Internet-based vs Face-to-face Cognitive Behavioural Therapy for Obsessive-compulsive Disorder
NCT02541968 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120
Last updated 2022-04-22
Summary
Randomized controlled non-inferiority trial comparing therapist-guided Internet-based Cognitive behavioral therapy (ICBT), self-guided ICBT, and individual face-to-face (f2f) CBT for Obsessive-Compulsive Disorder (OCD) in adults.
The primary objective is to evaluate whether ICBT is a non-inferior treatment option compared to the best possible available treatment for OCD, individual face to face (f2f) CBT. A second objective is to compare the efficacy of self-guided vs. therapist-guided ICBT. As this question has cost implications for the health system, a third objective is to carry out a health economic evaluation of both forms of ICBT, in relation to the gold standard f2f CBT. A fourth objective is to explore whether ICBT is equally suited for clinic-referred cases compared to self-referred patients. Finally, a fifth objective is to investigate whether genetic markers, in combination with clinical variables, can be employed to predict treatment outcomes with CBT in general.
Research Questions:
Q1: Is therapist-guided internet-based CBT (ICBT) for OCD non-inferior to face-to-face (f2f) CBT with regard to OCD symptoms, function and quality of life?
Q2: Is entirely self-guided ICBT non-inferior to f2f CBT with regard to OCD symptoms, function and quality of life?
Q3: Is ICBT a cost-effective treatment, compared to f2f CBT?
Q4: Is there a difference in treatment outcome between self-referred and clinical referred patients?
Q5: Can clinical variables and genetic markers be useful to predict which patients will benefit from CBT?
Conditions
- Obsessive-compulsive Disorder
Interventions
- BEHAVIORAL
-
Cognitive-behavioral therapy (face-to-face)
- BEHAVIORAL
-
Internet-based Cognitive-behavioral therapy
With therapist support
- BEHAVIORAL
-
Internet-based Cognitive-behavioral therapy without therapist support
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Christian Rück · Karolinska Institutet
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-09-03
- Primary Completion
- 2019-05-31
- Completion
- 2021-01-31
Countries
- Sweden
Study Locations
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