UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000063389 |
|---|---|
| Receipt number | R000072451 |
| Scientific Title | Shopping data-based Individualized Recommendations for nUtrition and Health: SIRU+ Tama Study |
| Date of disclosure of the study information | 2026/10/25 |
| Last modified on | 2026/10/23 16:57:22 |
* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments
Basic information
Public title
Shopping data-based Individualized Recommendations for nUtrition and Health: SIRU+ Tama Study
Acronym
Shopping data-based Individualized Recommendations for nUtrition and Health: SIRU+ Tama Study
Scientific Title
Shopping data-based Individualized Recommendations for nUtrition and Health: SIRU+ Tama Study
Scientific Title:Acronym
SIRU+ Tama Study
Region
| Japan |
Condition
Condition
Older adults
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
This study aims to introduce SIRU+, a digital nutrition support service that uses purchasing data from everyday shopping, among older adults in Mitaka City, Tokyo, and to explore its implementation feasibility and effects on dietary habits and health promotion.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Reach
Effectiveness
Adoption
Implementation
Maintenance
Key secondary outcomes
Nutrition and dietary habits: Nutrient adequacy and deficiency trends, nutritional balance, and undernutrition
Purchasing behavior and patterns: Purchasing trends by food category, diversity of purchases, and reliance on a fixed set of products
Health and higher cognitive functions: Purchasing patterns and cognitive function
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
| 65 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Residents of Mitaka City
Aged 65 years or older at the time of informed consent
Individuals who have provided written informed consent to participate in this study
Key exclusion criteria
Individuals certified as requiring long-term care at levels 1-5 under Japan Long-Term Care Insurance system
Individuals otherwise deemed unsuitable for participation by the principal investigator
Target sample size
30
Research contact person
Name of lead principal investigator
| 1st name | Naoki |
| Middle name | |
| Last name | Sakane |
Organization
National Hospital Organization Kyoto Medical Center
Division name
Clinical Research Institute
Zip code
6128555
Address
1-1 Mukaihata-cho, Fushimi-ku, Kyoto
TEL
0756419161
404-j-doit1@mail.hosp.go.jp
Public contact
Name of contact person
| 1st name | Akiko |
| Middle name | |
| Last name | Suganuma |
Organization
National Hospital Organization Kyoto Medical Center
Division name
Clinical Research Institute
Zip code
6128555
Address
1-1 Mukaihata-cho, Fushimi-ku, Kyoto
TEL
0756419161
Homepage URL
404-j-doit1@mail.hosp.go.jp
Sponsor or person
Institute
National Hospital Organization Kyoto Medical Center
Institute
Department
Personal name
AKIKO SUGANUMA
Funding Source
Organization
KAKENHI
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
National Hospital Organization Kyoto Medical Center
Address
1-1 Mukaihata-cho, Fushimi-ku, Kyoto
Tel
0756419161
jjddooiitt11@yahoo.co.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
| 2026 | Year | 10 | 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
Preinitiation
Date of protocol fixation
| 2026 | Year | 10 | Month | 19 | Day |
Date of IRB
Anticipated trial start date
| 2026 | Year | 11 | Month | 01 | 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
Implementation study
Management information
Registered date
| 2026 | Year | 10 | Month | 23 | Day |
Last modified on
| 2026 | Year | 10 | Month | 23 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000072451
