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Structural and functional magnetic resonance imaging (sMRI, fMRI) study of children and adolescents with reactive attachment disorder (RAD)

Structural and functional magnetic resonance imaging (sMRI, fMRI) study of children and adolescents with reactive attachment disorder (RAD) - MRI study of RAD

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014655
Enrollment
60
Registered
2014-07-26
Start date
2013-03-22
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Reactive Attachment Disorder

Interventions

Patients with RAD Normal controls Patients with ADHD

Sponsors

University of Fukui, Research Center for Child Mental Development, Division of Psychosocial Support for Nurturing
Lead Sponsor
Aichi Children&#39
Collaborator
s Health and Medical Center National Institute for Physiological Sciences RIKEN Center for Life Science Technologies
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients with reactive attachment disorder based on the classifications in the diagnostic and statistical manual of mental disorders (DSM-IV-TR). Healthy children and adolescents with higher level of IQ 70. 2) Subjects within the age range of 7-18 years old. 3) Must demonstrate an acceptable degree of compliance with medication and procedures in the opinion of the investigator.

Exclusion criteria

Exclusion criteria: 1) Subjects who have any other current DSM-IV-TR diagnosis of the following; "Pervasive development disorder", "Attention-deficit/hyperactivity disorder","Schizophrenia and Other Psychotic Disorders","Delirium, Dementia, and Amnestic and Other Cognitive Disorders", "Substance-Related Disorders","eating disorders","personality disorders". 2) Subjects who have a diagnosis of a severe physical disorder. 3) Subjects who are planned for an immediate therapeutic plan change due to unstable physical or psychological symptoms. 4) Subjects with metalic device in their body. 5) Subjects who, in the Investigator's opinion, might not be suitable for the study.

Design outcomes

Primary

MeasureTime frame
sMRI and fMRI analysis: brain structure and function with MRI during resting state/cognitive task.

Secondary

MeasureTime frame
Neuropsychological test

Countries

Japan

Contacts

Public ContactAkemi Tomoda

University of Fukui, Research Center for Child Mental Development Division of Psychosocial Support for Nurturing

atomoda@u-fukui.ac.jp0776-61-8677

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026