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Rapid Rehabilitation to Treat Lower Extremity Trauma

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Mayo Clinic

Status

Enrolling

Conditions

Lower Limb Trauma

Treatments

Behavioral: Promis Physical Function Questionnaire
Behavioral: L Test
Behavioral: Narrowing Beam Walking Test
Behavioral: PEQ-A

Study type

Interventional

Funder types

Other

Identifiers

NCT05225792
21-010009

Details and patient eligibility

About

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.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion 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.

Exclusion criteria

  • Subjects must not have excessive pain or other neuromuscular problems that preclude them from performing the test protocol.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

Injured Service Members
Experimental group
Treatment:
Behavioral: PEQ-A
Behavioral: Narrowing Beam Walking Test
Behavioral: L Test
Behavioral: Promis Physical Function Questionnaire

Trial contacts and locations

1

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Central trial contact

Christine Huyber, CCRP

Data sourced from clinicaltrials.gov

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