UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000044308
Receipt number R000050416
Scientific Title Impact of resilience characteristics and coping on postpartum depression among fathers and mothers: A longitudinal observational study.
Date of disclosure of the study information 2021/05/24
Last modified on 2021/05/24 20:38:03

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Basic information

Public title

Impact of resilience characteristics and coping on postpartum depression among fathers and mothers: A longitudinal observational study.

Acronym

Impact of resilience characteristics and coping on postpartum depression.

Scientific Title

Impact of resilience characteristics and coping on postpartum depression among fathers and mothers: A longitudinal observational study.

Scientific Title:Acronym

Impact of resilience characteristics and coping on postpartum depression.

Region

Japan


Condition

Condition

postpartum depression

Classification by specialty

Obstetrics and Gynecology Psychiatry Nursing
Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clear how resilience characteristics and coping at 1 month postpartum affect subsequent depressive symptoms among parents.

Basic objectives2

Others

Basic objectives -Others

Exploring related factors

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Postpartum depression (Edinburgh Postnatal Depression Scale; EPDS)

Key secondary outcomes



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

20 years-old <=

Age-upper limit

50 years-old >=

Gender

Male and Female

Key inclusion criteria

(1) Pregnant women and the heterosexual partners
(2) 20 y/o or older
(3) Able to read and write Japanese

Key exclusion criteria

In case which participation to this study until 12 months postpartum is not expected, such as because of severe prognosis on fetus.

Target sample size

140


Research contact person

Name of lead principal investigator

1st name Yoko
Middle name
Last name Takeishi

Organization

Tohoku University Graduate School of Medicine

Division name

Department of Women's Health Nursing &midwifery

Zip code

9808575

Address

2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi

TEL

0227177933

Email

yoko.takeishi@med.tohoku.ac.jp


Public contact

Name of contact person

1st name Yoko
Middle name
Last name Takeishi

Organization

Tohoku University Graduate School of Medicine

Division name

Department of Women's Health Nursing &midwifery

Zip code

9808575

Address

2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi

TEL

0227177933

Homepage URL


Email

yoko.takeishi@med.tohoku.ac.jp


Sponsor or person

Institute

Tohoku University

Institute

Department

Personal name



Funding Source

Organization

Ministry of Education, Culture, Sports, Science and Technology

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tohoku University Graduate School of Medicine

Address

2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi

Tel

0227177933

Email

yoko.takeishi@med.tohoku.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 05 Month 24 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

Enrolling by invitation

Date of protocol fixation

2021 Year 03 Month 10 Day

Date of IRB

2021 Year 05 Month 10 Day

Anticipated trial start date

2021 Year 05 Month 24 Day

Last follow-up date

2023 Year 05 Month 24 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

To investigate depressive symptoms and related factors for fathers and mothers 1, 3, 6 and 12 months after childbirth.


Management information

Registered date

2021 Year 05 Month 24 Day

Last modified on

2021 Year 05 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000050416


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name