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

Sponsor
Sheba Medical Center (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01696864
Collaborator
(none)
0
1
2
9
0

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Hand tutor rehabilitation device
  • Device: Arm tutor rehabilitation device
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Remote Rehabilitation Via the Internet in Patients After a Stroke - Physical Rehabilitation Using Biofeedback Systems to Improve Upper Extremity Function
Study Start Date :
Mar 1, 2016
Actual Primary Completion Date :
Dec 1, 2016
Actual Study Completion Date :
Dec 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: stroke patients - hand

stroke patients with the ability to move their hand

Device: Hand tutor rehabilitation device
A rehabilitation device for the hand

Experimental: stroke patient - arm

stroke patients with the ability to move their arms

Device: Arm tutor rehabilitation device
A rehabilitation device for the arm

Outcome Measures

Primary Outcome Measures

  1. Fugl-Meyer Assessment upper extremity part (FMA) [10 minutes]

    The FMA assesses the motor impairment of the upper extremity after stroke. Each movement is graded on a 3-point scale, and the total score for the upper extremity ranges from 0-60 points where a higher score represents more active movements. An additional part assesses the coordination of the affected upper extremity and the score ranges between 0-6 where a higher score represents poorer coordination ability. This test is one of the most commonly used instruments in rehabilitation and its validity and reliability have been well established

  2. Arm and Hand Activity Inventory (CAHAI) [10 minutes]

    The test assesses the functional ability of the affected arm and hand of people with stroke. The abbreviated version includes 7 functional activities (e.g. open a jar of coffee) that require bilateral use of the upper extremities as well various types of grip. The score range between1 and 7

  3. Motor Activity Log (MAL) [10 minutes]

    The MAL consist of a semi structured interview for the patient to assess the use of the paretic arm and hand during daily activities. Two scores on a scale of 1 -5, are given for each activity;for the amount of use (AOU) and for the quality of movement (QOM). Usability of the system i.e. ease of use of the system

  4. System Usability Scale (SUS) [10 minutes]

    This questionnaire includes 10 items rated on a 5 points scale, which provide a global view of subjective assessment of a system's usability. The item scores were calculated to give an overall score ranging from 10 to 100 points. The SUS has been shown to be a robust and reliable evaluation tool

  5. Box& Block Test of Manual Dexterity [10 minutes]

    This is a valid and reliable test which is used to assess hand dexterity. In addition it is used to assess endurance of the upper extremity. The subject is asked to transfer cubes, above a partition, from one side of a box to the other for one minute with both hands. The score is the number of cubes that were transferred. In addition: Range of motion of fingers, wrist elbow and shoulder as measured by the devices

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sheba Medical Center rehabilitation facility Ramat Gan Israel

Sponsors and Collaborators

  • Sheba Medical Center

Investigators

  • Principal Investigator: Gabi Zeilig, Dr., Sheba Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sheba Medical Center
ClinicalTrials.gov Identifier:
NCT01696864
Other Study ID Numbers:
  • SHEBA-12-9471-GZ-CTIL
First Posted:
Oct 1, 2012
Last Update Posted:
Jan 4, 2017
Last Verified:
Jan 1, 2017
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 4, 2017