UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056170
Receipt number R000064181
Scientific Title Sources, topics and acquisition routes and timing of health information acquired by women and their partners in the perinatal and postpartum periods: a scoping review
Date of disclosure of the study information 2024/11/16
Last modified on 2026/05/19 11:24:05

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Basic information

Public title

Sources, topics and acquisition routes and timing of health information acquired by women and their partners in the perinatal and postpartum periods: a scoping review

Acronym

Sources and topics of health information acquired by women and their partners in the perinatal and postpartum periods: a scoping review

Scientific Title

Sources, topics and acquisition routes and timing of health information acquired by women and their partners in the perinatal and postpartum periods: a scoping review

Scientific Title:Acronym

Sources and topics of health information acquired by women and their partners in the perinatal and postpartum periods: a scoping review

Region

Japan


Condition

Condition

Pregnancy, labor, delivery, and postpartum

Classification by specialty

Obstetrics and Gynecology Nursing Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To map and synthesise evidence on the acquisition of health information by women and their partners during the perinatal and postpartum periods and clarify the relationships between the sources and topics of health information and the acquisition of health information.

Basic objectives2

Others

Basic objectives -Others

To generate thorough knowledge of relationships and patterns from the answers to our research questions as follows: (1) What are the relationships between the sources and topics of health information that women and their partners acquire during the perinatal and postpartum periods? (2) What are the patterns of acquisition of health information by women and their partners? (3) What are the patterns of acquisition routes and timing of health information by women and their partners?

Trial characteristics_1

Exploratory

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

The sources of health information and the topics identified by women and their partners in the perinatal and postpartum periods.

Key secondary outcomes

For the women and their partners, what are their sources of health information, what are the topics they obtain information on in the perinatal and postpartum periods.


Base

Study type

Others,meta-analysis etc


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

The Population, Concept, and Context (PCC) framework by the Joanna Briggs Institute (JBI) methodology will be used for establishing the eligibility criteria. The inclusion criteria will be as follows:
P: Women and their partners in the perinatal and postpartum periods.
C: Sources of health information related to the perinatal and postpartum periods and topics that the population acquired during these periods, focusing on their physical and mental health, routes and timing of information acquisition. As the routes and timing of acquisition of health information have not yet been investigated in relation to the sources of evidence, these items will be included in this scoping review.
C: Open (ie, not limited by country or culture). This scoping review will consider a broad range of sources of evidence that address our research questions. This includes primary research articles (eg, observational studies including descriptive cross-sectional studies, prospective longitudinal studies, retrospective longitudinal studies and qualitative studies/reviews) and other relevant grey literature (eg, reports by the government, institutions, non-profit organisations, professional associations and patient groups). We will include sources of evidence that were investigated after 2020.If reviews are included, the articles cited in these reviews will be excluded.

Key exclusion criteria

Health information regarding breastfeeding, foetus and baby; sources of evidence that are written in languages other than English or Japanese; and conference abstracts and protocols.

Target sample size



Research contact person

Name of lead principal investigator

1st name Yuriko
Middle name
Last name Tadokoro

Organization

Tokyo Healthcare University

Division name

Chiba Faculty of Nursing

Zip code

273-8710

Address

1-1042-2 Kaijincho nishi, Funabashi-shi, Chiba 273-8710, Japan

TEL

047-495-7751

Email

y-tadokoro@thcu.ac.jp


Public contact

Name of contact person

1st name Yuriko
Middle name
Last name Tadokoro

Organization

Tokyo Healthcare University

Division name

Chiba Faculty of Nursing

Zip code

273-8710

Address

1-1042-2 Kaijincho nishi, Funabashi-shi, Chiba 273-8710, Japan

TEL

047-495-7751

Homepage URL


Email

y-tadokoro@thcu.ac.jp


Sponsor or person

Institute

Tokyo Healthcare University

Institute

Department

Personal name



Funding Source

Organization

JSPS KAKENHI Grant Number 24K20356.

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

N/A

Address

N/A

Tel

N/A

Email

N/A


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

2024 Year 11 Month 16 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

2024 Year 07 Month 31 Day

Date of IRB

2024 Year 07 Month 31 Day

Anticipated trial start date

2024 Year 08 Month 01 Day

Last follow-up date

2026 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This is a scoping review, therefore, no patient registration is planned. Terefore, no patients will be enrolled. Additionally, ethical approval for the study is not required. Since all fields must be completed to register the study on UMIN, appropriate entries have been made in each section.


Management information

Registered date

2024 Year 11 Month 16 Day

Last modified on

2026 Year 05 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064181