UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000055528 |
|---|---|
| Receipt number | R000063451 |
| Scientific Title | Investigating the relationship between skill change and brain plasticity during sleep in patients with stroke: a cross-sectional study. |
| Date of disclosure of the study information | 2024/09/18 |
| Last modified on | 2024/09/18 10:38:20 |
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Basic information
Public title
Investigating the relationship between skill change and brain plasticity during sleep in patients with stroke: a cross-sectional study.
Acronym
Association between skill change and sleep in patients with stroke.
Scientific Title
Investigating the relationship between skill change and brain plasticity during sleep in patients with stroke: a cross-sectional study.
Scientific Title:Acronym
Association between skill change and sleep in patients with stroke.
Region
| Japan |
Condition
Condition
stroke
Classification by specialty
| Neurology | Rehabilitation medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The aim of this study is to investigate the relationship between skill change and brain plasticity during sleep in patients with stroke.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
MRI data
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
| 35 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Those who are aged 35 years and over.
Patients with stroke
Hemiplegic patients due to unilateral cerebral lesions
Healthy persons
Those who are currently healthy, have no medical conditions under treatment, and are not taking any medication (including cases where blood pressure is controlled normally with medication).
Persons with no history or experience of stroke or other neurological diseases.
Key exclusion criteria
1. Those who are unable to understand the purpose of the study owing to serious aphasia, higher brain dysfunction, or cognitive dysfunction.
2. Those who are unable to obtain written consent.
3. Those who have a diagnosis or history of psychiatric disorders.
4. Those who have a history of epileptic seizures, cardiac pacemakers, artificial heart valves, heart disease, or skin diseases.
5. Those who are habitual smokers.
6. Those who are engaged in the night shift.
7. Those who have color blindness.
8. Those who have less than 0.8 of visual acuity (including corrected vision) in both eyes.
9. Those with a habit of playing action video games or computer games.
10. Those with a diagnosis or history of sleep disorders or sleep apnea syndrome.
11. Those who score six or more on the Pittsburgh Sleep Questionnaire, six or more on the Athens Insomnia Scale, 16 or more on the CES-D or 11 or more on the Epworth Sleepiness Scale.
12. Those who take sleeping medication, anti-epileptic drugs, or other medications that affect sleep.
13. Those who do not have a regular sleep-wake routine.
14. Those who have a habit of taking naps.
15. Those who have skin sensitivity to alcohol.
16. Those who cannot wear EEG caps/electrodes.
17. Contraindications to exercise therapy.
18. Those who are currently pregnant.
19. Those who have metals in their bodies that cannot be identified as non-magnetic
20. Those with a history of temperature dysregulation, communication difficulties, or claustrophobia
21. Those who have engaged in occupations or activities where ferromagnetic materials may enter the body
22. Those who are not right-handed.
23. those who are currently participating in other experiments.
Target sample size
40
Research contact person
Name of lead principal investigator
| 1st name | Michiyuki |
| Middle name | |
| Last name | Kawakami |
Organization
Keio University
Division name
Department of Rehabilitation Medicine
Zip code
1608582
Address
35 Shinanomachi, Sinjuku-ku, Tokyo
TEL
03-5843-6169
michiyukikawakami@hotmail.com
Public contact
Name of contact person
| 1st name | Daisuke |
| Middle name | |
| Last name | Ito |
Organization
Keio University
Division name
Department of Rehabilitation Medicine
Zip code
1608582
Address
35 Shinanomachi, Sinjuku-ku, Tokyo
TEL
03-5843-6169
Homepage URL
daisuke.ito@keio.jp
Sponsor or person
Institute
Keio University
Institute
Department
Personal name
Funding Source
Organization
Japan Society for the Promotion of Science
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Japan
Other related organizations
Co-sponsor
RAIKEN
Name of secondary funder(s)
The Uehara Memorial Foundation.
IRB Contact (For public release)
Organization
Keio University
Address
35 Shinanomachi, Sinjuku-ku, Tokyo
Tel
03-5843-6169
med-rinri-jimu@adst.keio.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
| 2024 | Year | 09 | Month | 18 | 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
Open public recruiting
Date of protocol fixation
| 2024 | Year | 07 | Month | 18 | Day |
Date of IRB
| 2024 | Year | 08 | Month | 26 | Day |
Anticipated trial start date
| 2024 | Year | 09 | Month | 18 | Day |
Last follow-up date
| 2025 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Participants undergo a total of 2 MRI+PSG.
Management information
Registered date
| 2024 | Year | 09 | Month | 18 | Day |
Last modified on
| 2024 | Year | 09 | Month | 18 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063451
