UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000053505
Receipt number R000061068
Scientific Title Effectiveness of mobile applications to Improve Insomnia Symptoms in Female Worker: A Systematic Review and Meta-Analyses
Date of disclosure of the study information 2024/02/01
Last modified on 2024/02/01 08:53:58

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Basic information

Public title

Effectiveness of mobile applications to Improve Insomnia Symptoms in Female Worker: A Systematic Review and Meta-Analyses

Acronym

Effectiveness of mobile applications to Improve Insomnia Symptoms in Female Worker: A Systematic Review and Meta-Analyses

Scientific Title

Effectiveness of mobile applications to Improve Insomnia Symptoms in Female Worker: A Systematic Review and Meta-Analyses

Scientific Title:Acronym

Effectiveness of mobile applications to Improve Insomnia Symptoms in Female Worker: A Systematic Review and Meta-Analyses

Region

Japan


Condition

Condition

Healthy women

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify if mobile sleep applications can alleviate insomnia symptoms among adult females.

Basic objectives2

Others

Basic objectives -Others

Not applicable

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

insomnia symptoms

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


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

65 years-old >

Gender

Male and Female

Key inclusion criteria

1. general population including women
2. those with insomnia symptoms
3. sleep digital application

Key exclusion criteria

1. other than original articles
2. those whose outcome is not insomnia symptoms
3. the subject is a child (less than 18 years) or older adult (more than 65 years)
4. the study is conducted on outpatients or inpatients
6. only male subjects

Target sample size

10000


Research contact person

Name of lead principal investigator

1st name Kyoko
Middle name
Last name Nomura

Organization

Akita University

Division name

Department of Environmental Health Science and Public Health, Graduate School of Medicine

Zip code

010-8543

Address

1-1-1, Hondo, Akita-shi, Akita

TEL

018-884-0687

Email

knomura@med.akita-u.ac.jp


Public contact

Name of contact person

1st name Songee
Middle name
Last name Jung

Organization

Akita University

Division name

Department of Environmental Health Science and Public Health, Graduate School of Medicine

Zip code

010-8543

Address

1-1-1, Hondo, Akita-shi, Akita

TEL

018-884-0688

Homepage URL


Email

jonsoni@med.akita-u.ac.jp


Sponsor or person

Institute

Akita University

Institute

Department

Personal name



Funding Source

Organization

Japan Agency for Medical Research and Development

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Department of Environmental Health Science and Public Health, Akita University Graduate School of Medicine

Address

1-1-1, Hondo, Akita-shi, Akita

Tel

018-884-6461

Email

soken@hos.akita-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

2024 Year 02 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

10290

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

No longer recruiting

Date of protocol fixation

2023 Year 03 Month 25 Day

Date of IRB

2023 Year 06 Month 27 Day

Anticipated trial start date

2023 Year 06 Month 30 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

The systematic review has adhered to the guidelines in PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-analyses) for both the search process and reporting procedures. Electronic databases such as PubMed, Cochrane, PsycINFO, and Web of Science will be used.


Management information

Registered date

2024 Year 02 Month 01 Day

Last modified on

2024 Year 02 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000061068


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name