Remote Rehabilitation Via the Internet in Patients After a Stroke - Physical Rehabilitation Using Biofeedback Systems to Improve Upper Extremity Function

NCT ID: NCT01696864

Last Updated: 2017-01-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-31

Study Completion Date

2016-12-31

Brief Summary

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The objective of this study is to examine monitored rehabilitation therapy over the internet to improve upper limb function for stroke patients. Home rehabilitation for stroke patients will avoid the burden of arrival to the health facilities, making it easier on them and improve their quality of life and the lives of their caregivers. To achieve this goal the investigators will examine the effectiveness and feasibility of home rehabilitation system of upper limb, consisting of ergonomic accessories (hand and arm tutors).

The quantitative indices will be based on the quantitative clinical measures that are used in regular evaluations of stroke patients and function and range of motion indices as received from the system.

Detailed Description

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Conditions

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Stroke Patients

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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stroke patients - hand

stroke patients with the ability to move their hand

Group Type EXPERIMENTAL

Hand tutor rehabilitation device

Intervention Type DEVICE

A rehabilitation device for the hand

stroke patient - arm

stroke patients with the ability to move their arms

Group Type EXPERIMENTAL

Arm tutor rehabilitation device

Intervention Type DEVICE

A rehabilitation device for the arm

Interventions

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Hand tutor rehabilitation device

A rehabilitation device for the hand

Intervention Type DEVICE

Arm tutor rehabilitation device

A rehabilitation device for the arm

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Stroke patients who had at least eight conventional rehabilitation treatments lasted at least until a month before the start of the experiment,
* not affected cognitively (to be determined by the score on the mini mental exam greater than 23).
* patients have daily access to a computer and the Internet, and use a personal caregiver or family member can supervise the use of the system.

Exclusion Criteria

* Global or sensory aphasia, unilateral spatial neglect, apraxia and other acute neurological or orthopedic conditions.
Minimum Eligible Age

30 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sheba Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Gabi Zeilig, Dr.

Role: PRINCIPAL_INVESTIGATOR

Sheba Medical Center

Locations

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Sheba Medical Center rehabilitation facility

Ramat Gan, , Israel

Site Status

Countries

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Israel

Other Identifiers

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SHEBA-12-9471-GZ-CTIL

Identifier Type: -

Identifier Source: org_study_id

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