UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000015524
Receipt number R000018033
Scientific Title The effects of exercise on cognitive function in older adults with Mild Cognitive Impairment
Date of disclosure of the study information 2014/10/24
Last modified on 2014/10/24 16:49:51

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Basic information

Public title

The effects of exercise on cognitive function in older adults with Mild Cognitive Impairment

Acronym

The effects of exercise on cognitive function in older adults with Mild Cognitive Impairment

Scientific Title

The effects of exercise on cognitive function in older adults with Mild Cognitive Impairment

Scientific Title:Acronym

The effects of exercise on cognitive function in older adults with Mild Cognitive Impairment

Region

Japan


Condition

Condition

Mild Cognitive Impairment

Classification by specialty

Geriatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine whether physical exercise can help to prevent dementia caused by deposition of amyloid or not

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Examination of cerebrospinal fluid
(amiloid beta TNFalfa IL6 IL10)
Blood exam
(HOMA-R TNFalfa WBC RBC PLT)
Urinary test
Image Inspection
(MRI SPECT)
Mini Mental State Examination

Key secondary outcomes

*Clinical end-point
*FMD


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

YES

Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Behavior,custom

Interventions/Control_1

Exercise-intervention group:
aerobic exercise and resistance training
4 or more times a week for 6 months

Interventions/Control_2

Control Group: spend daily life

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

80 years-old >=

Gender

Male and Female

Key inclusion criteria

*Mild Cognitive Impairment(MCI) patients
*MMSE score above 24

Key exclusion criteria

*A previous history of cerebral infarction or paralysis. The patients with cranial nerve problem
*Having cardiovascular, respiratory or ophthalmologic disease
*Insulin self-injection
*Take Metformin or Biguanide

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroyuki Umegaki

Organization

Nagoya University

Division name

Department of Community Healthcare & Geriatrics, Graduate School of Medicine

Zip code


Address

65 Tsuruma-cho, Showa-ku, Nagoya

TEL

052-744-2364

Email

umegaki@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Hiroyuki Umegaki

Organization

Nagoya University

Division name

Department of Community Healthcare & Geriatrics, Graduate School of Medicine

Zip code


Address

65 Tsuruma-cho, Showa-ku, Nagoya

TEL

052-744-2364

Homepage URL


Email

umegaki@med.nagoya-u.ac.jp


Sponsor or person

Institute

Department of Community Healthcare & Geriatrics, Nagoya University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Ministry of Education, Culture, Sports, Science and Technology

Organization

Division

Category of Funding Organization

Nationality of Funding Organization

JAPAN


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

名古屋大学医学部附属病院(愛知県)
Nagoya University Hospital (Aichi prefecture)


Other administrative information

Date of disclosure of the study information

2014 Year 10 Month 24 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

No longer recruiting

Date of protocol fixation

2012 Year 04 Month 10 Day

Date of IRB


Anticipated trial start date

2012 Year 10 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 10 Month 24 Day

Last modified on

2014 Year 10 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018033


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name