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Microsoft Kinect, Gait Function,Hemineglect, Vestibulo-ocular Training

Primary Purpose

Hemiplegic Gait

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
vestibuloocular training
regular exercise training for hemiplegic patients
Sponsored by
Beni-Suef University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemiplegic Gait

Eligibility Criteria

60 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subjects age will range from (60-70) years old.
  • Patients who had a stroke at least six months prior.
  • Patients who had visual field defects post stroke.
  • Patients who could walk without caretaker assistance or no severe dyskinesias.
  • Adequate hearing (hearing aid if required).
  • Patients who had no problem with their state of consciousness and absence of dementia
  • Patients who had no orthopedic problems that may affect gait.
  • Patients will be chosen in both sexes.
  • Clinically and medically stable.

Exclusion Criteria:

Patients who will meet one of the following criteria will be excluded from the study:

  • Only one functional eye.
  • Neurological problem or any severe co-morbidity likely to affect gait.
  • Intact visual field.
  • Instability of patient's medical condition.
  • Obese ( BMI ≥ 30 Kg∕m2 ).
  • Association with another medical problem that can affect patient

Sites / Locations

  • Beni Suef University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

study group

control group

Arm Description

20 patient with hemineglect, minimum 6 months post stroke

20 patient with hemineglect, minimum 6 months post stroke

Outcomes

Primary Outcome Measures

gait changes in hemineglect patient after vestibulo ocular rehabilitation program
gait assesment using microsoft kinect for hemineglect patient pre and post vestibulo ocular rehabilitation

Secondary Outcome Measures

Full Information

First Posted
April 9, 2019
Last Updated
July 23, 2019
Sponsor
Beni-Suef University
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1. Study Identification

Unique Protocol Identification Number
NCT03913663
Brief Title
Microsoft Kinect, Gait Function,Hemineglect, Vestibulo-ocular Training
Official Title
A Model Based Study for Gait in Heminglect Patient Pre and Post Vestibul-ocular Rehabilitation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
May 22, 2019 (Actual)
Primary Completion Date
July 15, 2019 (Actual)
Study Completion Date
July 18, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beni-Suef University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Gait problems in hemineglect patient post stroke , vestibuloocular training plays a role in improving gait function, gait assessment using a model based study (Microsoft Kinect) for pre and post training assesment.
Detailed Description
The syndrome of visuospatial neglect is a common consequence of unilateral brain injury. It is most often associated with stroke and is more severe and persistent following right hemisphere damage, with reported frequencies in the acute stage of up to 80%. This may result in gait disturbance, high levels of energy expenditure and increase the risk of falls. Vestibuleo-ocular training techniques are aimed at improving or even restoring visual function by training patients to detect stimuli in the blind hemifield and increase their overall sensitivity to them. The investigators propose a model based (Microsoft Kinect), a device can be used for assessment of spatiotemporal gait variables as well as gait kinematics.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemiplegic Gait

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
study group
Arm Type
Active Comparator
Arm Description
20 patient with hemineglect, minimum 6 months post stroke
Arm Title
control group
Arm Type
Active Comparator
Arm Description
20 patient with hemineglect, minimum 6 months post stroke
Intervention Type
Other
Intervention Name(s)
vestibuloocular training
Other Intervention Name(s)
regular exercise training for hemiplegic patients
Intervention Description
using vestibulo ocular training program for training neglect patient
Intervention Type
Other
Intervention Name(s)
regular exercise training for hemiplegic patients
Intervention Description
Traditional gait training program.
Primary Outcome Measure Information:
Title
gait changes in hemineglect patient after vestibulo ocular rehabilitation program
Description
gait assesment using microsoft kinect for hemineglect patient pre and post vestibulo ocular rehabilitation
Time Frame
baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects age will range from (60-70) years old. Patients who had a stroke at least six months prior. Patients who had visual field defects post stroke. Patients who could walk without caretaker assistance or no severe dyskinesias. Adequate hearing (hearing aid if required). Patients who had no problem with their state of consciousness and absence of dementia Patients who had no orthopedic problems that may affect gait. Patients will be chosen in both sexes. Clinically and medically stable. Exclusion Criteria: Patients who will meet one of the following criteria will be excluded from the study: Only one functional eye. Neurological problem or any severe co-morbidity likely to affect gait. Intact visual field. Instability of patient's medical condition. Obese ( BMI ≥ 30 Kg∕m2 ). Association with another medical problem that can affect patient
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
mohammed elhamrawy, master
Organizational Affiliation
Beni-Suef University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beni Suef University
City
Banī Suwayf
State/Province
Beni Suef
ZIP/Postal Code
62511
Country
Egypt

12. IPD Sharing Statement

Citations:
PubMed Identifier
28767091
Citation
Gambi E, Agostinelli A, Belli A, Burattini L, Cippitelli E, Fioretti S, Pierleoni P, Ricciuti M, Sbrollini A, Spinsante S. Heart Rate Detection Using Microsoft Kinect: Validation and Comparison to Wearable Devices. Sensors (Basel). 2017 Aug 2;17(8):1776. doi: 10.3390/s17081776.
Results Reference
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PubMed Identifier
28980076
Citation
Basagni B, De Tanti A, Damora A, Abbruzzese L, Varalta V, Antonucci G, Bickerton WL, Smania N, Mancuso M. The assessment of hemineglect syndrome with cancellation tasks: a comparison between the Bells test and the Apples test. Neurol Sci. 2017 Dec;38(12):2171-2176. doi: 10.1007/s10072-017-3139-7. Epub 2017 Oct 4.
Results Reference
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PubMed Identifier
30251187
Citation
Muntaseer Mahfuz M, Schubert MC, Figtree WVC, Todd CJ, Migliaccio AA. Human Vestibulo-Ocular Reflex Adaptation Training: Time Beats Quantity. J Assoc Res Otolaryngol. 2018 Dec;19(6):729-739. doi: 10.1007/s10162-018-00689-w. Epub 2018 Sep 24.
Results Reference
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Microsoft Kinect, Gait Function,Hemineglect, Vestibulo-ocular Training

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