UMIN-CTR Clinical Trial

Basic information
Public title	Estimation of Depression Risk Using Assessment of Caregiver Burden in Primary Caregivers of Persons Requiring Care at Home
Acronym	Estimation of Depression Risk Using Assessment of Caregiver Burden in Primary Caregivers of Persons Requiring Care at Home
Scientific Title	Estimation of Depression Risk Using Assessment of Caregiver Burden in Primary Caregivers of Persons Requiring Care at Home
Scientific Title:Acronym	Estimation of Depression Risk Using Assessment of Caregiver Burden in Primary Caregivers of Persons Requiring Care at Home
Region	Japan

Condition
Condition	Persons requiring nursing care at home who are using some type of nursing care service and their primary caregivers.
Classification by specialty	Rehabilitation medicine
Classification by malignancy	Others
Genomic information	NO

Objectives
Narrative objectives1	To examine whether it is possible to discriminate the risk of depression among primary caregivers and to stratify them according to the degree of risk, based on the quantitative assessment of caregiver burden and the basic information of primary caregivers and persons requiring care at home.
Basic objectives2	Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes	Basic attributes of the primary caregiver Basic attributes of primary caregiver Health status of primary caregiver
Key secondary outcomes

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	Not applicable
Age-upper limit	Not applicable
Gender	Male and Female
Key inclusion criteria	Persons requiring nursing care at home who are using some type of nursing care service and their primary caregivers.
Key exclusion criteria	When the person requiring care at home and the primary caregiver live separately and the person lives alone. If the primary caregiver has difficulty answering the questionnaire due to cognitive function or mental state problems. When consent to participate in this study cannot be obtained.
Target sample size	100

Research contact person
Name of lead principal investigator	1st name Tomohisa Middle name Last name Chibana
Organization	Kawaguchi Neurosurgery Rehabilitation Clinic
Division name	Rehabilitation department
Zip code	5730086
Address	9-25-202, Karien-cho, Hirakata-shi, Osaka
TEL	0728351010
Email	kawaguchi.ns.reha@gmail.com

Public contact
Name of contact person	1st name Tomohisa Middle name Last name Chibana
Organization	Kawaguchi Neurosurgery Rehabilitation Clinic
Division name	Rehabilitation department
Zip code	5730086
Address	9-25-202, Karien-cho, Hirakata-shi, Osaka
TEL	0728351010
Homepage URL
Email	kawaguchi.ns.reha@gmail.com

Sponsor
Institute	Kawaguchi Neurosurgery Rehabilitation Clinic
Institute
Department

Funding Source
Organization	None
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	Kawaguchi Neurosurgery Rehabilitation Clinic
Address	9-25-202, Karien-cho, Hirakata-shi, Osaka
Tel	0728351010
Email	kawaguchi.ns.reha@gmail.com

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	2021 Year 10 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	Open public recruiting
Date of protocol fixation	2021 Year 10 Month 16 Day
Date of IRB	2021 Year 10 Month 15 Day
Anticipated trial start date	2021 Year 10 Month 16 Day
Last follow-up date	2022 Year 12 Month 31 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information	None

Management information
Registered date	2021 Year 10 Month 16 Day
Last modified on	2021 Year 10 Month 16 Day

Link to view the page
URL(English)	https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000052254