UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000060851
Receipt number R000069632
Scientific Title Exploratory study of the efficacy of food ingredients on walking speed
Date of disclosure of the study information 2026/03/09
Last modified on 2026/03/06 16:43:00

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Basic information

Public title

Exploratory study of the efficacy of food ingredients on walking speed in healthy men and women (SWE-2026-01-HBLOCO)

Acronym

Exploratory study of the efficacy of food ingredients on walking speed

Scientific Title

Exploratory study of the efficacy of food ingredients on walking speed

Scientific Title:Acronym

Exploratory study of the efficacy of food ingredients on walking speed

Region

Japan


Condition

Condition

Not applicable

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the effect of food ingredients on walking speed

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Amount of change of normal walking speed over 6 m

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Intake of the test foods A (40 weeks)
Interviews regarding trial

Interventions/Control_2

Intake of the test foods B (40 weeks)
Interviews regarding trial

Interventions/Control_3

Intake of the Placebo foods (40 weeks)
Interviews regarding trial

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

40 years-old <=

Age-upper limit

74 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Healthy men and women aged 40 to 74 years from the time of obtaining consent to the scheduled completion date of the final inspection.
2) Person with or without knee pain.
3) Person who can understand the purpose and content of this study and agree in writing to participate in this study.

Key exclusion criteria

1) Presence of disease in locomotor organs affecting the efficacy assessment of this study.
2) Person whose keep irregular hours such as shift work.
3) Use of product affecting the data of this study, such as food for specified health use, food with function claims, and medicine.
4) Presence of previous and present serious disease such as cardiac affection, liver disorder, kidney disorder, cardiovascular disorder, lung disorder, diabetes mellitus.
5) Investigator's judgment for other reason.

Target sample size

425


Research contact person

Name of lead principal investigator

1st name Hisnori
Middle name
Last name Tokuda

Organization

Suntory Wellness Limited

Division name

Institute for Science of Life

Zip code

619-0284

Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto. 619-0284, Japan.

TEL

050-1804-0218

Email

Hisnori_Tokuda@suntory.co.jp


Public contact

Name of contact person

1st name Kosuke
Middle name
Last name Suzuki

Organization

Suntory Wellness Limited

Division name

Institute for Science of Life

Zip code

619-0284

Address

8-1-1 Seikadai, Seika-cho, Soraku-gun, Kyoto. 619-0284, Japan.

TEL

050-1804-0235

Homepage URL


Email

Kosuke_Suzuki@suntory.co.jp


Sponsor or person

Institute

Suntory Wellness Limited

Institute

Department

Personal name



Funding Source

Organization

None

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

Medical Station Clinic Research Ethics Committee

Address

3-12-8, Takaban, Meguroku, Tokyo

Tel

03-6452-2712

Email

epmd_fd-erb@eps.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 03 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


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 02 Month 26 Day

Date of IRB


Anticipated trial start date

2026 Year 03 Month 10 Day

Last follow-up date

2027 Year 04 Month 02 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2026 Year 03 Month 06 Day

Last modified on

2026 Year 03 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000069632