NCT00295399

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.

Trial Health

55
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

2 active sites

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 21, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

February 23, 2006

Completed
Last Updated

August 13, 2008

Status Verified

August 1, 2008

First QC Date

February 21, 2006

Last Update Submit

August 11, 2008

Conditions

Keywords

cerebrovascular accidenttraumatic brain injurystroketelerehabilitation

Outcome Measures

Primary Outcomes (3)

  • Modified motor assessment scale

  • Kinematic analysis

  • Feedback questionnaires for patients, therapists and caretakers

Interventions

Eligibility Criteria

Age20 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Hadassah Medical Organization

Jerusalem, 91120, Israel

Location

Chaim Sheba Medical Center

Tel Litwinsky, 52662, Israel

Location

Related Publications (1)

  • Sugarman H, Dayan E, Weisel-Eichler A, Tiran J. The Jerusalem TeleRehabilitation System, a new low-cost, haptic rehabilitation approach. Cyberpsychol Behav. 2006 Apr;9(2):178-82. doi: 10.1089/cpb.2006.9.178.

    PMID: 16640475BACKGROUND

MeSH Terms

Conditions

StrokeBrain Injuries, Traumatic

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesBrain InjuriesCraniocerebral TraumaTrauma, Nervous SystemWounds and Injuries

Study Officials

  • Heidi Sugarman, Ph.D.

    Ono Academic College

    STUDY CHAIR
  • Joseph Tiran, PhD

    Ben Gurion University, Beer Sheva, Israel

    PRINCIPAL INVESTIGATOR
  • Ehud Dayan, BSc

    Sonarion Hadassah Virtual Reality Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Heidi Sugarman, Ph.D.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

February 21, 2006

First Posted

February 23, 2006

Last Updated

August 13, 2008

Record last verified: 2008-08

Locations