COMPLETED

Rehabilitation Strategies to Improve Outcomes For Patients With a Lower Extremity Fracture

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 evaluate speed high intensity interval training (HIIT) walking program following an orthopedic trauma.

Official Title

Rehabilitation Strategies to Improve Outcomes For Patients With a Lower Extremity Fracture

Quick Facts

Study Start:2022-03-03
Study Completion:2025-12-18
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05274022

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 50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Ability to read and speak English
  2. * Acute orthopedic injury to the femoral or tibial shaft requiring surgical fixation with an intramedullary rod
  3. * Age 18-50 years of age
  1. * History of chronic pain defined as pain lasting more than 3 months and bothersome at least half the days over the past 6 months that started before the fracture
  2. * Moderate or severe traumatic brain injury
  3. * Initial treatment requiring amputation
  4. * Not employed at the time of the accident at least 20 hours per week.
  5. * Spinal cord injury
  6. * History of schizophrenia, dementia or neurologic disorder with peripheral dysfunction
  7. * Non ambulatory or limited ability to walk without an assistive device prior to the fracture
  8. * Multiple trauma that prevents early weight bearing
  9. * Current Pregnancy
  10. * Unable to participate in or complete in-person follow-up visits or therapy sessions
  11. * In outpatient Physical Therapy at the start of the intervention
  12. * Use of an assistive device to walk for community ambulation at the 10-12 weeks post hospital discharge time point

Contacts and Locations

Principal Investigator

Brian Noehren, Ph.D.
PRINCIPAL_INVESTIGATOR
University of Kentucky

Study Locations (Sites)

University of Kentucky
Lexington, Kentucky, 40506
United States
Vanderbilt University
Nashville, Tennessee, 37203
United States

Collaborators and Investigators

Sponsor: Brian W. Noehren

  • Brian Noehren, Ph.D., PRINCIPAL_INVESTIGATOR, University of Kentucky

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 Date2022-03-03
Study Completion Date2025-12-18

Study Record Updates

Study Start Date2022-03-03
Study Completion Date2025-12-18

Terms related to this study

Keywords Provided by Researchers

  • Surgical fixation
  • High intensity interval training

Additional Relevant MeSH Terms

  • Femoral Fracture
  • Tibial Fractures