UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022250
Receipt number R000025637
Scientific Title Beneficial effects of tablet PC on cognitive function in the health elderly
Date of disclosure of the study information 2016/05/10
Last modified on 2016/11/08 12:38:17

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Basic information

Public title

Beneficial effects of tablet PC on cognitive function in the health elderly

Acronym

Beneficial effects of tablet PC

Scientific Title

Beneficial effects of tablet PC on cognitive function in the health elderly

Scientific Title:Acronym

Beneficial effects of tablet PC

Region

Japan


Condition

Condition

The healthy elderly

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to investigate the beneficial effects of processing speed training using Tablet PC on cognitive functions in the elderly

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Raven matrix test, digit span, story memory, Digit Symbol Coding (Cd) , Symbol Search(SS)(4 weeks after)

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Device,equipment Behavior,custom Other

Interventions/Control_1

Processing speed game intervention using tablet PC(15 minutes, 5 days per a week for 4 weeks)

Interventions/Control_2

Semantic knowledge game intervention using tablet PC(15 minutes, 5 days per a week for 4 weeks)

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

80 years-old >

Gender

Male and Female

Key inclusion criteria

We include participants who will report to be right-handed, native Japanese speakers, not concerned about their own memory functions, not using medications known to interfere with cognitive functions (including benzodiazepines, antidepressants or other central nervous agents), and having no diseases known to affect the central nervous system, including thyroid disease, multiple sclerosis, Parkinson's disease, stroke, severe hypertension or diabetes.

Key exclusion criteria

Person with medical history of the cerebral nerve disease
Person with medical history such as high blood pressure, the diabetes
Person who is participating in another cognitive-related training

Target sample size

72


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Rui Nouchi

Organization

Institute of Development, Aging and Cancer, Tohoku University

Division name

Smart Aging International Research Center

Zip code


Address

Seiryo-machi 4-1, Aoba-ku Sendai

TEL

022-717-8466

Email

rui.nouchi.a4@tohoku.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Rui Nouchi

Organization

Institute of Development, Aging and Cancer, Tohoku University

Division name

Smart Aging International Research Center

Zip code


Address

Seiryo-machi 4-1, Aoba-ku Sendai

TEL

022-717-8466

Homepage URL


Email

rui.nouchi.a4@tohoku.ac.jp


Sponsor or person

Institute

Tohoku Univeristy

Institute

Department

Personal name



Funding Source

Organization

Sharp Corporation

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


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



Other administrative information

Date of disclosure of the study information

2016 Year 05 Month 10 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

Completed

Date of protocol fixation

2016 Year 04 Month 01 Day

Date of IRB


Anticipated trial start date

2016 Year 04 Month 06 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

2016 Year 05 Month 09 Day

Last modified on

2016 Year 11 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000025637


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name