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Effectiveness of Family Inclusive Treatment program for OCD adolescents : Before-after trial

Effectiveness of Family Inclusive Treatment program for OCD adolescents : Before-after trial - Effectiveness of Family Inclusive Treatment program for OCD adolescents : Before-after trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038215
Enrollment
12
Registered
2019-10-07
Start date
2019-10-10
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

Obsessive Compulsive Disorder

Interventions

Family Inclusive treatment program in addition to treatment as usual

Sponsors

Kanazawa University Department of Psychiatry and Neurobiology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: OCD patient 1.Subjects with primary diagnosis of obsessive compulsive disorder by DSM-5. 2.Those who have 16 or more CY-BOCS 3.Aged 12 years or older, and younger than 17 years at screening. 4.Subjects who give consent with not to change current pharmacotherapy. 5.Subjects who give full consent in the participation of the study. Patient's family 1. One family member living with the patient for at least one year at the time of screening. The family members are primarily responsible for childcare or are most involved in patient OCD. 2. Subjects who give full consent in the participation of the study.

Exclusion criteria

Exclusion criteria: 1.No alcohol or substance use disorder in 6 months prior to the screening. 2.No other primary Disorders in 6 months prior to the screening. 3.No serious suicidal ideation at screening. 4.Patients with IQ less than 70 5.Persons who have adjusted their drugs for 12 weeks before screening 6.Patients who are difficult to visit 14 times after screening 7.Patients whose family members are difficult to participate in all five family program sessions during CBT 8.Those who have received CBT for structured obsessive-compulsive disorder by the time of screening 9.Those who have severe cognitive impairment that makes it difficult to perform CBT at the time of screening 10.Those who have a serious or unstable physical disease that is life-threatening in clinical diagnosis at the time of screening 11.Those who are deemed inappropriate by the research supervisor

Design outcomes

Primary

MeasureTime frame
CY-BOCS;Child Yale Brown Obsessive Compulsive Scale at the time of end of intervention period

Secondary

MeasureTime frame
1.FAS;Family Accommodation Scale 2.OFF;OCD Family Functioning Scale 3.CGI-S;Impairment 4.CGI-S;Improvement 5.CBCL;Child Behavior Checklist, YSR;Youth Self-Report

Countries

Japan

Contacts

Public ContactKeiko Kontani

Kanazawa University Department of Psychiatry and Neurobiology

cbt_fit@yahoo.co.jp076-265-2304

Outcome results

None listed

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