UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000041284 |
|---|---|
| Receipt number | R000047149 |
| Scientific Title | Effect of motion illusion induced by vibration stimulator on motor function - prospective observational study - |
| Date of disclosure of the study information | 2020/08/24 |
| Last modified on | 2025/02/05 10:01:04 |
* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments
Basic information
Public title
Effect of motion illusion induced by vibration stimulator on motor function - prospective observational study -
Acronym
Effect of motion illusion induced by vibration stimulator on motor function - prospective observational study -
Scientific Title
Effect of motion illusion induced by vibration stimulator on motor function - prospective observational study -
Scientific Title:Acronym
Effect of motion illusion induced by vibration stimulator on motor function - prospective observational study -
Region
| Japan |
Condition
Condition
Stroke
Classification by specialty
| Neurology | Rehabilitation medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To investigate whether motor function recovery is enhanced by motion illusions.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Exploratory
Trial characteristics_2
Explanatory
Developmental phase
Not applicable
Assessment
Primary outcomes
Changes of the clinical scores after the 2-week intervention.
(Motor paralysis)
Fugl-Meyer Assessment
Key secondary outcomes
Changes of the clinical scores after the 2-week intervention.
(Upper limb function)
ARAT: Action Research Assessment Test, BBT: Box and Block Test
(Lower limb function)
BBS: Berg Balance Scale, 10MWT: 10m Walking Test
(Activities of daily living)
FIM: Functional Independence Measure
(Cutaneous sensation)
SWT: Semmes Weinstein Monofilament
(Proprioceptive sensation)
Number of correct answers
(Muscle tone)
MAS: Modified Ashworth Scale
(Subjective evaluation)
Product Trial Feedback Sheet
Base
Study type
Observational
Study design
Basic design
Randomization
Randomization unit
Blinding
Control
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
Purpose of intervention
Type of intervention
Interventions/Control_1
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 20 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Hemiparetic patients after stroke
Key exclusion criteria
Dementia(MMSE<23), severe aphasia, severe sensory disturbance or pain, contracture of the upper extremity
Target sample size
20
Research contact person
Name of lead principal investigator
| 1st name | Ichiro |
| Middle name | |
| Last name | Miyai |
Organization
Morinomiya hospital
Division name
Neurorehabilitation Research Institute
Zip code
5360025
Address
2-1-88 Morinomiya, Joto-ku, Osaka City, Osaka, Japan
TEL
06-6969-0111
miyai@omichikai.or.jp
Public contact
Name of contact person
| 1st name | Misako |
| Middle name | |
| Last name | Miyata |
Organization
Morinomiya Hospital
Division name
Officer
Zip code
5360025
Address
2-1-88 Morinomiya, Joto-ku, Osaka City, Osaka, Japan
TEL
06-6969-0111
Homepage URL
miyata@omichikai.or.jp
Sponsor or person
Institute
Morinomiy Hospital
Institute
Department
Personal name
Funding Source
Organization
Sakai Medical Corporation
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Japan
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Omichi-kai Social Medical Corporation IRB
Address
2-1-88 Morinomiya, Joto-ku, Osaka City, Osaka, Japan
Tel
06-6969-0111
nrri-jimu@omichikai.or.jp
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2020 | Year | 08 | Month | 24 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Completed
Date of protocol fixation
| 2020 | Year | 08 | Month | 24 | Day |
Date of IRB
| 2020 | Year | 08 | Month | 19 | Day |
Anticipated trial start date
| 2020 | Year | 08 | Month | 24 | Day |
Last follow-up date
| 2021 | Year | 08 | Month | 24 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
None
Management information
Registered date
| 2020 | Year | 08 | Month | 03 | Day |
Last modified on
| 2025 | Year | 02 | Month | 05 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000047149
