UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000044704
Receipt number R000051045
Scientific Title The effect of memory retrieval on decision-making in healthy subjects
Date of disclosure of the study information 2021/06/29
Last modified on 2023/07/04 09:07:58

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Basic information

Public title

The effect of memory retrieval on decision-making in healthy subjects

Acronym

The effect of memory retrieval on decision-making in healthy subjects

Scientific Title

The effect of memory retrieval on decision-making in healthy subjects

Scientific Title:Acronym

The effect of memory retrieval on decision-making in healthy subjects

Region

Japan


Condition

Condition

Depression

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the effect of positive autobiographical memory retrieval on decision-making in healthy subjects

Basic objectives2

Others

Basic objectives -Others

To investigate whether the above effect depends on personal characteristics of the subjects

Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

1) Decision-making task performance
2) Behavioral parameters estimated using behavioral modeling (such as risk preference)

Key secondary outcomes

1) The change of mood caused by memory retrieval
2) Whether the effect of memory retrieval on decision making depends on mood change
3) Whether the effect of memory retrieval on decision making depends on subjects' personal characteristics
4) Relationships among other personal characteristics


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -investigator(s) and assessor(s) are blinded

Control

Placebo

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

YES

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

Positive autobiographical memory retrieval. Using 20 positive memories selected based on an autobiographical memory questionnaire administered on a separate day beforehand. The cues of the memories are presented to the subjects and they are asked to recall the corresponding memory vividly, after which they assess the valence and emotional intensity of the memory, as well as how they feel after recalling that memory.

Interventions/Control_2

Control intervention: neutral autobiographical memory retrieval. Using 20 neutral memories selected from the above memory questionnaire.

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

20 years-old <=

Age-upper limit

29 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Age is 20 to 29 at the time of obtaining consent.
2) Regardless of gender.
3) A person who, after receiving a sufficient explanation before participating in this research, has a sufficient understanding and provided informed consent.

Key exclusion criteria

1) Those who are currently suffering from a memory impairment or are currently undergoing medical examination (including those who are scheduled to undergo medical examination) in order to confirm if they have memory impairment, by self-declaration.
2) Those who are currently suffering from a mental illness or are currently undergoing medical examination (including those who are scheduled to undergo medical examination), by self-declaration.
3) Those who cannot recall at least 20 positive and 20 negative autobiographical memories in response to the autobiographical memory questionnaire.
4) Those who are judged to be unsuitable as research subjects by the researcher in charge of the experimental sessions (for example, subjects who cannot conduct the decision-making task smoothly due to physical conditions).

Target sample size

34


Research contact person

Name of lead principal investigator

1st name Shin
Middle name
Last name Nakagawa

Organization

Yamaguchi University Graduate School of Medicine

Division name

Division of Neuropsychiatry, Department of Neuroscience

Zip code

7558505

Address

Minamikogushi 1-1-1, Ube, Yamaguchi, Japan

TEL

0836222255

Email

brain@yamaguchi-u.ac.jp


Public contact

Name of contact person

1st name Chong
Middle name
Last name Chen

Organization

Yamaguchi University Graduate School of Medicine

Division name

Division of Neuropsychiatry, Department of Neuroscience

Zip code

7558505

Address

Minamikogushi 1-1-1, Ube, Yamaguchi, Japan

TEL

7558505

Homepage URL


Email

brain@yamaguchi-u.ac.jp


Sponsor or person

Institute

Division of Neuropsychiatry, Department of Neuroscience, Yamaguchi University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Institutional Review Board Committee in Yamaguchi University Hospital

Address

Minamikogushi 1-1-1, Ube, Yamaguchi, Japan

Tel

0836222428

Email

clin_res@yamaguchi-u.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 06 Month 29 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

Main results already published

Date of protocol fixation

2021 Year 06 Month 28 Day

Date of IRB

2021 Year 06 Month 29 Day

Anticipated trial start date

2021 Year 07 Month 05 Day

Last follow-up date

2023 Year 03 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 06 Month 29 Day

Last modified on

2023 Year 07 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051045


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name