RECRUITING

Micro-Doppler Radar: A Gold Standard Comparison

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to see if the study team can use micro-Doppler signal (MDS) technology to determine if someone has had an anterior cruciate ligament (ACL) reconstruction. The investigators will do this by comparing the movement data from a group of people who have had the surgery with a group who has not had the surgery to see if the micro-Doppler radar technology can accurately and predictably tell the difference.

Official Title

The Use of Micro-Doppler Radar to Identify Service Members at Risk for Musculoskeletal Injury: A Gold Standard Comparison

Quick Facts

Study Start:2023-02-21
Study Completion:2025-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05521126

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * age 18-40
  2. * history of ACL reconstruction
  3. * no current musculoskeletal injuries
  4. * ACL repair between 9 and 24 months prior to recruitment
  5. * age 18-40
  6. * never had lower extremity surgery
  1. * age \<18 or \>40
  2. * pregnancy
  3. * institutionalization
  4. * history of cerebral vascular accident
  5. * unable to provide informed consent
  6. * inability to perform study activities
  7. * history of hip or knee replacement
  8. * inability to walk or jump without a limp
  9. * current neuromuscular disease
  10. * any surgery in the last 6 months
  11. * age \< 18 or \> 40
  12. * pregnancy
  13. * institutionalization
  14. * history of Cerebral Vascular Accident
  15. * unable to provide informed consent
  16. * inability to perform study activities
  17. * history of knee or hip replacement
  18. * inability to walk or jump without a limp
  19. * current neuromuscular disease
  20. * history of lower extremity surgery
  21. * any surgery in the last 6 months

Contacts and Locations

Study Contact

Leonard A Kishel, MA
CONTACT
717-531-0003
lkishel@pennstatehealth.psu.edu

Principal Investigator

Cayce A Onks, DO, MS
PRINCIPAL_INVESTIGATOR
Milton S. Hershey Medical Center

Study Locations (Sites)

Lebanon Valley College
Annville, Pennsylvania, 17003
United States
Pennsylvania State University College of Medicine
Hershey, Pennsylvania, 17033
United States

Collaborators and Investigators

Sponsor: Milton S. Hershey Medical Center

  • Cayce A Onks, DO, MS, PRINCIPAL_INVESTIGATOR, Milton S. Hershey Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-02-21
Study Completion Date2025-02

Study Record Updates

Study Start Date2023-02-21
Study Completion Date2025-02

Terms related to this study

Keywords Provided by Researchers

  • musculoskeletal injury
  • anterior cruciate ligament injury
  • anterior cruciate ligament repair
  • micro-Doppler radar
  • motion capture

Additional Relevant MeSH Terms

  • Musculoskeletal Injury
  • Anterior Cruciate Ligament Injuries