UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000001970
Receipt number R000002396
Scientific Title The investigation of prospective memory process with the Cambridge Prospective Memory Test (CAMPROMPT)-Japanese
Date of disclosure of the study information 2009/06/10
Last modified on 2016/07/28 19:08:40

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Basic information

Public title

The investigation of prospective memory process with the Cambridge Prospective Memory Test (CAMPROMPT)-Japanese

Acronym

The investigation of prospective memory process with CAMPROMPT-Japanese

Scientific Title

The investigation of prospective memory process with the Cambridge Prospective Memory Test (CAMPROMPT)-Japanese

Scientific Title:Acronym

The investigation of prospective memory process with CAMPROMPT-Japanese

Region

Japan


Condition

Condition

Cerebrovascular disease
Traumatic brain injury
Mild cognitive impairment
Alzheimer's disease
Frontotemporal dementia
Dementia with Lewy bodies

Classification by specialty

Neurology Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate prospective memory impairment with the Cambridge Prospective Memory Test (CAMPROMPT)-Japanese

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The Cambridge Prospective Memory Test (CAMPROMPT)-Japanese

Key secondary outcomes

Wechsler Adult Intelligence Scale 3/Revised
Mini-Mental State Examination
Kana-hiroi test
Supplementary Tests for Standard Language Test of Aphasia,"Explanation of Katoons"
The Rivermead Behavioural Memory Test-Japanese with check lists
Behavioural Assessment of the Dysexecutive Syndrome-Japanese with DEX questionaires


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


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

16 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients with memory impairment or/and frontal function impairment after acquired cerebral damage

Key exclusion criteria

1.Patients with aphasia
2.Patients with depression or some psychiatric disease
3. Patients with congenital mental retardation
4. Patients with severe dementia

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Jun Tanemura

Organization

Kawasaki University of Medical Welfare

Division name

Faculty of Health Science and Technology, Department of Sensory Science

Zip code


Address

288 Matushima Kurashiki-city Okayama-prefecture

TEL

086-427-1111(54631)

Email



Public contact

Name of contact person

1st name
Middle name
Last name Jun Tanemura

Organization

Kawasaki University of Medical Welfare

Division name

Faculty of Health Science and Technology, Department of Sensory Science

Zip code


Address

288 Matushima Kurashiki-city Okayama-prefecture

TEL

086-427-1111(54631)

Homepage URL


Email

tanemura@mw.kawasaki-m.ac.jp


Sponsor or person

Institute

Kawasaki University of Medical Welfare

Institute

Department

Personal name



Funding Source

Organization

Kawasaki University of Medical Welfare

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

Kawasaki Medical School Hospital
Kawasaki Hpopital, Kawasaki Medical School

Name of secondary funder(s)

None


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

2009 Year 06 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

Date of protocol fixation

2009 Year 03 Month 01 Day

Date of IRB


Anticipated trial start date

2009 Year 03 Month 01 Day

Last follow-up date

2011 Year 03 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

To investigate prospective memory impaiment with CAMPROMPT.


Management information

Registered date

2009 Year 05 Month 14 Day

Last modified on

2016 Year 07 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000002396


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name