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A randomized controlled trial of Family based ERP Program (FERP) for obsessive compulsive disorder

A randomized controlled trial of Family based ERP Program (FERP) for obsessive compulsive disorder - FERP Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021763
Enrollment
36
Registered
2016-04-11
Start date
2016-04-15
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 based ERP Program in addition to treatment as usual treatment as usual

Sponsors

FERP study group, National Center of Cognitive Behavior Therapy and Research, National Center of Neurology and Psychiatry
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (OCD patient) 1. Subjects with primary diagnosis of obsessive compulsive disorder by DSM-IV. 2. Subjects with Y-BOCS>=8 3. Aged 20 years or older, and younger than 65 years at screening. 4. Subjects who give consent with not to change current pharmacotherapy except for symptom improvement. 5. Subjects who have the possibility of going to the hospital more than 12 times during the study period. 6. Subjects who give full consent in the participation of the study. (Patient's family) 1. Subjects with whom the patient lives at one hour daily. 2. Subjects with whom the patient has identified as the family member who is most involved the OCD. 3. Subjects who have the possibility of going to the hospital 8 times during the study period. 4. 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 DIM-IV Axis I Disorders at screening. 3. No serious suicidal ideation at screening. 4. No treatment of individual CBT for OCD. 5. No major cognitive deficits at screening. 6. No severe or unstable medical co-morbidities at screening. 7. Other relevant reason decided by the FERP principal investigator.

Design outcomes

Primary

MeasureTime frame
Yale-Brown Obsessive Compulsive Scale(Y-BOCS) score at the time of end of intervention period

Secondary

MeasureTime frame
1.Family Accommodation Scale for Obsessive Compulsive Disorder: FAS 2.OCD Family Functioning Scale: OFF 3.Beck Depression Inventory: BDI 4.Sheehan Disability Scale: SDS 5.Kessler Psychological Distress Scale-6: K6 6.Euro QOL: EQ5D 7.Patient Global Impression-severity scale: PGI-S / Patient Global Impression-improvement scale: PGI-I

Countries

Japan

Contacts

Public ContactYuki Kobayashi

National Center of Neurology and Psychiatry National Center for Cognitive Behavior Therapy and Research

ykobayashi@ncnp.go.jp042-341-2711

Outcome results

None listed

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