UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000049467
Receipt number R000056325
Scientific Title Verification of the effect of breast massage care on breast engorgement
Date of disclosure of the study information 2023/01/01
Last modified on 2022/11/09 14:19:00

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Basic information

Public title

Verification of the effect of breast massage care on breast engorgement

Acronym

Verification of the effect of breast massage care on breast engorgement

Scientific Title

Verification of the effect of breast massage care on breast engorgement

Scientific Title:Acronym

Verification of the effect of breast massage care on breast engorgement

Region

Japan


Condition

Condition

Women who have a normal pregnancy and delivery process for both mother and child and wish to breastfeed.

Classification by specialty

Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The course of breast engorgement symptoms that appeared in the early postpartum period will be clarified in relation to changes in udder findings and intramammary blood flow.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Axillary, lateral thoracic, and medial thoracic arteriovenous blood flow
(around 36 weeks gestation, 1st, 3rd, and 5th days postpartum)
Evaluate twice on the third postpartum day only: before breast massage and after massage and breastfeeding.

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

18 years-old <=

Age-upper limit

50 years-old >

Gender

Female

Key inclusion criteria

Planned vaginal delivery of a single fetus

Key exclusion criteria

Women with psychiatric complications, abnormal glucose metabolism, cardiac disease, history of hypertension, and history of breast disease and its surgery

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Yumiko
Middle name
Last name Tateoka

Organization

Shiga University of Medical Science

Division name

Course of Nursing

Zip code

5202144

Address

Seta Tsukinawa-cho, Otsu City, Shiga

TEL

0775482111

Email

ytateoka@belle.shiga-med.ac.jp


Public contact

Name of contact person

1st name Yumiko
Middle name
Last name Tateoka

Organization

Shiga University of Medical Science

Division name

Course of Nursing

Zip code

5202144

Address

Seta Tsukinawa-cho, Otsu City, Shiga

TEL

0775482111

Homepage URL


Email

ytateoka@belle.shiga-med.ac.jp


Sponsor or person

Institute

Shiga University of Medical Science

Institute

Department

Personal name



Funding Source

Organization

Shiga University of Medical Science

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Shiga University of Medical Science

Address

Seta Tsukinawa-cho, Otsu City, Shiga

Tel

0775482111

Email

ytateoka@belle.shiga-med.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

2023 Year 01 Month 01 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

Preinitiation

Date of protocol fixation

2022 Year 05 Month 25 Day

Date of IRB


Anticipated trial start date

2023 Year 01 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

None


Management information

Registered date

2022 Year 11 Month 09 Day

Last modified on

2022 Year 11 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000056325


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name