Play. The acquired data will complement current protocols utilized by Dr. Voos and Dr. Salata in this regard and will add quantifiable evidence to enable a robust measurement of the surgical limb versus non-surgical limb.


Description:

Patients with a diagnosis of ACL tear or hip pathology will undergo surgery. Following surgery, patients will report to clinic for scheduled physical therapy per their institution's injury-specific physical therapy protocol. At set time points (6-week, 12-week, 6 months, and 9 months) during their recovery, patients will be assessed for muscle oxygen saturation and hemoglobin levels with the Moxy sensor. This sensor is a non-invasive device placed over the rectus femoris to monitor oxygen and hemoglobin levels. The patient will then follow the therapy as instructed by the physical therapist and perform the protocol-specific exercises with the sensor in place. The measured parameters will be recorded and stored per patient. The injured patients will be compared to healthy control patients undergoing a similar one-hour exercise session while wearing the Moxy sensor for comparison of results. The goal of this study is to use the data obtained from the Moxy sensor device to further predict recovery of function in muscles supporting injured soft tissues to determine safe return to sport.


Recruitment information / eligibility

Status Recruiting
Enrollment 226
Est. completion date June 2025
Est. primary completion date June 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 14 Years to 30 Years
Eligibility Inclusion Criteria: - Age range: Patients age 14 to 30 years - Patients with ACL injury requiring surgical correction - Patients undergoing arthroscopic hip surgery - Healthy individuals with no history of ACL, arthroscopic knee or arthroscopic hip surgery Exclusion Criteria: - Patients below 14 years or above 30 years - Non-English-speaking subjects - Pregnant individuals

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Physical Therapy
Patients will undergo physical therapy following surgical intervention
Monitored Work-out
Healthy volunteers will undergo a monitored workout for comparison of data
Device:
Moxy Oxygen Sensor Device
Individuals will wear a Moxy sensor device during workouts to monitor oxygen and hemoglobin levels in their muscles

Locations

Country Name City State
United States University Hospitals Physical Therapy Avon Ohio
United States University Hospitals Cleveland Medial Center Cleveland Ohio

Sponsors (1)

Lead Sponsor Collaborator
University Hospitals Cleveland Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in O2 Saturation levels as measured by Moxy Sensor device 6 months, 9 months, 12 months (once for healthy individuals)
Primary Changes in hemoglobin levels as measured by Moxy Sensor device 6 months, 9 months, 12 months (once for healthy individuals)
See also
  Status Clinical Trial Phase
Recruiting NCT04519801 - BFR Therapy for Post-Op Rehab of ACL Reconstruction With Quadriceps Tendon Autograft N/A
Withdrawn NCT03389685 - Can PRP Reduce Pro-Inflammatory Biomarkers Following ACL Injury Phase 2
Recruiting NCT04958733 - Does Bone Grafting at the Time of Bone-Patellar Tendon-Bone ACL Reconstruction Reduce the Incidence of Post-operative Anterior Knee Pain: A Randomized Controlled Clinical Study N/A
Terminated NCT04101682 - Continuous Vs Single Shot Block After ACL Early Phase 1
Not yet recruiting NCT05374382 - A Prehab Strengthening Program Prior to ACL Surgery on Lower Limb Structure and Function N/A
Not yet recruiting NCT04068701 - Real-time Sensorimotor Feedback for Injury Prevention in Males Assessed in Virtual Reality N/A
Recruiting NCT03479775 - Muscle Function and Traumatic Knee Injury in Sports
Not yet recruiting NCT05498285 - Post-ACL Reconstruction Rehab UPSCALER App RCT HPUPM N/A
Recruiting NCT05461625 - ACL Reconstruction With/Without ALL Reconstruction N/A
Active, not recruiting NCT03491046 - Molecular Imaging Assessment of ACL Viability N/A
Withdrawn NCT04342000 - The Effect of Movement Education on Jumping/Landing Quality in High School Athletes N/A
Completed NCT04993339 - Clinical Outcomes of ACL Reconstruction Augmented by an Injectable Osteoconductive/Osteoinductive Compound Phase 3
Withdrawn NCT03614351 - Dietary Protein Intake and Rehabilitation From Anterior Cruciate Ligament Surgery N/A
Withdrawn NCT03670550 - Dynamic ACL Brace: In Vivo Kinematics N/A
Recruiting NCT06430775 - Exploring Prolonged AMR in ACL Reconstructed Patients
Recruiting NCT06206200 - The Effect of Cognitive Dual-task Rehabilitation on Arthrogenic Muscle Responses After ACL Reconstruction N/A
Active, not recruiting NCT06167343 - Comparison of Semitendinosus and Quadriceps Grafts for Anterior Cruciate Ligament Reconstruction N/A
Completed NCT04541940 - TeleRehabilitation Following ACL Reconstruction N/A
Terminated NCT03497780 - Longitudinal Assessment of Cartilage Injury and Remodeling After Anterior Cruciate Ligament Rupture and Reconstruction:
Completed NCT04967937 - Neuromuscular Training Improves Single-Limb Stability N/A