UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000015878
Receipt number R000018467
Scientific Title Effect of postpartum pelvic floor muscle training with ultrasound biofeedback on recovery of pelvic floor muscle function: a randomized controlled trial
Date of disclosure of the study information 2014/12/08
Last modified on 2016/12/09 17:46:50

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Basic information

Public title

Effect of postpartum pelvic floor muscle training with ultrasound biofeedback on recovery of pelvic floor muscle function: a randomized controlled trial

Acronym

Effect of postpartum pelvic floor muscle training with ultrasound biofeedback

Scientific Title

Effect of postpartum pelvic floor muscle training with ultrasound biofeedback on recovery of pelvic floor muscle function: a randomized controlled trial

Scientific Title:Acronym

Effect of postpartum pelvic floor muscle training with ultrasound biofeedback

Region

Japan


Condition

Condition

Pelvic floor muscle dysfunction
Urinary stress incontinence
Fecal incontinence

Classification by specialty

Obstetrics and Gynecology Urology Nursing
Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The study aims to evaluate the effectiveness of postpartum pelvic floor muscle training with ultrasound biofeedback for the recovery of pelvic floor muscle function.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Evaluation of pelvic floor muscle function using ultrasounds

Key secondary outcomes

1) Ultrasound evaluation of the success rate in the pelvic floor muscle contraction at each lesson

2) Questionnaires
Pelvic floor distress inventory-20(PFDI-20)
Fecal incontinence severity index(FISI)
International consultation on incontinence questionnaire-short form(ICIQ-SF)
Fatigue feelings(Jikakusho shirabe)
Fecal incontinence quality of life scale(FIQL)
Wexner score
Incontinence quality of life(I-QOL)
Pelvic floor muscle exercise self-efficacy scale


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

No treatment

Stratification

YES

Dynamic allocation


Institution consideration


Blocking

YES

Concealment

Central registration


Intervention

No. of arms

3

Purpose of intervention

Treatment

Type of intervention

Behavior,custom Maneuver

Interventions/Control_1

Postpartum pelvic floor muscle training with ultrasound biofeedback

Interventions/Control_2

Postpartum pelvic floor muscle training without ultrasound biofeedback

Interventions/Control_3

Usual care

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


Not applicable

Gender

Female

Key inclusion criteria

Primiparous postpartum women

Key exclusion criteria

1) with a history of cesarean section, multiple birth or breech delivery
2) with an experience of incontinence before pregnancy
3) with neuropathic urinary and fecal incontinence
4) with restricted physical activity
5) less than 20 years old

Target sample size

180


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Megumi Haruna

Organization

The University of Tokyo

Division name

Division of Health Sciences & Nursing, Graduate School of Medicine

Zip code


Address

7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan

TEL

03-5841-3396

Email

mharuna-tky@umin.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yurie Asai

Organization

The University of Tokyo

Division name

Division of Health Sciences & Nursing, Graduate School of Medicine

Zip code


Address

7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan

TEL

03-5841-3396

Homepage URL


Email

Yurieasai-tky@umin.ac.jp


Sponsor or person

Institute

The University of Tokyo

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science

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


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

2014 Year 12 Month 08 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

Completed

Date of protocol fixation

2014 Year 12 Month 05 Day

Date of IRB


Anticipated trial start date

2014 Year 12 Month 08 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 12 Month 08 Day

Last modified on

2016 Year 12 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018467


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name