UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000059044 |
|---|---|
| Receipt number | R000067530 |
| Scientific Title | The effects of a work-life crafting intervention program on well-being of female workers: a pretest-posttest study |
| Date of disclosure of the study information | 2025/09/10 |
| Last modified on | 2025/09/10 13:53:47 |
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Basic information
Public title
The effects of a work-life crafting intervention program
Acronym
The effects of a work-life crafting intervention program
Scientific Title
The effects of a work-life crafting intervention program on well-being of female workers: a pretest-posttest study
Scientific Title:Acronym
The effects of a work-life crafting intervention program on well-being of female workers: a pretest-posttest study
Region
| Japan |
Condition
Condition
N/A
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The aim of this study is to investigate the effect of a work-life crafting intervention program on well-being of female workers using a pretest-posttest study design.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Well-being (WHO5) (Immediately after intervention, 3 months after intervention)
Key secondary outcomes
Japanese version of the Survey Work-Home Interaction-NijmeGen, the SWING (SWING-J)
Work-self balance(negative) (The New Brief Job Stress Questionnaire)
Work-self balance(positive) (The New Brief Job Stress Questionnaire)
Psychological distress(The Brief Job Stress Questionnaire)
Work engagement(UWES)
Work performance(WHO-HPQ)
Implementation outcome (iOSDMH)
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Uncontrolled
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Behavior,custom |
Interventions/Control_1
This program consists of two sessions that provide psychoeducation on work-life crafting
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
1) Adults aged 18 years or older
2) Women
3) Workers
Key exclusion criteria
N/A
Target sample size
70
Research contact person
Name of lead principal investigator
| 1st name | Asuka |
| Middle name | |
| Last name | Sakuraya |
Organization
Graduate School of Medicine, The University of Tokyo
Division name
Department of Digital Mental Health
Zip code
113-0033
Address
7-3-1, Hongo, Bunkyo-ku, Tokyo
TEL
03-5800-9621
asuka@m.u-tokyo.ac.jp
Public contact
Name of contact person
| 1st name | Asuka |
| Middle name | |
| Last name | Sakuraya |
Organization
Graduate School of Medicine, The University of Tokyo
Division name
Department of Digital Mental Health
Zip code
113-0033
Address
7-3-1, Hongo, Bunkyo-ku, Tokyo
TEL
03-5800-9621
Homepage URL
asuka@m.u-tokyo.ac.jp
Sponsor or person
Institute
Graduate School of Medicine, The University of Tokyo
Institute
Department
Personal name
Funding Source
Organization
Pasona Safety Net Inc.
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Research Ethics Committee, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo
Address
7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, JAPAN
Tel
03-5841-0818
ethics@m.u-tokyo.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 | 10 | 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
| 2025 | Year | 03 | Month | 01 | Day |
Date of IRB
| 2025 | Year | 08 | Month | 27 | Day |
Anticipated trial start date
| 2025 | Year | 08 | Month | 29 | Day |
Last follow-up date
| 2026 | Year | 01 | Month | 30 | 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 | 09 | Month | 10 | Day |
Last modified on
| 2025 | Year | 09 | Month | 10 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067530
