UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000035256 |
|---|---|
| Receipt number | R000039682 |
| Scientific Title | Development of Healthy Walking Support System based on AI-based auto-recommendation System and Gamification |
| Date of disclosure of the study information | 2019/01/31 |
| Last modified on | 2023/06/19 20:09:45 |
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Basic information
Public title
Development of Healthy Walking Support System based on AI-based auto-recommendation System and Gamification
Acronym
Healthy Waking Support System
Scientific Title
Development of Healthy Walking Support System based on AI-based auto-recommendation System and Gamification
Scientific Title:Acronym
Healthy Waking Support System
Region
| Japan |
Condition
Condition
none
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To seek Effective Recommendation (contents / timing) to arouse health promoting activity.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Number of stems, Amount of activity (Mets, calorie consumption)
Key secondary outcomes
Subjective opinion on given recommendations
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
Educational,Counseling,Training
Type of intervention
| Behavior,custom |
Interventions/Control_1
Automatic Recommendation
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
| 70 | years-old | > |
Gender
Male and Female
Key inclusion criteria
The ones who provide written consent under ones own will after having sufficient explanation about the test
Key exclusion criteria
1) The ones with disease including life-style disease
2) The ones who doesn't provide written consent
3) The ones who are judged inappropriate as the subject by the research director
Target sample size
50
Research contact person
Name of lead principal investigator
| 1st name | Tomohiro |
| Middle name | |
| Last name | Kuroda |
Organization
Kyoto University Hospital
Division name
Division of Medical IT and Admin. Plan.
Zip code
606-8507
Address
Shogo-in Kawahara-cho 54, Sakyo, Kyoto, Japan
TEL
075-366-7701
medinfoq@kuhp.kyoto-u.ac.jp
Public contact
Name of contact person
| 1st name | Tomohiro |
| Middle name | |
| Last name | Kuroda |
Organization
Kyoto University Hospital
Division name
Division of Medical IT and Admin plan
Zip code
606-8507
Address
Shogo-in Kawahara-cho 54, Sakyo, Kyoto, Japan
TEL
075-366-7701
Homepage URL
medinfoq@kuhp.kyoto-u.ac.jp
Sponsor or person
Institute
Kyoto University Hospital
Institute
Department
Personal name
Funding Source
Organization
Platinum Data Science Co.
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
Kyoto University Graduate School and Faculty of Medicine, Ethics Committee
Address
Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, JAPAN
Tel
075-753-4680
ethcom@kuhp.kyoto-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 | 01 | Month | 31 | 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
Preinitiation
Date of protocol fixation
| 2018 | Year | 12 | Month | 07 | Day |
Date of IRB
Anticipated trial start date
| 2018 | Year | 12 | Month | 21 | Day |
Last follow-up date
| 2023 | Year | 06 | 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
| 2018 | Year | 12 | Month | 14 | Day |
Last modified on
| 2023 | Year | 06 | Month | 19 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000039682
| Research Plan | |
|---|---|
| Registered date | File name |
| Research case data specifications | |
|---|---|
| Registered date | File name |
| Research case data | |
|---|---|
| Registered date | File name |
