UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000050196 |
|---|---|
| Receipt number | R000057169 |
| Scientific Title | Study of related factors in symptoms of adult attention-deficit/hyperactivity disorder |
| Date of disclosure of the study information | 2023/02/01 |
| Last modified on | 2025/02/03 09:22:12 |
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Basic information
Public title
Study of related factors in symptoms of adult attention-deficit/hyperactivity disorder
Acronym
Study of related factors in adult ADHD
Scientific Title
Study of related factors in symptoms of adult attention-deficit/hyperactivity disorder
Scientific Title:Acronym
Study of related factors in symptoms of adult ADHD
Region
| Japan |
Condition
Condition
adult attention-deficit/hyperactivity disorder
Classification by specialty
| Psychiatry | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The primary purpose is to compare the influence of factors such as parental care attitudes, attachment, and ADHD symptoms in childhood on the presence or absence of ADHD symptoms in adults. A secondary purpose is to examine the relationship between these factors and factors such as depression and busyness.
Basic objectives2
Others
Basic objectives -Others
Investigation of factors affecting the development of ADHD symptoms
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
The primary endpoint is the difference in the effects of the WURS score, ECR-GO score, and PBI score on the presence or absence of adult ADHD symptoms.
Key secondary outcomes
Secondary endpoints are comparisons and studies of relationships among measures such as ASRS score, WURS score, ECR-GO score, PBI score, PHQ-9 score, and busyness questionnaire scores.
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
| 100 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
(1) Those who understand the purpose of the research and can obtain written consent to participate in the research.
(2) Those who are 18 years old or older at the time of study participation.
Key exclusion criteria
None
Target sample size
1000
Research contact person
Name of lead principal investigator
| 1st name | Hisae |
| Middle name | |
| Last name | Ono |
Organization
Kwansei Gakuin University
Division name
Department of Integrated Psychological Sciences, School of Humanities
Zip code
662-8501
Address
1-155 Uegahara Ichibancho, Nishinomiya, Hyogo
TEL
0798544517
hisaono@kwansei.ac.jp
Public contact
Name of contact person
| 1st name | Hisae |
| Middle name | |
| Last name | Ono |
Organization
Kwansei Gakuin University
Division name
Department of Integrated Psychological Sciences, School of Humanities
Zip code
662-8501
Address
1-155 Uegahara Ichibancho, Nishinomiya, Hyogo
TEL
0798544517
Homepage URL
hisaono@kwansei.ac.jp
Sponsor or person
Institute
Kwansei University
Institute
Department
Personal name
Funding Source
Organization
Kwansei University
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
Ethics Committee for Life Science and Medical Research Involving Human Subjects
Address
Gakuen Uegahara 1 ban Sanda, Hyogo
Tel
0795659052
med-ethic@kwansei.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
| 2023 | Year | 02 | Month | 01 | Day |
Related information
URL releasing protocol
Publication of results
Published
Result
URL related to results and publications
https://www.jstage.jst.go.jp/article/jjpm/advpub/0/advpub_2024003/_pdf/-char/ja
Number of participants that the trial has enrolled
1017
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
Main results already published
Date of protocol fixation
| 2023 | Year | 01 | Month | 26 | Day |
Date of IRB
| 2023 | Year | 01 | Month | 26 | Day |
Anticipated trial start date
| 2023 | Year | 01 | Month | 31 | Day |
Last follow-up date
| 2026 | Year | 03 | Month | 30 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Online cross-sectional research
Management information
Registered date
| 2023 | Year | 01 | Month | 31 | Day |
Last modified on
| 2025 | Year | 02 | Month | 03 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000057169
