UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000031369
Receipt number R000035804
Scientific Title The change of physical strength during pregnancy and postpartum
Date of disclosure of the study information 2018/02/24
Last modified on 2018/02/19 15:20:13

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Basic information

Public title

The change of physical strength during pregnancy and postpartum

Acronym

The change of physical strength during pregnancy and postpartum

Scientific Title

The change of physical strength during pregnancy and postpartum

Scientific Title:Acronym

The change of physical strength during pregnancy and postpartum

Region

Japan


Condition

Condition

healthy pregnant and postpartum women (within a year after childbirth)

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify changes in physical strength associated with pregnancy and its recovery process

Basic objectives2

Others

Basic objectives -Others

Assessment of physical strength

Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Muscle strength of pregnant and postpartum women (within a year after childbirth)

Key secondary outcomes

balance ability, physical activity


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


Not applicable

Gender

Female

Key inclusion criteria

pregnant or postpartum women (within a year after childbirth)

Key exclusion criteria

The patient who has central nervous system or musculoskeletal disease

Target sample size

150


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Kajiwara Yu

Organization

Kio University

Division name

Faculty of Health Science

Zip code


Address

4-2-2 Umaminaka Koryocho Kitakatsuragigun Nara

TEL

0745541601

Email

y.kajiwara@kio.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Kajiwara Yu

Organization

Kio University

Division name

Faculty of Health Science

Zip code


Address

4-2-2 Umaminaka Koryocho Kitakatsuragigun Nara

TEL

0745541601

Homepage URL


Email

y.kajiwara@kio.ac.jp


Sponsor or person

Institute

Kio University

Institute

Department

Personal name



Funding Source

Organization

Kio University

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


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

2018 Year 02 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

Preinitiation

Date of protocol fixation

2018 Year 02 Month 19 Day

Date of IRB


Anticipated trial start date

2018 Year 02 Month 24 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

study design: cross-sectional study
subject: participants who come to health promotion events and agree with attention to this study
assessment: grip strength, grip strength of foot, functional reach test, IPAQ Japanese version, locomotive syndrome check test, demographic data,


Management information

Registered date

2018 Year 02 Month 19 Day

Last modified on

2018 Year 02 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000035804


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name