UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000048877
Receipt number R000055664
Scientific Title Feasibility of Cognitive-Behavior Group Therapy for Depressive Disorders: Randomized Controlled Trial
Date of disclosure of the study information 2022/09/20
Last modified on 2024/03/08 12:05:02

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Basic information

Public title

Feasibility of Cognitive-Behavior Group Therapy for Depressive Disorders: Randomized Controlled Trial

Acronym

CoGrout Study

Scientific Title

Feasibility of Cognitive-Behavior Group Therapy for Depressive Disorders: Randomized Controlled Trial

Scientific Title:Acronym

CoGrout Study

Region

Japan


Condition

Condition

Depressive Disorder

Classification by specialty

Psychiatry

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to evaluate the feasibility of Cognitive-Behavioral Group Therapy for depressive disorders.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

Depressive symptom: PHQ-9(Patient Health Questionnaire

Key secondary outcomes

-Anxiety symptom: GAD-7(Generalized Anxiety Disorder)
-Self-Efficacy: GSES(General Self-Efficacy Scale)
-Personal Recovery: QPR-J(Japanese version of the Questionnaire about the Process of Recovery)
-Coping stress: CISS(Coping Inventory for Stressful Situation)
-QOL: WHO-QOL
-Disability: SDS(Sheehan Disability Scale)
-Others: Questionnaire on the use of CBT skills after participating in the group.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification

YES

Dynamic allocation

YES

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

Cognitive-Behavioral Group Therapy

Interventions/Control_2

Treatment as usual

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

70 years-old >=

Gender

Male and Female

Key inclusion criteria

1. Subjects with DSM-V Depression Disorder
2. Subjects with CGIS(Clinical Global Impression)score is 3(mildly ill ), 4(Moderately ill), or 5(Markedly ill)
3. Subjects between the ages of 18 and 70 at the time of screening
4. Subjects ca obtain written consent

Key exclusion criteria

1. No alcohol or substance use disorder in 24 months prior to the screening.
2. No history of concurrent manic, or psychotic episodes.
3. No other primary Axis I Disorders in 6 months prior to the screening.
4. No comorbid antisocial personality disorder.
5. No serious suicidal ideation at screening.
6. Unlikely to attend more than 4 visits during the 8-week trial phase.
7. No treatment of CBT or CBGT within the last year prior to the screening.
8. No organic brain lesions or major cognitive deficits.
9. No severe or unstable medical illness at screening.
10. Other relevant reasons decided by the CogGrout study principal investigator.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Toshiaki
Middle name
Last name Kikuchi

Organization

Keio University, School of Medicine

Division name

Department of Neuropsychiatry

Zip code

160-8582

Address

35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582

TEL

03-5363-3829

Email

kikuchi.psychiatry@gmail.com


Public contact

Name of contact person

1st name Miyuki
Middle name
Last name Tajima

Organization

Keio University School of Medicine

Division name

Department of Neuropsychiatry

Zip code

160-8582

Address

35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582

TEL

03-5363-3829

Homepage URL


Email

taji0808@gmail.com


Sponsor or person

Institute

Keio University, School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Grant in-Aid for Scientific Researchtific Research

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

1. Ichigaya Himorogi Clinic
2. Shinjuku Yoyogi Kokoro no Labo Clinic
3. Hamadayama Metal Clinic

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Research Ethics Committee of Keio University, School of Medicine

Address

35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582

Tel

03-3353-1211

Email

med-rinri-jimu@adst.keio.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

慶應義塾大学医学部/慶應義塾大学病院(東京都)


Other administrative information

Date of disclosure of the study information

2022 Year 09 Month 20 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

2022 Year 08 Month 29 Day

Date of IRB

2023 Year 03 Month 28 Day

Anticipated trial start date

2022 Year 10 Month 01 Day

Last follow-up date

2025 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

2022 Year 09 Month 07 Day

Last modified on

2024 Year 03 Month 08 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000055664


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name