Telerehabilitation for the Hand and Arm After Stroke and Traumatic Brain Injury

Sponsor
Ono Academic College (Other)
Overall Status
Unknown status
CT.gov ID
NCT00295399
Collaborator
(none)
2

Study Details

Study Description

Brief Summary

The goal of this project is to develop a low-cost, user-friendly, portable telerehabilitation system for physical therapy of the upper limb after stroke or traumatic brain injury. The system is based on the use of a commercially available force feedback joystick and will work with an ordinary home PC and a standard high-speed internet connection. Using the joystick, the patient will perform exercises designed to aid in recovering motor function of the hand and arm. The joystick will be programmed to either assist or resist the patient's movements. The system will include sophisticated analysis of patient status and progress to provide the therapist and physician with detailed information. In the first phase of the study, we will develop the system in cooperation with the physical therapy staff and other rehabilitation specialists. The investigators will examine the usability, comfort, safety and therapeutic benefit of the system. In the second phase of the study, the investigators will employ the system in patients' homes, using the internet to connect to rehabilitation specialists in the clinic. The study hypothesis is that it is possible to adapt commercially available, low cost gaming equipment such as force feedback joysticks to provide therapy for patients in their own homes, and that patients will be able to work with this system and will find it enjoyable and helpful for recovering motor function.

Condition or Disease Intervention/Treatment Phase
  • Device: The Jerusalem Telerehabilitation System
N/A

Study Design

Study Type:
Interventional
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment

Outcome Measures

Primary Outcome Measures

  1. Modified motor assessment scale []

  2. Kinematic analysis []

  3. Feedback questionnaires for patients, therapists and caretakers []

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Post-cerebrovascular accident or post-traumatic brain injury

  • In medically stable condition

  • Resident in Israel

Note: In addition there will be healthy, age-matched volunteers

Exclusion Criteria:
  • History of psychiatric illness

  • Grade of less than 23 in the Mini-Mental Test

  • Inability to understand informed consent form

  • Inability to follow 3-step instructions

  • Pregnancy

  • Receptive aphasia

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hadassah Medical Organization Jerusalem Israel 91120
2 Chaim Sheba Medical Center Tel Hashomer Israel 52662

Sponsors and Collaborators

  • Ono Academic College

Investigators

  • Study Chair: Heidi Sugarman, Ph.D., Ono Academic College
  • Principal Investigator: Joseph Tiran, PhD, Ben Gurion University, Beer Sheva, Israel
  • Principal Investigator: Ehud Dayan, BSc, Sonarion Hadassah Virtual Reality Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00295399
Other Study ID Numbers:
  • JTRS001
First Posted:
Feb 23, 2006
Last Update Posted:
Aug 13, 2008
Last Verified:
Aug 1, 2008

Study Results

No Results Posted as of Aug 13, 2008