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Wii Balance Board in Dizziness

This study has been withdrawn prior to enrollment.
(The study never started since it did not receive IRB approval)
Information provided by (Responsible Party):
Kaiser Permanente Identifier:
First received: April 28, 2011
Last updated: December 7, 2015
Last verified: December 2015
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 Intervention
Dizziness Other: Wii Balance Board

Study Type: Interventional
Study Design: 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 NLM:

Further study details as provided by Kaiser Permanente:

Enrollment: 0
Arms Assigned Interventions
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


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

Inclusion Criteria:

  • Abnormal posturography exam

Exclusion Criteria:

  • Pregnant Women and children
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01345422

Sponsors and Collaborators
Kaiser Permanente
Principal Investigator: David Cheng, MD Southern California Permanente Medical Group
  More Information

Responsible Party: Kaiser Permanente Identifier: NCT01345422     History of Changes
Other Study ID Numbers: HNS1
Study First Received: April 28, 2011
Last Updated: December 7, 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:
Sensation Disorders
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms
Vestibular Diseases
Labyrinth Diseases
Ear Diseases
Otorhinolaryngologic Diseases processed this record on September 19, 2017