UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000059182 |
|---|---|
| Receipt number | R000067693 |
| Scientific Title | A Survey on Adherence to Nutritional Supplements among Community-Dwelling Older Adults |
| Date of disclosure of the study information | 2025/10/14 |
| Last modified on | 2025/10/14 14:53:04 |
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Basic information
Public title
A Survey on Adherence to Nutritional Supplements among Community-Dwelling Older Adults
Acronym
A Survey on Adherence to Nutritional Supplements
Scientific Title
A Survey on Adherence to Nutritional Supplements among Community-Dwelling Older Adults
Scientific Title:Acronym
A Survey on Adherence to Nutritional Supplements
Region
| Japan |
Condition
Condition
Older Adults in Need of Nutritional Intervention
Classification by specialty
| Not applicable |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
This study aims to examine adherence to nutritional supplements and explore strategies for improving nutritional support among community-dwelling older adults.
Basic objectives2
Safety
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Adherence to Nutritional Supplements
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
| 65 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
1) Men and women aged 65 years or older
2) Individuals certified as requiring long-term care or support
3) Not currently hospitalized or residing in a long-term care facility
4) Currently taking prescribed nutritional supplements at the time of completing the questionnaire
5) Able to fully understand the study details and provide voluntary informed consent to participate
Key exclusion criteria
None
Target sample size
200
Research contact person
Name of lead principal investigator
| 1st name | Yukikazu |
| Middle name | |
| Last name | Kamada |
Organization
Nestle Japan Ltd
Division name
Nestle Health Science Company
Zip code
140-0002
Address
Tennozu Ocean Square 20F, 2-2-20 Higashi-Shinagawa, Shinagawa-ku, Tokyo
TEL
070-2278-7597
Yukikazu.Kamada@jp.nestle.com
Public contact
Name of contact person
| 1st name | Hiroki |
| Middle name | |
| Last name | Takano |
Organization
Nestle Japan Ltd
Division name
Nestle Health Science Company
Zip code
140-0002
Address
Tennozu Ocean Square 20F, 2-2-20 Higashi-Shinagawa, Shinagawa-ku, Tokyo
TEL
070-2448-5234
Homepage URL
hiroki.takano@jp.nestle.com
Sponsor or person
Institute
Nestle Health Science Company
Institute
Department
Personal name
Funding Source
Organization
Nestle Japan Ltd
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
Shiba Palace Clinic Ethics Review Committee
Address
aiwaA Hamamatsucho Bldg. 6F, 1-9-10, Hamamatsucho, Minato-ku, Tokyo, Japan
Tel
03-5408-1599
shiba_palace@s-palace-clinic.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
| 2025 | Year | 10 | Month | 14 | 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
200
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
| 2025 | Year | 09 | Month | 24 | Day |
Date of IRB
| 2025 | Year | 09 | Month | 25 | Day |
Anticipated trial start date
| 2025 | Year | 09 | Month | 26 | Day |
Last follow-up date
| 2025 | Year | 09 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
None
Management information
Registered date
| 2025 | Year | 09 | Month | 25 | Day |
Last modified on
| 2025 | Year | 10 | Month | 14 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067693
