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Force Feedback Joystick in Upper Limb Rehabilitation Following Stroke

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Clalit Health Services

Status

Unknown

Conditions

Stroke

Treatments

Device: Exercise with force feedback joystick

Study type

Interventional

Funder types

Other

Identifiers

NCT00758147
BGC085012CTIL

Details and patient eligibility

About

The purpose of this study is to assess the influence of force feedback joysticks and haptic feedback in improving upper limb rehabilitation outcomes following stroke.

Full description

Upper limb paresis or plegia following stroke remains a significant cause of impairment and disability. Regaining function requires learning through repetitive movements and activities of daily living(ADLs).

The aim of the study in this application is to test the usability of the system in specialized rehabilitation hospital settings. In this first stage of development, after developing and testing the system together with expert physiotherapists, we will examine the system for usability (is it "user friendly"), comfort level, and therapeutic efficacy.

The system consists of an ordinary PC computer, specially written software, and a commercially available force feedback joystick. (Force feedback joysticks, are usually used for gaming; they contain miniature motors that allow the joystick to either help or resist the movements of the person using it). Patients who are unable to grasp the joystick will use a specially built arm rest that is attached to an ordinary office chair without wheels. Patients rest their forearm on the arm rest and thus can manipulate the joystick by means of movement of the shoulder and elbow joints instead of by movements of the wrist, since wrist movements are often difficult for brain damaged individuals.

Enrollment

30 estimated patients

Sex

All

Ages

65 to 86 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Medically stable post first stroke patients
  • Score of more than 17 on the Mini Mental Scale Test(MMST)

Exclusion criteria

  • A history of psychiatric illness
  • Inability to understand the informed consent form
  • Inability to understand and follow 2-3 step instructions
  • Receptive aphasia (sensory aphasia)

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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