IISART (International Industry Society of Advanced Rehabilitation Technology) Advanced Rehabilitation Technology Study

Description

A pre-post, randomized control trial comparing cost-effective and functional outcomes of participants with neurological diagnoses using robotic devices and advanced technology during inpatient rehabilitation to the outcomes of control participants without the use of robotic devices and advanced technology during rehabilitation. We aim to show at least similar inpatient rehabilitation outcomes and improved health economics in participants with neurological diagnoses by using robotic devices and advanced technology to increase the intensity and dose of rehabilitation.

Conditions

Neurologic Disorder

Talk to us

Study Overview

On this page

Study Details

Study overview

A pre-post, randomized control trial comparing cost-effective and functional outcomes of participants with neurological diagnoses using robotic devices and advanced technology during inpatient rehabilitation to the outcomes of control participants without the use of robotic devices and advanced technology during rehabilitation. We aim to show at least similar inpatient rehabilitation outcomes and improved health economics in participants with neurological diagnoses by using robotic devices and advanced technology to increase the intensity and dose of rehabilitation.

Clinicians, Academics, Industry, and Insurance Collaborate to Assess Cost-Effectiveness and Functional Outcomes Using Advanced Rehabilitation Technology

IISART (International Industry Society of Advanced Rehabilitation Technology) Advanced Rehabilitation Technology Study

Condition
Neurologic Disorder
Intervention / Treatment

-

Contacts and Locations

Overland Park

Rehabilitation Hospital of Overland Park, Overland Park, Kansas, United States, 66207

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Currently admitted for inpatient rehabilitation at Rehabilitation Hospital Overland Park with neurological diagnosis.
  • 2. At least 18 years of age.
  • 3. Predicted length of stay to be at least 7 days.
  • 4. Able to tolerate upright sitting without orthostatic hypotension for upper extremity, cycling, and sitting balance devices AND/OR able to tolerate upright standing for at least 15 minutes without orthostatic hypotension for walking and standing balance devices.
  • 5. Able to fit into at least one device.
  • 6. Screened and cleared by a physician.
  • 7. Cognitively intact to communicate pain and/or need to stop session, and able to follow simple commands.
  • 1. Current or history of other medical conditions that could affect the outcome measures.
  • 2. Currently involved in another intervention study.
  • 3. Any absolute contraindication listed for each device used.
  • 4. Any pre-existing physical or medical condition that the Physiatrist determines would significantly limit a patient's ability to benefit from or continue in the study.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Rehabilitation Hospital of Overland Park,

Brett Schoen, MD, PRINCIPAL_INVESTIGATOR, Rehabilitation Hospital of Overland Park

Study Record Dates

2025-01-17