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Cognitive Behavioral Therapy for Anger in Patients with Traumatic Brain Injury

Cognitive Behavioral Therapy for Anger in Patients with Traumatic Brain Injury - CBT for TBI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038222
Enrollment
36
Registered
2019-12-01
Start date
2020-10-01
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

traumatic brain injury

Interventions

Group cognitive behavioral therapy based on the manual focusing instantaneous and long-term control of anger, which is held 6 sessions of 90 minutes for 3-6 patients a week

Sponsors

Keio University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subject who meet all of the following conditions are eligible to participate in this study. (1) 20 to 65 years old (2) Subjects with traumatic brain injury due to head injury or organic brain diseases (3) subjects feeling difficulties in management of anger (4) Understand the purpose and content of this study and express written consent to participate in this study based on own will

Exclusion criteria

Exclusion criteria: Subjects with any of the following conditions are excluded from this study. (1) History of psychotic disorders such as mood disorders, schizophrenia and alcohol / substance use disorders (2) Subjects who will be impossible to continue visiting hospitals because of move and so on (3) Subjects who have a life-threatening or unstable physical, brain, or mental illness in clinical diagnosis (4) Subjects who have symptoms interfering with group psychotherapy, such as significant memory impairment, intellectual disability or suicidal idea/acts (5) Others that the Principal Investigator has determined to be inappropriate for this research

Design outcomes

Primary

MeasureTime frame
Improvement rate of State-Trait Anger Expression Inventory-II (STAXI-II) score among baseline and 0/3 months after treatment

Secondary

MeasureTime frame
Improvement rate of Patient Health Questionnaire-9, Generalized Anxiety Disorder 7-item, Quality of Life after Brain Injury, and Frontal Systems Behavior Scale amongbaseline and 0/3 months after treatment

Countries

Japan

Contacts

Public ContactToshiaki Kikuchi

Keio University School of Medicine Department of Neuropsychiatry

t-kick@nifty.com03-5363-3971

Outcome results

None listed

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