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Virtual Reality in Motor Performance and Quality of Life in Patients With Parkinson's Disease

Primary Purpose

Parkinson Disease

Status
Completed
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
treatment with Nintendo wii.
Physical therapy conventional.
Sponsored by
Federal University of Bahia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease focused on measuring Parkinson's disease, Physical therapy, Virtual Reality, Quality of life, Motor performance

Eligibility Criteria

50 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Clinical diagnosis of Parkinson's disease
  • Both the sex with age between 50 and 80 years
  • To be in it I serve as apprentice of 1 the 3,0 in the scale of Hoehn Yahr

Exclusion Criteria:

  • Cognitive impairment
  • Poorly controlled arterial hypertension
  • Poorly controlled Cardiopathy

Sites / Locations

  • Ambulatorio Magalhães Neto

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Treatment group - Nintendo wii.

conventional - Physical Therapy

Arm Description

Outcomes

Primary Outcome Measures

Quality of life
Parkinson's disease questionnaire (PDQ-39)
Motor performance
the Unified Parkinson's Disease Rating Scale (UPDRS.)

Secondary Outcome Measures

Full Information

First Posted
May 10, 2010
Last Updated
December 6, 2011
Sponsor
Federal University of Bahia
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1. Study Identification

Unique Protocol Identification Number
NCT01120392
Brief Title
Virtual Reality in Motor Performance and Quality of Life in Patients With Parkinson's Disease
Official Title
Virtual Reality in Motor Performance and Quality of Life in Patients With Parkinson's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
December 2011
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
October 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of Bahia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Treatment with Nintendo wii is higher to physical therapy conventional in the quality of life and motor performance in patients with Parkinson's disease.
Detailed Description
The aim of this study is to assess if the treatment of rehabilitation with Nintendo wii is higher to the conventional in the quality of life and motor performance in patients with Parkinson's disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Parkinson's disease, Physical therapy, Virtual Reality, Quality of life, Motor performance

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment group - Nintendo wii.
Arm Type
Experimental
Arm Title
conventional - Physical Therapy
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
treatment with Nintendo wii.
Intervention Description
Participants Will receive treatment with Nintendo Wii over one months. These Patients Will Be subjected to mobilization of stem and stretching. Then Will Be Submitted to Nintendo wii games. Will Be Submitted This group three times a week to a treatment protocol with boxing exercises with wii sports and wii fit
Intervention Type
Other
Intervention Name(s)
Physical therapy conventional.
Intervention Description
Conventional exercises used with the same goals for the group with wii
Primary Outcome Measure Information:
Title
Quality of life
Description
Parkinson's disease questionnaire (PDQ-39)
Time Frame
4 weeks (Baseline and after four weeks)
Title
Motor performance
Description
the Unified Parkinson's Disease Rating Scale (UPDRS.)
Time Frame
4 weeks (Baseline and after four weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of Parkinson's disease Both the sex with age between 50 and 80 years To be in it I serve as apprentice of 1 the 3,0 in the scale of Hoehn Yahr Exclusion Criteria: Cognitive impairment Poorly controlled arterial hypertension Poorly controlled Cardiopathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ailton Melo, PhD
Organizational Affiliation
UFBA- DINEP
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ambulatorio Magalhães Neto
City
Salvador
State/Province
Bahia
Country
Brazil

12. IPD Sharing Statement

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