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RecruitingNCT07465354OCDtreatmentUpdated Sep 10, 2026

OCD Summer Treatment Program for Adolescents in Iceland

An interventional study of Intensive cognitive-behavioral treatment with exposure / response prevention in Obsessive-Compulsive Disorder (OCD), sponsored by University of Iceland. Recruiting at 1 site in Iceland. Open to participants aged 12 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-09-10.

Sponsored by University of Iceland · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Jun 2026; still recruiting 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Not applicable
Ages
12 Years to 18 Years
Sex
All
01

Study summary

The aim of the study is to examine the effectiveness of OCD treatment delivered in a group format for adolescents during a two week intensive summer treatment program.

Read the detailed description

The present study evaluates the effectiveness of the Icelandic adaptation of the Pediatric OCD Summer Program, originally developed by the British Columbia Children's Hospital in Vancouver, Canada. Specifically, it investigates the efficacy of this intensive intervention for Icelandic adolescents with OCD and their parents. The study also examines how executive functioning and emotion regulation may change over the course of treatment and influence outcomes, particularly among adolescents with co-occurring neurodevelopmental conditions such as ADHD and/or autism. The program will be implemented annually as an open clinical trial to accumulate a larger dataset and address these research questions comprehensively.

02

Conditions studied

  • Obsessive-Compulsive Disorder (OCD)

Keywords

  • Obsessive-compulsive disorder
  • Adolescents
  • intensive cognitive-behavioral treatment
  • Exposure and response prevention
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In context

Obsessive-Compulsive Disorder

635 studies on the registry are indexed under Obsessive-Compulsive Disorder; 166 are open to participants now.

This study's planned enrollment of 70 is above the median of 45 across 520 interventional studies indexed under Obsessive-Compulsive Disorder.

Browse Obsessive-Compulsive Disorder studies →

Lead sponsor

University of Iceland is the lead sponsor of 35 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
12 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • OCD diagnosis
  • Adolescents are fluent in Icelandic
  • Parents are fluent in Icelandic or English

Exclusion criteria

Exclusion Criteria:

  • Intellectual disability
  • Severe suicidal ideation
  • Schizophrenia
  • Severely impairing levels of autism
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
70 participants (estimated)

Study arms

  • Experimental
    Intensive group-based cognitive-behavioral treatment

    This cognitive-behavioral exposure / response prevention program is delivered intensively over two consecutive weeks, consisting of daily 2.5-hour sessions across 10 days. Each group includes 6-8 adolescents, with every participant paired with an individual therapist for each session, though therapists rotate daily. At the outset, adolescents receive workbooks and psychoeducation on the nature of obsessive thoughts and compulsive behaviors, along with strategies to manage symptoms and reduce impairment. The primary focus of the program is individualized exposure exercises conducted with a therapist during each session. Designed for adolescents aged 12-18, the program also includes parent sessions, in which parents learn to manage anxiety-driven behaviors at home and reduce family accommodation.

    Behavioral: Intensive cognitive-behavioral treatment with exposure / response prevention

Interventions

  • BehavioralIntensive cognitive-behavioral treatment with exposure / response prevention

    This cognitive-behavioral exposure / response prevention program is delivered intensively over two consecutive weeks, consisting of daily 2.5-hour sessions across 10 days. Each group includes 6-8 adolescents, with every participant paired with an individual therapist for each session, though therapists rotate daily. At the outset, adolescents receive workbooks and psychoeducation on the nature of obsessive thoughts and compulsive behaviors, along with strategies to manage symptoms and reduce impairment. The primary focus of the program is individualized exposure exercises conducted with a therapist during each session. Designed for adolescents aged 12-18, the program also includes parent sessions, in which parents learn to manage anxiety-driven behaviors at home and reduce family accommodation.

06

What researchers measure

Primary outcomes

  1. Behavioral Rating Inventory of Executive Function (BRIEF)

    A questionnaire designed to assess executive functioning in children and adolescents aged 5 to 18 years (Gioia et al., 2000). The questionnaire consists of 86 items with three response options: never = 1, sometimes = 2, and often = 3. A higher score on the BRIEF indicates greater executive functioning difficulties. The first 72 items are divided into eight clinical subscales that measure different aspects of executive function. These clinical subscales fall under two broader indices: the Behavioral Regulation Index (BRI) and the Metacognition Index (MI), which together form a Global Executive Composite (GEQ) score. The psychometric properties of the Icelandic version have proven to be acceptable.

    Time frame: Baseline, 1 week after treatment, 6 month follow-up, 12 month follow-up

  2. Children's Yale-Brown Obsessive Compulsive Scale (CY-BOCS)

    This is a semi-structured interview (Scahill et al., 1997) intended to assess the symptoms and severity of obsessive compulsive disorder in children and adolescents aged 6-17 years. The scores range from 0-40, a higher score indicating more OCD related impairment with a clinical cut-off score of 15. The interview is conducted either with both the child and parent present or, in some cases, separately. The interview method depends, among other things, on the child´s age and developmental level. This interview is widely used, both for clinical purposes and in research, and has been translated into many languages. Today, it is considered the gold standard for assessing the severity of OCD symptoms and treatment response and is the most commonly and widely accepted tool for such evaluations (Mataix-Cols et al, 2016; Skarphedinsson et al, 2017). The interview has demonstrated strong psychometric properties (Cook et al., 2015; Højgaard et al., 2017).

    Time frame: Baseline, 1 week after treatment, 6 month follow-up, 12 month follow-up

  3. The Child Obsessive-Compulsive Impact Scale (COIS-R)

    This is a 55-item questionnaire that assesses functional impairment due to OCD in the child's most important environments (home, school, and social situations) (Piacentini et al, 2007). Each question is rated on a Likert scale from 0-3 and a higher score indicates more OCD related impairment. The adolescents will complete the child/adolescent form and parents will complete the parent form.

    Time frame: Baseline, 1 week after treatment, 6 month follow-up, 12 month follow-up

  4. Revised Children 's Anxiety and Depression Scale (RCADS)

    This is a commonly used questionnaire to screen for anxiety and depressive disorders and to assess changes following an intervention. The RCADS is a 47-item questionnaire designed for parents and children (ages 8-17) and includes the following scales: Generalized Anxiety Disorder, Separation Anxiety Disorder, Social Anxiety Disorder, Panic Disorder, Obsessive-Compulsive Disorder, and Depressive Symptoms. Items are rated on a four-point scale and higher scores indicate more difficulties: 0 = never, 1 = sometimes, 2 = often, 3 = always. The Icelandic version has acceptable psychometric properties in both general and clinical populations.

    Time frame: Baseline, 1 week after treatment, 6 month follow-up, 12 month follow-up

Secondary outcomes

  1. Family Accommodation Scale for OCD- Self-Rated (FAS-SR)

    This is a 19-item scale developed to assess the extent to which the family attempts to accommodate the child´s symptoms to reduce distress. The scale is completed by parents and includes items such as how much the family tries to reassure the child, alter plans and activities, or help the child to avoid objects, places, or situations that cause distress. Scores range from 0-48 and higher scores indicate more family accommodation. The scale has acceptable psychometric properties, including internal consistency of 0.90 and high correlation with the standardized Family Accommodation Interview (Pinto et al., 2013).

    Time frame: Baseline, 1 week after treatment, 6 month follow-up, 12 month follow-up

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Study locations

1 of 1 sites recruiting
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References and documents

Publications

  • Selles RR, Belschner L, Negreiros J, Lin S, Schuberth D, McKenney K, Gregorowski N, Simpson A, Bliss A, Stewart SE. Group family-based cognitive behavioral therapy for pediatric obsessive compulsive disorder: Global outcomes and predictors of improvement. Psychiatry Res. 2018 Feb;260:116-122. doi: 10.1016/j.psychres.2017.11.041. Epub 2017 Nov 15. PubMed 29179016 ↗

Individual participant data

Plan to share: No — As the study includes repeated measures of a clinical child population, parts of the data will be classified as sensitive personal data and thus restricted by the permit from the National Bioethics Committee of Iceland.

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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jun 2026 (actual). Primary completion is estimated for Sep 2030, 51 months after the start.

Of 234 non-industry interventional studies with no phase under Obsessive-Compulsive Disorder, half reached primary completion within 43 months of starting (the median), counting those still running; a quarter within 22 and three quarters within 65. This study's planned 51 months is above that.

Counting every sponsor, half of 237 studies reached it within 43 months; a quarter within 22 and three quarters within 65.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 6, 2026
First posted
Mar 11, 2026
StartActual
Jun 1, 2026
Primary completionEst.
Sep 1, 2030
CompletionEst.
Sep 1, 2033
Last update
Sep 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07465354
Lead sponsor
University of Iceland
Responsible party
Sponsor
First posted
Mar 11, 2026
Start date
Jun 1, 2026
Primary completion
Sep 1, 2030 (estimated)
Completion
Sep 1, 2033 (estimated)
Last update
Sep 10, 2026

Study contacts

Dagmar Kr. Hannesdottir, PhD
Contact
dkh@hi.is
+354 525 4351

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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