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An investigation of longitudinal changes in the severity of symptoms based on behaviors, neuroimaging, and biosamples in children with developmental disorder centered on the child-parent relationships

An investigation of longitudinal changes in the severity of symptoms based on behaviors, neuroimaging, and biosamples in children with developmental disorder centered on the child-parent relationships - Child biobehavioral development study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000032859
Enrollment
60
Registered
2018-06-04
Start date
2018-06-04
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Children with developmental disorder, children at the high risk of developmental disorder, and their biological parents

Interventions

Children with developmental disorder Infants/children at high risk of developmental disorder Biological parents

Sponsors

Showa University
Lead Sponsor
National Center for Child Health and Development
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Infants/Children at high risk of developmental disorder (1) Infants/children who have brothers/sisters diagnosed as either of ASD or ADHD (2) Individuals who do not have any other neurological or psychiatric disorders (3) Infants/children whose guardians fully understand the contents of this study and gave the consent. Children with developmental disorder (1) Child who is diagnosed as either of ASD or ADHD (2) Individuals who do not have any other neurological or psychiatric disorders (3) Children whose guardians fully understand the contents of this study and gave the consent. Parents (1) Individuals who are the biological parents of children with developmental disorders and at the high risk of developmental disorder (2) Individuals who do not have any other neurological or psychiatric disorders (3) Individuals who have capability of informed consent

Exclusion criteria

Exclusion criteria: 1) with implanted cardiac pacemaker 2) with surgical aneurysm clips 3) with neurostimulator 4) with implanted pumps 5) with metal fragments in body 6) with tattoos, permanent eyeliner (if ink contains metallic specks)

Design outcomes

Primary

MeasureTime frame
Neuroimaging, genetic information, and behavioral data

Secondary

MeasureTime frame
Psychological tests, questionnaires

Countries

Japan

Contacts

Public ContactTakashi Itahashi

Showa University Medical Institute of Developmental Disabilities Research

ita3@med.showa-u.ac.jp03-3300-5231

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026