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ordic Long-term Obsessive compulsive disorder (OCD) Treatment Study

Not Applicable
Completed
Conditions
Obsessive compulsive disorder
Mental and Behavioural Disorders
Registration Number
ISRCTN66385119
Lead Sponsor
The Centre for Child and Adolescent Mental Health, Eastern and Southern Norway (R.BUP) (Norway)
Brief Summary

2014 Results article in http://www.ncbi.nlm.nih.gov/pubmed/25358486 results 2015 Results article in http://www.ncbi.nlm.nih.gov/pubmed/25721185 results 2019 Results article in https://www.ncbi.nlm.nih.gov/pubmed/31622874 results (added 21/04/2020) 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33861384/ (added 19/04/2021) 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/33881628/ quality of life results (added 22/04/2021) 2023 Results article in https://pubmed.ncbi.nlm.nih.gov/38070870/ Relapse rates following remission (added 11/12/2023)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
269
Inclusion Criteria

1. Patients 7 - 17 years of age
2. Moderate-severe obsessive compulsive disorder according to Diagnostic and Statistical Manual of Mental Disorders - Fourth Edition (DSM IV). Severity is defined by Children's Yale-Brown Obsessive Compulsive Scales (CY-BOCS) scores of 16 or above

Exclusion Criteria

1. Co-morbidity has not higher treatment priority (e.g. psychosis, anorexia nervosa, severe depression with suicidality, an autistic disorder or Asperger's syndrome)
2. Pervasive developmental disorders (PDD) not otherwise specified (NOS) is allowed if Clinical Global Impression (CGI) score for the PDD is less than or equal to 3 and CGI for the PDD NOS is less than or equal to CGI for the OCD
3. Mental retardation (intelligence quotient [IQ] less than 70)
4. Patients have not been treated with selective serotonin reuptake inhibitor (SSRI) or CBT for their OCD during the last year
5. If the patient is of non-Nordic ethnicity both the patient and one parent must speak a Nordic language

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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