Vestibular Rehabilitation and Dizziness in Geriatric Patients
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
|Official Title:||Vestibular Rehabilitation and Dizziness in Geriatric Patients|
- Dynamic Gait Index [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]Fall risk was determined using the Dynamic Gait Index (DGI). A maximum total score of 24 is possible and a total score of < 20 indicates risk for falling.
- Dynamic Visual Acuity [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]Visual acuity during head movement (dynamic visual acuity, DVA) was measured using customized computerized software. DVA is measured in Logarithm of the Minimum Angle of Resolution (LogMAR). Participants identified letters while turning the head from side to side between 120 and 180 deg/s. DVA, the difference in acuity between head stationary and moving, is reported as the average of rightward and leftward scores; higher scores indicate worse visual acuity.
|Study Start Date:||April 2006|
|Study Completion Date:||August 2009|
|Primary Completion Date:||August 2009 (Final data collection date for primary outcome measure)|
Experimental: Vestibular Rehabilitation
vestibular exercises plus standard balance and gait exercises
Behavioral: Vestibular rehabilitation
vestibular adaptation and substitution exercises
Placebo Comparator: Placebo
placebo exercises plus standard balance and gait exercises
placebo vestibular exercises
Community dwelling older individuals who present to a specialty dizziness clinic (Atlanta VAMC or Emory University) with a primary complaint of dizziness will be recruited to participate in this study. Before beginning the study, the presence of normal vestibular function will be measured directly using standard vestibular function tests. Individuals will be randomly assigned to the vestibular exercise group (VR) or to the control group (CON). Data will be collected prior to the initiation of physical therapy and at the completion of the 6-week intervention period.
The VR group will perform vestibular exercises plus balance and gait exercises. The CON group will perform saccadic eye movements without targets against a blank wall, as well as balance and gait exercises. The balance and gait exercises for each group will be based on identified impairments and functional limitations, as is the standard of care in physical therapy. All subjects within a group will follow the same exercise progression for the vestibular or eye movement exercises. Subjects will be seen in the clinic on a weekly basis to review and modify the exercises according to a standard protocol and to reinforce compliance.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00275392
|United States, Georgia|
|Atlanta VA Medical and Rehab Center, Decatur|
|Decatur, Georgia, United States, 30033|
|Principal Investigator:||Courtney D. Hall, PhD PT||Mountain Home VA Medical Center James H. Quillen VA Medical Center, Mountain Home, TN|