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Name:
UMIN ID:

Recruitment status No longer recruiting
Unique ID issued by UMIN UMIN000024320
Receipt No. R000028011
Scientific Title Prospective Epidemiological Research on Functioning Outcomes related to Major Depressive Disorder in Japan
Date of disclosure of the study information 2016/10/06
Last modified on 2018/05/14

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Basic information
Public title Prospective Epidemiological Research on Functioning Outcomes related to Major Depressive Disorder in Japan
Acronym Prospective Epidemiological Research on Functioning Outcomes related to Major Depressive Disorder in Japan (PERFORM-J)
Scientific Title Prospective Epidemiological Research on Functioning Outcomes related to Major Depressive Disorder in Japan
Scientific Title:Acronym Prospective Epidemiological Research on Functioning Outcomes related to Major Depressive Disorder in Japan (PERFORM-J)
Region
Japan

Condition
Condition Major depressive disorder(MDD)
Classification by specialty
Psychosomatic Internal Medicine Psychiatry
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To assess the longitudinal pattern of cognitive function and depressive symptoms in MDD during episodes and following treatment over an observational period of 6 months.
Basic objectives2 Others
Basic objectives -Others Assessment of the longitudinal pattern of cognitive function and depressive symptoms in MDD during episodes and following treatment
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Changes from baseline in digit symbol substitution test (DSST) and Montgomery-Asberg depression scale (MADRS) after 2 and 6 months of treatment.
Key secondary outcomes The number of patients with cognitive dysfunction using multiple measures (DSST, Item 6 of MADRS and PDQ-D) and depressive symptoms (MADRS) in patients with MDD at baseline, after 2 and 6 months of treatment.
The association between cognitive dysfunction and psychosocial function in patients with MDD at baseline, after 2 and 6 months of treatment.
Comparison of quality of life and resource uses between MDD patients with different levels of cognitive dysfunction at baseline, after 2 and 6 months of treatment.

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
18 years-old <=
Age-upper limit
65 years-old >=
Gender Male and Female
Key inclusion criteria Patients who meet all of the following criteria are included in this study.
1.Outpatients
2.Patients aged between 18 and 65 years at the time of informed consent
3.Patients with a current or new diagnosis of major depressive episode according to Diagnostic and Statistical manual of Mental Disorders-IV (DSM-IV-TR); diagnosis will be confirmed through the MINI International Neuropsychiatric Interview (MINI questionnaire) (Major Depressive Episode module).
4.Patients initiating a new antidepressant monotherapy (tricyclic or tetracyclic antidepressant, SSRI, SNRI, NaSSA) at the baseline visit (whether as first line or switch of antidepressant therapy) as decided by the investigator.
5.Patients who, in the opinion of the investigator, are capable of understanding the content of the clinical research and complying with the research protocol requirements.
6.Patients who can sign and date an informed consent form prior to the conduction of the clinical research procedures.
7.Patients who are capable of reading and understanding questionnaire
Key exclusion criteria Patients who fall into any of the following criteria are excluded from participating in this study.
1.Patients who have a concurrent diagnosis or past history of any of the following conditions:
Schizophrenia or other psychotic disorders
.Bipolar disorders
.Dementia or any other neurodegenerative disease
.Substance dependence, including alcohol and other drugs, excluding mild and moderate nicotine dependence. Severe nicotine dependence will be excluded.
.Any psychiatric disorder due to a general medical condition or substances
2.Patients prescribed with more than 1 antidepressant on the day of the baseline visit (combination of 2 or more antidepressants)
3.Patients prescribed antipsychotic on the day of the baseline visit (augmentation of the antidepressant prescription with an antipsychotic)
4.Patients prescribed mood stabilizers on the day of the baseline visit (augmentation of the antidepressant prescription with a mood stabilizer)
5.Patients having current treatment with electroconvulsive therapy (ECT) or repeated transcranial magnetic stimulation (rTMS)
6.Pregnant women, women breast feeding at the start of the research
7.Patients presenting acute suicidality in the investigator's opinion
8.Patients currently enrolled in an interventional clinical research such as clinical trial
9.Member of the research personnel or their immediate families, or subordinates (or immediate family member of a subordinate) to any of the research personnel.
10.Patient who has previously been enrolled in this research
11.Patients who, in the opinion of the investigator, unlikely to comply with the protocol
Target sample size 500

Research contact person
Name of lead principal investigator
1st name
Middle name
Last name Tomiki Sumiyoshi
Organization National Center of Neurology and Psychiatry
Division name Department of Clinical Epidemiology
Zip code
Address 4-1-1 Ogawahigashimachi, Kodaira,Tokyo 187-8551, Japan
TEL 042-341-2711
Email sumiyot@ncnp.go.jp

Public contact
Name of contact person
1st name
Middle name
Last name Kotaro Senuki
Organization Sogo Rinsho Medefi Company Limited.
Division name Business promotion department
Zip code
Address 9F KDX Shinjuku building 3-2-7,Nishishinjuku,Shinjuku-ku,Tokyo
TEL 03-6901-6079
Homepage URL
Email PERFORM-J@sogo-medefi.jp

Sponsor
Institute Takeda Pharmaceutical Company Limited.
Institute
Department

Funding Source
Organization Takeda Pharmaceutical Company Limited.
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 10 Month 06 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
2016 Year 08 Month 25 Day
Date of IRB
Anticipated trial start date
2016 Year 10 Month 06 Day
Last follow-up date
2018 Year 01 Month 10 Day
Date of closure to data entry
2018 Year 04 Month 02 Day
Date trial data considered complete
2018 Year 05 Month 10 Day
Date analysis concluded

Other
Other related information The prospective clinical study for Functioning Outcomes related to Major Depressive Disorder.

Management information
Registered date
2016 Year 10 Month 06 Day
Last modified on
2018 Year 05 Month 14 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028011

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


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