Study Results
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Basic Information
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COMPLETED
NA
178 participants
INTERVENTIONAL
2019-03-02
2025-06-25
Brief Summary
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In many countries including DK, CBT is the recommended, first-line treatment for OCD. All individuals who seek treatment in the Danish Regions are offered CBT. However, reviews show that up to 50% of patients either do not respond to CBT or terminate treatment prematurely. Despite this large number of non-responders, no significant progress for OCD treatment has been made since initial efficacy trials. Alternatives to CBT are needed .
Acceptance and Commitment therapy (ACT) is an innovative psychotherapy that can potentially help individuals with OCD who do not benefit from CBT. ACT targets the habitual thinking and behaviors that mark OCD by aiming to increase value-based behavior. OCD often co-occurs with depression and other anxiety disorders making treatment more difficult. ACT is a transdiagnostic treatment targeting symptoms that are common to anxiety and mood disorders. Preliminary findings indicate that ACT may be an effective treatment for OCD. However, these findings constitute a low level of evidence. Before ACT can be declared as an effective treatment for OCD, it needs to be demonstrated in randomize controlled trials, in which ACT is compared to legitimate, active treatments, such as CBT. This project will test the effectiveness of group-based ACT by comparing it to the first-line treatment, group-CBT in 180 participants referred for treatment in a specialized outpatient clinic at the Mental Health Services, Capital Region of Denmark. Furthermore, moderators and predictors of treatment response will be investigated.
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Detailed Description
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What treatment works for whom? Another crucial step in order to improve the treatment for OCD is to consider individual patient characteristics in the composition of optimal treatment setups facilitating personalized treatment. This requires extensive knowledge of predictors and moderators of OCD treatment success. However, to date no reliable predictors or moderators have been identified. Previous predictor and moderator studies have suggested that attachment patterns and anxiety sensitivity may be related to treatment outcome for ACT and CBT. Accumulating studies also highlights the relevance of investigating biological markers in relation to OCD. However, very little is known about the role of biomarkers in OCD and in psychotherapy although studies are emerging.
Purpose This study aims to test the (long-term) effectiveness of ACT for OCD and to compare the effectiveness to CBT in a naturalistic clinical setting. Additionally, the aim is to identify reliable markers to guide efficient treatment choice by examining several theory-driven, putative predictors and moderators: 1) moderators which are theoretically connected to the two treatments (e.g. thought-action-fusion, anxiety sensitivity) 2) personality and interpersonal characteristics involved in the maintenance of OCD (e.g. emotion regulation, attachment style, personality traits) and 3) biomarkers known to be associated with comorbidity, chronicity and treatment refractivity. Finally, 4) the study will investigate the moderating effects of clinical and demographic characteristics (e.g. comorbid depression, gender, education, age). Main hypotheses 1: In the overall sample, both the ACT and CBT treatment will yield clinically significant results, indicated by a change in Yale-Brown Obsessive Compulsive Scale (Y-BOCS) scores from pre- to posttreatment, with ACT and CBT being equally effective. 2: The effect at 6- and 12-months follow-up will be equal for ACT and CBT, measured with Y-BOCS. 3: Participants with comorbid depression at baseline will benefit more from ACT than CBT. Method The study is a single blinded, pragmatic, non-inferiority, parallel, multi-center block randomized controlled trial of ACT vs CBT for OCD. In total, 180 patients are recruited from two regional MHS centers across Capital Region of Denmark and included in two intervention arms. The participants will be assessed with diagnostic interview and self-report measures at baseline, post-treatment, 6-months and 12-months follow-up. Randomization The randomization will be carried out based on an allocation list with permuted blocks using the Region´s secure system REDcap by a person not attached to the project.
Data analysis
Longitudinal data will be analyzed using Mixed Model Repeated Measures (MMRM) and Hierarchical Linear Modeling (HLM) and an intend-to-treat sample including all randomized participants. Detection of the moderating value of the proposed variables will be analyzed in the two domains, using the method proposed by Kraemer. The possible moderators will be examined for individual effect sizes and then entered into a forward-stepwise regression model predicting differential treatment response. K-fold cross validation will be used to identify the number of variables to be included in the final moderator model in order to identify moderators in rank-order. Timeplan The project is planned to start in January 2019 and will run over 4 years.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Cognitive behavioral therapy
Manualized group-based cognitive behavioual therapy delivered by clinical psychologists and psychiatrists. The treatment consists of 14 sessions of each 2 hours.
Cognitive behavioral therapy
Group based psychotherapy
Acceptance and commitment therapy
Manualized group-based Acceptance and Commitment therapy delivered by clinical psychologists and psychiatrists. The treatment consists of 14 sessions of each 2 hours.
Acceptance and commitment therapy
Group based psychotherapy
Interventions
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Cognitive behavioral therapy
Group based psychotherapy
Acceptance and commitment therapy
Group based psychotherapy
Eligibility Criteria
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Inclusion Criteria
* are between 18-65 years
* are free of alcohol and substance abuse
* are not receiving any other psychotherapy during the study
* are medication-free or stabilized on psychotropic medication
* speak and understand Danish
* provide written consent
18 Years
65 Years
ALL
No
Sponsors
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Rigshospitalet, Denmark
OTHER
Responsible Party
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Sara Kerstine Kaya Nielsen
Postdoctoral Researcher
Locations
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University Hospital Copenhagen
Copenhagen, , Denmark
Countries
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Other Identifiers
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VD-2018-376
Identifier Type: -
Identifier Source: org_study_id
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