UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000055444 |
|---|---|
| Receipt number | R000063311 |
| Scientific Title | Investigation for the association between reducing prolonged sedentary behavior and health outcome. |
| Date of disclosure of the study information | 2024/09/09 |
| Last modified on | 2025/09/10 15:30:52 |
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Basic information
Public title
Investigation for the association between reducing prolonged sedentary behavior and health outcome.
Acronym
Investigation for the association between reducing prolonged sedentary behavior and health outcome.
Scientific Title
Investigation for the association between reducing prolonged sedentary behavior and health outcome.
Scientific Title:Acronym
Investigation for the association between reducing prolonged sedentary behavior and health outcome.
Region
| Japan |
Condition
Condition
Not applicable
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To Investigate the association between reducing prolonged sedentary behavior and health outcome.
Basic objectives2
Others
Basic objectives -Others
To evaluate the association between reducing sedentary behavior by intervention and health outcome.
Trial characteristics_1
Exploratory
Trial characteristics_2
Developmental phase
Not applicable
Assessment
Primary outcomes
The association between reducing sedentary behavior by intervention and health outcome.
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Other |
Interventions/Control_1
Use the mobile health app for 2 weeks. Wear the accelerometers on the waist for 2 weeks before and 2 weeks after using the mobile health.
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
| 64 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
1. Male and female aged 20-64health app
2. Person who regularly wears the accelerometer and agree to provide data
3. Person who agree to wear the accelerometer
4. Person who regularly use iPhone and agree to use mobile
Key exclusion criteria
1. Person who has pain or injury that affects walking
2. Person who is difficult to walk normally due to previous surgeries, etc
Target sample size
70
Research contact person
Name of lead principal investigator
| 1st name | Tatsuya |
| Middle name | |
| Last name | Kusaura |
Organization
Kao Corporation
Division name
Human Health Care Products Research Lab.
Zip code
131-8501
Address
2-1-3, Bunka, Sumida-ku, Tokyo, 131-8501, JAPAN
TEL
+81-80-4202-2625
kusaura.tatsuya@kao.com
Public contact
Name of contact person
| 1st name | Keita |
| Middle name | |
| Last name | Kinoshita |
Organization
Kao Corporation
Division name
Human Health Care Products Research Lab.
Zip code
131-8501
Address
2-1-3, Bunka, Sumida-ku, Tokyo, 131-8501, JAPAN
TEL
+81-70-3300-8335
Homepage URL
kinoshita.keita@kao.com
Sponsor or person
Institute
Kao Corporation
Institute
Department
Personal name
Funding Source
Organization
Kao Corporation
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Human Research Ethics Committee, Kao Corporation
Address
2-1-3 Bunka, Sumida-ku, Tokyo 131-8501, JAPAN
Tel
+81-3-5630-9064
morisaki.naoko@kao.com
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 | 09 | 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
70
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
No longer recruiting
Date of protocol fixation
| 2024 | Year | 08 | Month | 29 | Day |
Date of IRB
| 2024 | Year | 08 | Month | 29 | Day |
Anticipated trial start date
| 2024 | Year | 09 | Month | 09 | Day |
Last follow-up date
| 2024 | Year | 11 | Month | 30 | 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 | 09 | Month | 06 | Day |
Last modified on
| 2025 | Year | 09 | Month | 10 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063311
