UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000041634
Receipt number R000047523
Scientific Title Effect of frequency of aerobic exercise training on arterial stiffness after glucose ingestion
Date of disclosure of the study information 2020/10/01
Last modified on 2021/10/21 10:38:46

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Basic information

Public title

Effect of frequency of aerobic exercise training on arterial stiffness after glucose ingestion

Acronym

Effect of frequency of aerobic exercise training on arterial stiffness after glucose ingestion

Scientific Title

Effect of frequency of aerobic exercise training on arterial stiffness after glucose ingestion

Scientific Title:Acronym

Effect of frequency of aerobic exercise training on arterial stiffness after glucose ingestion

Region

Japan


Condition

Condition

Arteriosclerosis

Classification by specialty

Cardiology Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The present study aimed to determine the effects of frequency of aerobic exercise training on arterial stiffness after glucose ingestion in the middle-aged and elderly.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Subjects will receive the following measurements before, 4 and 8 weeks after training. Measure pulse wave velocity (PWV), blood pressure, heart rate, and blood glucose level before, 30, 60, and 90 min after glucose ingesting. From the above, changes in PWV, blood pressure, heart rate, and blood glucose level are evaluated.

Key secondary outcomes

Subjects will receive the following measurements before, 4 and 8 weeks after training. Height, weight and body fat percentage are measured before glucose ingestion. 90 min after glucose ingestion, measure the peak oxygen uptake. From the above, changes in Height, weight and body fat percentage, and peak oxygen uptake are evaluated.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Behavior,custom

Interventions/Control_1

Aerobic exercise training (walking, jogging)
8 weeks
Moderate intensity (50-60% of the age-predicted maximum heart rate)
30 minutes/time
2 days a week

Interventions/Control_2

Aerobic exercise training (walking, jogging)
8 weeks
Moderate intensity (50-60% of the age-predicted maximum heart rate)
30 minutes/time
4 days a week

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

45 years-old <=

Age-upper limit

80 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Schedule can be adjusted
2) Body mass index (BMI) is less than 18.5 to 25 kg / m2
3) You can follow the precautions when participating in the experiment
4) No smoking habits
5) Subjects who agree to participate in this study with a written informed consent after receiving sufficient explanation relating to this study.

Key exclusion criteria

1) If you have a chronic disease
2) When the subject has severe physical symptoms and it is difficult to cooperate with the research
3) In addition, if the person in charge of the survey judges it inappropriate to participate

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Ryota
Middle name
Last name Kobayashi

Organization

Teikyo University of Science

Division name

Center for Fundamental Education

Zip code

120-0045

Address

2-2-1 Senju, Sakuragi, Adachi-ku, Tokyo, Japan

TEL

03-6910-1010

Email

rkobayashi@ntu.ac.jp


Public contact

Name of contact person

1st name Ryota
Middle name
Last name Kobayashi

Organization

Teikyo University of Science

Division name

Center for Fundamental Education

Zip code

Center for Fundamental Education

Address

2-2-1 Senju, Sakuragi, Adachi-ku, Tokyo, Japan

TEL

03-6910-1010

Homepage URL


Email

rkobayashi@ntu.ac.jp


Sponsor or person

Institute

Center for Fundamental Education, Teikyo University of Science

Institute

Department

Personal name



Funding Source

Organization

Ministry of Education, Culture, Sports, Science and Technology

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

Teikyo University of Science

Address

2-2-1 Senju, Sakuragi, Adachi-ku, Tokyo, Japan

Tel

03-6910-1010

Email

kenkyushien@ntu.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

帝京科学大学(東京都)


Other administrative information

Date of disclosure of the study information

2020 Year 10 Month 01 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

20

Results

Pre-of exercises, the baPWV increased at 30 (p < 0.05), 60 (p < 0.01) and 90 min (p < 0.01) after glucose ingestion in the T2 group. The baPWV increased at 30 (p < 0.05), 60 (p < 0.01) and 90 min (p < 0.01) after glucose ingestion in the T4 group. After eight weeks of exercise, the baPWV increased at 30 (p < 0.05) and 60 min (p < 0.05) after glucose ingestion and remained unchanged at 90 min in the T2 group. The baPWV was unchanged at 30, 60, and 90 min after glucose ingestion in the T4 group.

Results date posted

2021 Year 10 Month 21 Day

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

2020 Year 09 Month 30 Day

Date of IRB

2020 Year 11 Month 11 Day

Anticipated trial start date

2020 Year 12 Month 01 Day

Last follow-up date

2021 Year 03 Month 31 Day

Date of closure to data entry

2021 Year 03 Month 31 Day

Date trial data considered complete

2021 Year 03 Month 31 Day

Date analysis concluded

2021 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2020 Year 09 Month 01 Day

Last modified on

2021 Year 10 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000047523


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name