RECRUITING

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

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

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.

Official Title

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

Quick Facts

Study Start:2022-10-17
Study Completion:2025-01-17
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05652946

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 CriteriaExclusion Criteria
  1. 1. Currently admitted for inpatient rehabilitation at Rehabilitation Hospital Overland Park with neurological diagnosis.
  2. 2. At least 18 years of age.
  3. 3. Predicted length of stay to be at least 7 days.
  4. 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. 5. Able to fit into at least one device.
  6. 6. Screened and cleared by a physician.
  7. 7. Cognitively intact to communicate pain and/or need to stop session, and able to follow simple commands.
  1. 1. Current or history of other medical conditions that could affect the outcome measures.
  2. 2. Currently involved in another intervention study.
  3. 3. Any absolute contraindication listed for each device used.
  4. 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.

Contacts and Locations

Study Contact

Jeana R Young, AAS
CONTACT
913-967-5289
jyoung2@pamrehab.com
Leslie R VanHiel, DScPT
CONTACT
404-226-8017
leslie.vanhiel@gmail.com

Principal Investigator

Brett Schoen, MD
PRINCIPAL_INVESTIGATOR
Rehabilitation Hospital of Overland Park

Study Locations (Sites)

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

Collaborators and Investigators

Sponsor: Rehabilitation Hospital of Overland Park

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

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 Date2022-10-17
Study Completion Date2025-01-17

Study Record Updates

Study Start Date2022-10-17
Study Completion Date2025-01-17

Terms related to this study

Keywords Provided by Researchers

  • Advanced Rehabilitation Technology
  • Therapeutic Device
  • Robotic Rehabilitation Research
  • Health Economics
  • Functional Outcomes

Additional Relevant MeSH Terms

  • Neurologic Disorder