RECRUITING

Rapid Rehabilitation to Treat Lower Extremity Trauma

Conditions

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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 find out if an advance balance perturbation training program can enhance the rehabilitation process by increasing weight-bearing strategies on the prosthetic or injured limb, and, help reduce stumbles and falls.

Official Title

Improved Training Method for Advanced Rehabilitation of Warfighters With Lower Extremity Trauma

Quick Facts

Study Start:2024-01-08

Study Completion:2026-04

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05225792

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

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Research participants will be eligible active duty service members and retired veterans. * Having lower limb trauma (transtibial and transfemoral amputations, bilateral amputations, and limb salvage). * Are enrolled in conventional rehabilitation at the participating military treatment centers. * Subjects with dysvascular disease will be excluded because compromised lower limb somatosensation and circulation are independently linked with poor postural stability and a history of frequent falls. * For subjects with amputations, the individual must be a community ambulator (i.e., K-Level 3 or 4). * For subjects with limb salvage, they will need to have an IDEO and be entered into the Return-to-Run training program.	Pregnancy or breastfeeding Severe psychiatric disorders Active substance abuse Unstable medical conditions Inability to comply with study requirements

Inclusion Criteria

Exclusion Criteria

* Research participants will be eligible active duty service members and retired veterans.
* Having lower limb trauma (transtibial and transfemoral amputations, bilateral amputations, and limb salvage).
* Are enrolled in conventional rehabilitation at the participating military treatment centers.
* Subjects with dysvascular disease will be excluded because compromised lower limb somatosensation and circulation are independently linked with poor postural stability and a history of frequent falls.
* For subjects with amputations, the individual must be a community ambulator (i.e., K-Level 3 or 4).
* For subjects with limb salvage, they will need to have an IDEO and be entered into the Return-to-Run training program.

Pregnancy or breastfeeding
Severe psychiatric disorders
Active substance abuse
Unstable medical conditions
Inability to comply with study requirements

Contacts and Locations

Study Contact

Christine Huyber, CCRP

CONTACT

(507) 266-0984

Huyber.Christine@mayo.edu

Principal Investigator

Kenton Kaufman, PhD

PRINCIPAL_INVESTIGATOR

Mayo Clinic

Study Locations (Sites)

Mayo Clinic in Rochester

Rochester, Minnesota, 55905

United States

Collaborators and Investigators

Sponsor: Mayo Clinic

Kenton Kaufman, PhD, PRINCIPAL_INVESTIGATOR, Mayo Clinic

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 Date2024-01-08

Study Completion Date2026-04

Study Record Updates

Study Start Date2024-01-08

Study Completion Date2026-04

Terms related to this study

Additional Relevant MeSH Terms

Lower Limb Trauma