UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000056468 |
|---|---|
| Receipt number | R000064530 |
| Scientific Title | Effects of Deep Micro Vibrotactile (DMV) on stress. |
| Date of disclosure of the study information | 2025/01/01 |
| Last modified on | 2026/04/30 13:39:20 |
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Basic information
Public title
Effects of Deep Micro Vibrotactile (DMV) on stress.
Acronym
Effects of Deep Micro Vibrotactile (DMV) on stress.
Scientific Title
Effects of Deep Micro Vibrotactile (DMV) on stress.
Scientific Title:Acronym
Effects of Deep Micro Vibrotactile (DMV) on stress.
Region
| Japan |
Condition
Condition
Residents of pay homes or serviced housing for the elderly
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To ascertain the effects of Deep Micro Vibrotactile (DMV) on stress in residents of a private or serviced retirement home.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Changes resulting from assessment using the Japanese version of POMS2 (TMD, TA, DD, AH, VA, FI, CB, F).
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Single blind -participants are blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Other |
Interventions/Control_1
Deep Micro Vibrotactile
Interventions/Control_2
without treatment
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
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
(i) Those who are currently residing in a fee-based nursing home or a serviced accommodation for the elderly.
(ii) Those who are able to lead a normal life during the test period
(iii) Those who can obtain written consent of their own free will.
Key exclusion criteria
(i) Those diagnosed with dementia.
(ii) Those with circadian rhythm disorder
(iii) Those with a history of psychiatric disorders or with psychiatric disorders
(iv) Those who regularly use antipsychotics, antidepressants or other medicines that may affect this clinical study
(v) Those with alcohol or drug abuse
(vi) Those with serious complications
(vii) Those who are participating in other clinical trials or have participated in other clinical trials within the past month
(viii) Other persons who are deemed unsuitable by the principal investigator or research assistant.
Target sample size
36
Research contact person
Name of lead principal investigator
| 1st name | keiji |
| Middle name | |
| Last name | inoue |
Organization
Kochi Medical School Hospital
Division name
Center for Next Generation Medical Research
Zip code
783-8505
Address
kohasu, okou Town, Nankoku City, Kochi Prefecture
TEL
088-880-2719
keiji@kochi-u.ac.jp
Public contact
Name of contact person
| 1st name | Hiroko |
| Middle name | |
| Last name | Iijima |
Organization
Kochi Medical School Hospital
Division name
Center for Next Generation Medical Research
Zip code
783-8505
Address
kohasu, okou Town, Nankoku City, Kochi Prefecture
TEL
088-880-2719
Homepage URL
h.iijima@kochi-u.ac.jp
Sponsor or person
Institute
Kochi Medical School Hospital
Institute
Department
Personal name
Funding Source
Organization
self-procurement
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Kochi Medical School Hospital
Address
kohasu, okou Town, Nankoku City, Kochi Prefecture
Tel
0888-80-2180
rinri21@kochi-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
| 2025 | Year | 01 | Month | 01 | 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
| 2024 | Year | 11 | Month | 17 | Day |
Date of IRB
| 2024 | Year | 12 | Month | 06 | Day |
Anticipated trial start date
| 2025 | Year | 02 | Month | 01 | Day |
Last follow-up date
| 2025 | Year | 08 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2024 | Year | 12 | Month | 16 | Day |
Last modified on
| 2026 | Year | 04 | Month | 30 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064530
