Topic: Mental Health
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The inclusion criteria have been designed to be consistent with previous OCD DBS studies and to ensure that patients have not responded in a useful and sustained manner to either modifications of medication or any form of CBT 1. Patients must have undergone intensive treatment and have demonstrable treatment resistance as defined by: 1.1. At least two SRIs for a minimum of 12 weeks at optimal British National Formulary (BNF) doses 1.2.Augmentation of SRI treatment with antipsychotic drugs administered at maximally tolerated doses or by extending the SSRI dose beyond BNF limits 1.3. Two trials of CBT of at least 10 hours 1.4. Failed inpatient treatment 2. Patients must also satisfy the following criteria: 2.1. Age > 20 years 2.2. Confirmation of a primary diagnosis of obsessive compulsive disorder (ICD10 F42.0—F42.9) 2.3. Duration of illness of at least 10 years 2.4. At least 2 years of unremitting symptoms despite intensive psychopharmacological and psychological treatment or failure to sustain, over a 3 month period, a response to inpatient psychological treatment by at least 33% with accompanying optimised pharmacological therapy 2.5. A minimum score of 32 on Yale Brown Obsessive Compulsive Scale (YBOCS 22) thus constituting profound illness and a maximum score of 50 on the DSM IV General Assessment of Function Scale (GAF) 2.6. Ability to provide sustained informed consent
Exclusion criteria
Exclusion criteria: 1. Current diagnoses of substance misuse (ICD10 F10—F19), organic brain syndrome (ICD10 F00—F09), adult personality disorder (ICD10 F60—F69), pervasive developmental disorder (ICD10 F84); schizophrenia (ICD10 F20-F29) and bipolar disorder (ICD 10 F30-31) 2. Contraindications to neurosurgery 3. Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| YBOCS improvement greater than or equal to 35%; Timepoint(s): 15 months | — |
Countries
United Kingdom