UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000044966
Receipt number R000051373
Scientific Title The effect of soy peptide intake on sarcopenia and cognitive decline: A randomized controlled trial
Date of disclosure of the study information 2021/08/05
Last modified on 2021/07/27 12:05:27

* 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

The effect of soy peptide intake on sarcopenia and cognitive decline: A randomized controlled trial

Acronym

The effect of soy peptide intake on physical and cognitive functions

Scientific Title

The effect of soy peptide intake on sarcopenia and cognitive decline: A randomized controlled trial

Scientific Title:Acronym

The effect of soy peptide intake on physical and cognitive functions

Region

Japan


Condition

Condition

Healthy subject

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy of soy peptide on physical and cognitive functions

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Number of correct answers on nueropsychological tests
skeletal muscle index
grip strength
Timed & Up Go Test

Key secondary outcomes

Blood parameter


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification

YES

Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

Intervention group: soy peptide containing drink 190g, 3 months

Interventions/Control_2

Control group: non-intake of soy peptide containing drink

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

60 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. Elderly adults who have participated in
cohort studies
2. Independent person in their activities
of daily living and do not utilize
Japan's long-term care service

Key exclusion criteria

1. Patient with dementia
2. Patient with severe cardiac, pulmonary,
neurological or musculoskeletal disorders
3. Patient with food, and/or specifically
soy allergy

Target sample size

90


Research contact person

Name of lead principal investigator

1st name Itsushi
Middle name
Last name Takai

Organization

Osaka University of Economics

Division name

Department of Human Sciences

Zip code

533-8533

Address

2-2-8, Osumi, Higashiyodogawa-ku, Osaka, 533-8533 Japan

TEL

06-6328-2431

Email

takai@osaka-ue.ac.jp


Public contact

Name of contact person

1st name Itsushi
Middle name
Last name Takai

Organization

Osaka University of Economics

Division name

Department of Human Sciences

Zip code

533-8533

Address

2-2-8, Osumi, Higashiyodogawa-ku, Osaka, 533-8533 Japan

TEL

06-6328-2431

Homepage URL


Email

takai@osaka-ue.ac.jp


Sponsor or person

Institute

Osaka University of Economics

Institute

Department

Personal name



Funding Source

Organization

Fuji Oil Co. Ltd.,

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Fuji Oil Co. Ltd.,

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Human Ethics Committee, Osaka University of Economics

Address

2-2-8, Osumi, Higashiyodogawa-ku, Osaka, 533-8533 Japan

Tel

06-6328-2431

Email

kenkyuu@osaka-ue.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

2021 Year 08 Month 05 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

97

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

Completed

Date of protocol fixation

2018 Year 07 Month 03 Day

Date of IRB

2018 Year 08 Month 22 Day

Anticipated trial start date

2018 Year 09 Month 01 Day

Last follow-up date

2021 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2021 Year 07 Month 27 Day

Last modified on

2021 Year 07 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051373


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name