Actively Recruiting

Phase Not Applicable
Age: 14Years - 30Years
All Genders
Healthy Volunteers
ID05488054

Use of a Wearable Muscle Oxygen Saturation Sensor in the Rehabilitation of High-School and Collegiate Athletes Recovering From Arthroscopic Hip and Knee Surgery

Led by University Hospitals Cleveland Medical Center · Updated on 2025-12-24

226

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate muscle oxygen saturation and hemoglobin levels in athletes recovering from arthroscopic surgery of the knee or hip, such as ACL tears or hip pathology. The study focuses on measuring recovery progress to support decisions on safe return-to-play. Data from patients undergoing surgery and healthy individuals are compared to enhance understanding of muscle function during rehabilitation. Participants will wear a Moxy sensor device, a non-invasive wearable that monitors oxygen and hemoglobin levels in the rectus femoris muscle during workouts and therapy sessions. Surgical patients will follow their institution's injury-specific physical therapy protocols, with assessments at set intervals: 6 weeks, 12 weeks, 6 months, and 9 months post-surgery. Healthy volunteers will perform a monitored one-hour exercise session for baseline comparison. Throughout the study, muscle oxygen saturation and hemoglobin levels will be recorded at the specified time points. Researchers will use this data to predict muscle function recovery in injured limbs compared to non-injured limbs and healthy controls. The trial will last up to 9 months for surgical patients, with a single assessment for healthy volunteers. Safety and progress will be monitored during regular clinic visits and physical therapy sessions.

CONDITIONS

Brief Title

Muscle O2 Saturation and Hemoglobin Levels During Rehabilitation From Arthroscopic Surgery

Who Can Participate

Age: 14Years - 30Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • Patients below 14 years or above 30 years
  • Non-English-speaking subjects
  • Pregnant individuals

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.

Surgery

Duration - Day of surgery

Participants who require arthroscopic ACL or hip surgery will undergo the surgical procedure.

1 visit (in-person)

Treatment

Duration - Up to 9 months

Participants will undergo physical therapy following surgery and wear a Moxy sensor device during therapy sessions to monitor muscle oxygen saturation and hemoglobin levels.

Physical therapy sessions per institution’s protocol with sensor monitoring at 6-week, 12-week, 6-month, and 9-month visits

Monitored Workout for Healthy Controls

Duration - Single session

Healthy individuals will undergo a monitored one-hour workout wearing the Moxy sensor device to provide baseline comparison data.

1 workout visit (in-person)

Follow-up Assessments

Duration - Up to 12 months

Participants will have follow-up assessments to measure muscle oxygen saturation and hemoglobin levels with the Moxy sensor at 6 months, 9 months, and 12 months (healthy controls only) to evaluate recovery and compare to baseline.

Visits at 6 months, 9 months, and 12 months for healthy controls

Trial Site Locations

Total: 2 locations

1

University Hospitals Physical Therapy

Avon, Ohio, United States, 44011

Not Yet Recruiting

2

University Hospitals Cleveland Medial Center

Cleveland, Ohio, United States, 44106

Actively Recruiting

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Research Team

J

James Voos, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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