Effects of Whole-body Vibration Exercise in Brain Injury Patients With Minimally Conscious State

Sponsor
Samsung Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT03389113
Collaborator
(none)
10
1
2
47.9
0.2

Study Details

Study Description

Brief Summary

The purpose of this study is to investigate the effect of the whole body vibration exercise on cortical activity and consciousness Level in brain injury patients with minimally conscious state.

Condition or Disease Intervention/Treatment Phase
  • Device: Whole body vibration
  • Other: Exersice
N/A

Detailed Description

Whole body vibration exercise can provide proper somatosensory stimulation and improve muscle strength and postural control. However, there has not yet been a report on the cortical activity changes induced by whole body vibration exercise in brain injury patients with minimally conscious state.

Patients will be randomly assigned to one of the two groups. One group will go through whole body vibration with exercise and the other will only perform exercise. The primary outcome measurement of this study was cerebral cortex activity based on changes in oxygenated hemoglobin concentration using functional near-infrared spectroscopy. Behavioral assessment were performed using the coma recovery scale-revised and modified ashworth scale.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Eligible patients were randomly assigned to one of the two groups in a 1:1 ratio using an odd or even random numbers table. Whole body vibration group performed five sessions of whole body vibration exercise via a vibrating platform (Galileo® Advanced Plus, Novotec Medical, Pforzheim, Germany) with a magnitude of 20 Hz and an amplitude of 4 mm. The control group performed the same sessions without vibration.Eligible patients were randomly assigned to one of the two groups in a 1:1 ratio using an odd or even random numbers table. Whole body vibration group performed five sessions of whole body vibration exercise via a vibrating platform (Galileo® Advanced Plus, Novotec Medical, Pforzheim, Germany) with a magnitude of 20 Hz and an amplitude of 4 mm. The control group performed the same sessions without vibration.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effects of Whole-body Vibration Exercise on Cortical Activity and Consciousness Level in Brain Injury Patients With Minimally Conscious State: Pilot Study
Actual Study Start Date :
Jan 2, 2017
Anticipated Primary Completion Date :
Dec 31, 2020
Anticipated Study Completion Date :
Dec 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Whole body vibration group

Whole body vibration group performed five sessions of whole body vibration exercise via a vibrating platform (Galileo® Advanced Plus, Novotec Medical, Pforzheim, Germany) with a magnitude of 20 Hz and an amplitude of 4 mm.

Device: Whole body vibration
Whole body vibration exercise is a stimulus that uses vibrations generated on a machine with oscillatory movement determined by the amplitude and frequency of the vibration.

Other: Exersice
Exercise maintain a half-squat position (knee joint angle at 160 degrees) on the tilt table with an incline of 60 degrees.

Active Comparator: Exercise only group

The control group performed the same session without vibration.

Other: Exersice
Exercise maintain a half-squat position (knee joint angle at 160 degrees) on the tilt table with an incline of 60 degrees.

Outcome Measures

Primary Outcome Measures

  1. Cerebral cortex activity [session 0 (initial visit); session 6 (at approximately 6 days); at 2 weeks (follow-up)]

    Cerebral cortex activity was measured based on changes in oxygenated hemoglobin concentration using fNIRS

Secondary Outcome Measures

  1. Coma Recovery Scale-Revised [session 0 (initial visit); session 6 (at approximately 6 days); at 2 weeks (follow-up)]

    assess patients with a disorder of consciousness, commonly coma The CRS-R consists of 23 items, grouped into 6 sub-scales: .Auditory Visual Motor Oromotor Communication Arousal The lowest score on each sub-scale represents reflexive activity; the highest represents behaviors mediated by cognitive input. The total score ranges between 0 (worst) and 23 (best). This measure takes a minimum of 25 minutes to complete.

  2. Modified Ashworth scale [session 0 (initial visit); session 6 (at approximately 6 days); at 2 weeks (follow-up)]

    measures resistance during passive soft-tissue stretching and is used as a simple measure of spasticity The Ashworth scale is one of the most widely used methods of measuring spasticity, due in a large part to the simplicity and reproducible method. 0: No increase in muscle tone Grade Description Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved Considerable increase in muscle tone, passive movement difficult Affected part(s) rigid in flexion or extension

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients whose consciousness level was assessed as minimally conscious state by traumatic brain injury, stroke, and hypoxic brain injury

  • Patients who had more than 3 months after brain injury

Exclusion Criteria:
  • Patients under 18 years of age and older patients over 80 years

  • Pregnant women

  • In cases of uncontrolled internal or external disease

  • Patients with severe heart, musculoskeletal problems and disabilities, and those with severe neurological lesions prior to brain injury

  • Acute or chronic venous thrombosis or hemorrhage

  • Person wearing an implant on the spine

  • People with severe osteoporosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsung Medical Center Seoul Korea, Republic of

Sponsors and Collaborators

  • Samsung Medical Center

Investigators

  • Principal Investigator: Yun-Hee Kim, MD, PhD, Samsung Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Samsung Medical Center
ClinicalTrials.gov Identifier:
NCT03389113
Other Study ID Numbers:
  • 2016-04-101-004
First Posted:
Jan 3, 2018
Last Update Posted:
Sep 20, 2019
Last Verified:
Dec 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 20, 2019