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Wii Balance Board in Dizziness

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ClinicalTrials.gov Identifier: NCT01345422
Recruitment Status : Withdrawn (The study never started since it did not receive IRB approval)
First Posted : May 2, 2011
Last Update Posted : December 9, 2015
Sponsor:
Information provided by (Responsible Party):
Kaiser Permanente

Study Description
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Brief Summary:
Patients with dizziness presently undergo physical therapy rehabilitation. Our study will study whether Wii Balance Board made by Nintendo Inc. will be helpful in patients with dizziness. They will undergo dizziness evaluation to quantify their dizziness.

Condition or disease Intervention/treatment Phase
Dizziness Other: Wii Balance Board Not Applicable

Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: A Pilot Study to Assess the Usefulness of the Wii Balance Board for Dizziness

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Arms and Interventions
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Arm Intervention/treatment
Experimental: Wii Balance Board
Wii Balance Board Training
 Other: Wii Balance Board
Participant will undergo Nintendo Wii Balance Board training for two months , five days a week for 30 minutes


Outcome Measures
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Eligibility Criteria
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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Abnormal posturography exam

Exclusion Criteria:

  • Pregnant Women and children
Contacts and Locations
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01345422


Sponsors and Collaborators
Kaiser Permanente
Investigators
Principal Investigator: David Cheng, MD Southern California Permanente Medical Group
More Information
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Responsible Party: Kaiser Permanente
ClinicalTrials.gov Identifier: NCT01345422     History of Changes
Other Study ID Numbers: HNS1
First Posted: May 2, 2011    Key Record Dates
Last Update Posted: December 9, 2015
Last Verified: December 2015
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: this study did not receive IRB approval

Additional relevant MeSH terms:
Dizziness
Vertigo
Sensation Disorders
Neurologic Manifestations
Nervous System Diseases
 Signs and Symptoms
Vestibular Diseases
Labyrinth Diseases
Ear Diseases
Otorhinolaryngologic Diseases