UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000058791 |
|---|---|
| Receipt number | R000067218 |
| Scientific Title | Effectiveness of social media-based interventions to improve urinary incontinence among women: a non-blind randomized control trial |
| Date of disclosure of the study information | 2025/09/16 |
| Last modified on | 2025/08/13 14:44:56 |
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Basic information
Public title
Effectiveness of social media-based interventions to improve urinary incontinence among women: a non-blind randomized control trial
Acronym
Effectiveness of social media-based interventions to improve urinary incontinence among women: a non-blind randomized control trial
Scientific Title
Effectiveness of social media-based interventions to improve urinary incontinence among women: a non-blind randomized control trial
Scientific Title:Acronym
Effectiveness of social media-based interventions to improve urinary incontinence among women: a non-blind randomized control trial
Region
| Japan |
Condition
Condition
Urinary incontinence
Classification by specialty
| Nursing |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The objective of this study is to assess the efficacy of an 8-week social media-based intervention for women with urinary incontinence.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Cure of urinary incontinence
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Cluster
Blinding
Open -no one is blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Behavior,custom |
Interventions/Control_1
An 8-week social media-based intervention
Interventions/Control_2
The control group began the intervention after an eight-week waiting period
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
-Women who aged 18 or older
-Women who have given their consent in electronically
Key exclusion criteria
-Women who currently receiving or have previously received treatment for urinary incontinence
-Women who undergoing treatment for urinary dysfunction or other concomitant diseases
-Women who undergoing or have undergone cancer or radiation therapy
-Pregnant women
-Postmenopausal women
-Women who considered unsuitable by the principal researcher
Target sample size
100
Research contact person
Name of lead principal investigator
| 1st name | Kaori |
| Middle name | |
| Last name | Kinouchi |
Organization
The University of Osaka Graduate school of Medicine, Division of Health Science
Division name
Department of Children and Women Health
Zip code
5650871
Address
1-7-B411, Yamadaoka Suita Osaka Japan
TEL
0668792537
kinouchi@sahs.med.osaka-u.ac.jp
Public contact
Name of contact person
| 1st name | Kaori |
| Middle name | |
| Last name | Kinouchi |
Organization
The University of Osaka Graduate school of Medicine, Division of Health Science
Division name
Department of Children and Women Health
Zip code
5650871
Address
1-7-B411, Yamadaoka Suita Osaka Japan
TEL
0668792537
Homepage URL
kinouchi@sahs.med.osaka-u.ac.jp
Sponsor or person
Institute
The University of Osaka
Institute
Department
Personal name
Funding Source
Organization
The University of Osaka
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
The University of Osaka Hospital Ethical Review Board
Address
CoMIT building 4th floor, 2-2, Yamadaoka Suita Osaka Japan
Tel
0662108296
rinri@hp-crc.med.osaka-u.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
| 2025 | Year | 09 | 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
Preinitiation
Date of protocol fixation
| 2025 | Year | 08 | Month | 13 | Day |
Date of IRB
Anticipated trial start date
| 2025 | Year | 10 | 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
Management information
Registered date
| 2025 | Year | 08 | Month | 13 | Day |
Last modified on
| 2025 | Year | 08 | Month | 13 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067218
