UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000038690 |
|---|---|
| Receipt number | R000044099 |
| Scientific Title | Non-invasive AI wearable device for supporting medical care |
| Date of disclosure of the study information | 2019/11/25 |
| Last modified on | 2024/09/30 09:57:38 |
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Basic information
Public title
Non-invasive AI wearable device for supporting medical care
Acronym
Non-invasive AI wearable device for supporting medical care
Scientific Title
Non-invasive AI wearable device for supporting medical care
Scientific Title:Acronym
AI-supported medical care
Region
| Japan |
Condition
Condition
Epilepsy, Parkinson Disease, Cerebrovascular disease, Spinal cord injury, idiopathic normal pressure hydrocephalus, spastic paralysis
Classification by specialty
| Neurosurgery |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Development of AI system to predict unexpected events in various neurological diseases based on clinical data acquired simultaneously using non-invasive wearable device.
Basic objectives2
Others
Basic objectives -Others
prediction of unexpected events in various neurological diseases
Trial characteristics_1
Exploratory
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Relationship between clinical data and data acquired simultaneously using non-invasive wearable device
Key secondary outcomes
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
| 12 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Subjects included in this study must fulfill one of the following criteria:
1. diagnosed with Parkinson Disease or its related disease (40 to 85 years old)
2. has motor dysfunction due to cerebrovascular disease (12 years old onwards)
3. diagnosed with epilepsy (12 years old onwards)
4. diagnosed with spinal cord injury (12 years old onwards)
5. diagnosed with idiopathic normal pressure hydrocephalus (12 years old onwards)
6. diagnosed with spastic paralysis (12 years old onwards)
Key exclusion criteria
Subjects who fulfill any of the following criteria will be excluded from this study.
1. Individuals with severe intellectual disability in whom proper communication is not possible and thus wearing the wearable device deemed impossible.
2. Individuals considered incompetent to participate in this study by the attending physician.
Target sample size
300
Research contact person
Name of lead principal investigator
| 1st name | Haruhiko |
| Middle name | |
| Last name | Kishima |
Organization
Osaka University Graduate School of Medicine
Division name
Neurosurgery
Zip code
565-0871
Address
2-2, Yamadaoka, Suita, Japan.
TEL
06-6879-3652
hkishima@nsurg.med.osaka-u.ac.jp
Public contact
Name of contact person
| 1st name | Hui Ming |
| Middle name | |
| Last name | Khoo |
Organization
Osaka University Graduate School of Medicine
Division name
Neurosurgery
Zip code
565-0871
Address
2-2, Yamadaoka, Suita, Japan.
TEL
06-6879-3652
Homepage URL
khoo@nsurg.med.osaka-u.ac.jp
Sponsor or person
Institute
Osaka University
Institute
Department
Personal name
Funding Source
Organization
Cabinet Office (Japan)
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Osaka University Clinical Research Review Committee
Address
2-2, Yamadaoka, Suita
Tel
06-6210-8289
rinri@hp-crc.med.osaka-u.ac.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
| 2019 | Year | 11 | Month | 25 | 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
Enrolling by invitation
Date of protocol fixation
| 2019 | Year | 04 | Month | 24 | Day |
Date of IRB
| 2019 | Year | 10 | Month | 24 | Day |
Anticipated trial start date
| 2019 | Year | 10 | Month | 24 | Day |
Last follow-up date
| 2028 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Non-randomized non-blinded prospective case series study
Management information
Registered date
| 2019 | Year | 11 | Month | 25 | Day |
Last modified on
| 2024 | Year | 09 | Month | 30 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000044099
