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Enhanced cognitive behavioral therapy for children and adolescents with obsessive compulsive disorder: an open trial

Acceptability and feasibility of enhanced cognitive behavioral therapy (eCBT) for children and adolescents with obsessive compulsive disorder: an open trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN37530113
Enrollment
70
Registered
2020-01-31
Start date
2017-09-04
Completion date
Unknown
Last updated
2021-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric OCD Mental and Behavioural Disorders Obsessive-compulsive disorder

Interventions

Current interventions as of 11/06/2020: Until 16 March 2020, all participants received enhanced cognitive behavioral therapy (eCBT) for pediatric OCD. eCBT consists of the usual, evide

Sponsors

Central Norway Regional Health Authority
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age 7–17 years (inclusive) 2. A primary DSM 5 diagnosis of obsessive-compulsive disorder 3. CY-BOCS = 16

Exclusion criteria

Exclusion criteria: 1. A psychiatric comorbidity that has a higher treatment priority than OCD, and makes participation clinically inappropriate (for example, primary anorexia nervosa, depression with suicidality that requires acute treatment, and psychosis) 2. (Estimated) IQ below 70 3. Insufficient understanding of the Norwegian or English language

Design outcomes

Primary

MeasureTime frame
1. Acceptability assessed using Client Satisfaction Questionnaire (CSQ-8), child and parent version post-treatment 2. Feasibility: preterm treatment drop-out measured post-treatment 3. Effectiveness assessed using the Children’s Yale-Brown Obsessive Compulsive Scale (CY-BOCS) administered by a blind rater (blinded for treatment phase) pre- and post-treatment, and at 3 and 6 months follow-up

Secondary

MeasureTime frame
Acceptability assessed using: 1. Treatment evaluation questionnaire (child and parent version) composed of the User Experience Questionnaire and (self-developed) treatment-specific questions, measured post-treatment 2. Barriers to Treatment Participation Scale (BTPS). For the aim of the present study the researchers shortened the questionnaire and added a child version. Measured post-treatment. Effectiveness assessed using: 1. K-SADS-Pl at pre- and post-treatment 2. Child Obsessive-Compulsive Impact Scale (COIS-R): child and parent version at pre- and post-treatment, 3 and 6 months follow-up 3. Family Accommodation Scale for OCD – Self-Rated Version (FAS-SR): parents at pre- and post-treatment, 3 and 6 months follow-up 4. Strengths and Difficulties Questionnaire (SDQ): child and parent version at pre- and post-treatment, 3 and 6 months follow-up 5. Child Behavior Checklist (CBCL): parents at pre- and post-treatment, 6 months follow-up 6. Youth Self-Report Questionnaire (YSR): children 11 years and older at pre- and post-treatment, 6 months follow-up 7. Screen for Child Anxiety Related Emotional Disorders (SCARED): child and parent version at pre- and post-treatment, 3 and 6 months follow-up 8. Mood and Feelings Questionnaire (MFQ): child and parent version at pre- and post-treatment, 3 and 6 months follow-up 9. KINDL: child and parent version at pre- and post-treatment, 3 and 6 months follow-up 10. Children’s Global Assessment Scale (CGAS) at pre- and post-treatment, 3 and 6 months follow-up 11. Clinical Global Impressions-Severity (CGI-S) at pre- and post-treatment, 3 and 6 months follow-up 12. Clinical Global Impressions Improvement (CGI–I) at post-treatment, 3 and 6 months follow-up 13. The Trimbos/iMTA Questio

Countries

Norway

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 17, 2026