OVSCF: The Influence of Oral Vibrational Stimulation on Cognitive Function of Elderly Individuals

Sponsor
Seoul National University Bundang Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02332525
Collaborator
(none)
20
1
23

Study Details

Study Description

Brief Summary

The purpose of this study is to investigate the effect of oral vibratory stimulus on the brain activity and cognitive function of elderly people with non-dementia subjects (cognitive normal, mild cognitive impairment)

Condition or Disease Intervention/Treatment Phase
  • Device: Oral Vibrational Stimulation
Phase 1/Phase 2

Detailed Description

Evaluating the effect of oral vibratory stimulus on the brain activity and cognitive function of elderly people with mild cognitive impairment

◇ Test design: Open-labeled, prospective, pre-post study

○ Oral vibratory stimulus: As an optimal algorithm drawn through the first year study, the vibratory stimulus is applied 10 times for 15 days (a 5-minute stimulus is applied two times a day for 10 days, and it is composed of repeated 15-second vibratory and 15-second non-vibratory stimulus with a strength of 3.3V).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Influence of Oral Vibrational Stimulation on Brain Activity and Cognitive Function of Elderly Individuals With Mild Cognitive Impairment
Study Start Date :
Jan 1, 2015
Anticipated Primary Completion Date :
Dec 1, 2015
Anticipated Study Completion Date :
Dec 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

20 elders (10 mild cognitive impairment, 10 cognitive normal elders) those who received oral vibrational stimulation

Device: Oral Vibrational Stimulation
Oral application of vibratory stimulus : With the oral equipment, which is similar to the device generally used to prevent teeth grinding in dental clinics, 15-second vibratory and 15-second non-vibratory stimulus are given repeatedly for about 5 minutes using a vibrator that has a strength less than or equal to the vibratory stimulus of a smartphone (3.3V, 166Hz, maximum 180Hz). A stimulus of two times for 5 minutes, a total of at least 10 minutes is conducted for 10 days in a hospital or designated place.

Outcome Measures

Primary Outcome Measures

  1. cognitive function [15 days]

    Cambridge Neuropsychological Test Automated Battery (CANTAB, Cambridge Cognition, Cambridge, United Kingdom) (Sahgal, et al., 1992; Blackwell, et al., 2004; O'Connell, et al., 2004; Junkkila, Oja, Laine, & Karrasch, 2012) Paired Associates Learning (PAL) : Memory function Spatial Working Memory (SWM): frontal-executive function Stockings Of Cambridge (SOC): spatial planning ability and problem-solving ability

Secondary Outcome Measures

  1. quantitative electroencephalography (QEEG) and event-related potentials (ERPs) [15 days]

    : Based on a significant reduction of the relative power of α-wave (8-13Hz) and significant increase of the relative power of β-wave (13-30Hz) - Short-term and long-term ERP changes caused by oral vibratory stimulus: Change of amplitude and latency period of P300, the ERP component related to attention

  2. functional magnetic resonance imaging (fMRI) [15 days]

    Assessing what difference the activated areas show compared to the results of the previous studies that identified the activated parts after masticatory activities when only oral vibratory stimulus is given without masticatory activities

  3. masticatory ability [15 days]

    Unilateral maximal bite force is measured with a simple bite force gauge with a stick form (GM 10 occlusal force-meter: Nagano Keiki C., LTD, Japan). This is measured three times in a place where the subject feels at ease. Maximum bite force: Numeric difference before and after the application of vibratory stimulus Evaluation of masticatory ability: The change of Shape and color difference ofin gum before and after the application of vibratory stimulus

  4. salivary secretion [15 days]

    Evaluation of salivary secretion amount: mL per unit time (min) of saliva collected before and after the application of vibratory stimulus Evaluation of compliance: The measurement of Tthe number of performances ofperforming the oral vibratory stimulus for 15 days for two times/day

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Inclusion Criteria

  • A person who has at least 20 natural teeth, including the first molars (including fixed prostheses and implants, excluding removable prostheses)

  • A person who has systemic health, including controlled hypertension/hypotension and diabetes patients

  • An elderly person who has been diagnosed with normal cognition or mild cognitive impairment in a neuropsychological test and CERAD clinical evaluation (refer to separate inclusion criteria)

Exclusion Criteria

  • A person who has medical history of nervous system disease

  • A person who is has ever been allergic to resin

  • A person who has untreated periodontal disease and/or severely loose teeth

  • A person who has a medical treatment history of temporomandibular disorders, who has an occurrence of stomatitis once or more per month within the last 6 months, or who currently has stomatitis

  • A person who is receiving or has received treatment for major mental diseases such as dementia, major depression, or mania based on the DSM-IV diagnosis

  • A person who has a medical disease that can have a serious effect on cognitive function or is taking related medicine

  • A person who has a transplant that is electrically or mechanically operated or a cerebrovascular clip or who has claustrophobia so that an MRI scan is impossible

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Seoul National University Bundang Hospital

Investigators

  • Principal Investigator: Hyo-Jung Lee, Seoul National University Bundang Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Lee, Hyo-Jung, assistant professor, Seoul National University Bundang Hospital
ClinicalTrials.gov Identifier:
NCT02332525
Other Study ID Numbers:
  • B-1407-260-006
First Posted:
Jan 6, 2015
Last Update Posted:
Jan 6, 2015
Last Verified:
Jan 1, 2015
Keywords provided by Lee, Hyo-Jung, assistant professor, Seoul National University Bundang Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 6, 2015