iCBT for Adult Obsessive-Compulsive Disorder

NCT ID: NCT07081438

Last Updated: 2025-07-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-09-01

Study Completion Date

2027-03-01

Brief Summary

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The goal of the study is to assess the feasibility, acceptability, and potential effects of therapist-guided internet-delivered cognitive-behavior therapy (iCBT) for adult obsessive-compulsive disorder, using a recently developed digital platform.

Detailed Description

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Although cognitive-behavior therapy (CBT) is a well-established first-line treatment for many mental disorders, very few patients receive it due to the shortage of trained professionals, the costs of face-to-face therapy, and geographic barriers. Therapist-guided internet-delivered CBT (iCBT) is a potential solution to this problem but is not generally available in our context.

The investigators plan to:

1. Develop a digital platform for the treatment of mental disorders using therapist-guided iCBT;
2. Assess the feasibility, acceptability, and potential effects of therapist-guided iCBT for adult obsessive-compulsive disorder (OCD) using the platform developed in Objective 1.

Conditions

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Obsessive-Compulsive Disorder (OCD)

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Single-Group Assignment
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Internet-delivered Cognitive Behavioral Therapy (iCBT)

Group Type EXPERIMENTAL

icbt

Intervention Type BEHAVIORAL

12-Week Therapist-Based iCBT for OCD (Adapted Version of OCD Net: https://therapistguide.webcbt.se/index.html)

Interventions

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icbt

12-Week Therapist-Based iCBT for OCD (Adapted Version of OCD Net: https://therapistguide.webcbt.se/index.html)

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Age between 18 and 75
* Internet access
* Principal diagnosis of OCD, based on DSM-5
* Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) Total Severity Score \> 16
* Ability to communicate in Spanish
* For participants taking psychotropic medication for OCD: at least eight weeks on stable medication and willingness to stay on the same medication/doses for the 12 weeks of the study

Exclusion Criteria

* Estimated IQ \< 70, as per the Vocabulary subtest of the Wechsler Adults Intelligence Scale for Children (WISC)
* Eight or more previous sessions of CBT for OCD with an experienced therapist during the last 12 months
* Ongoing psychological treatment for OCD
* Diagnosis of organic brain disorder, intellectual disability, autism spectrum disorder, psychosis, bipolar disorder, low-weight anorexia nervosa, or alcohol/substance dependence
* Immediate risk to self or others (e.g., suicidality)
* Inability to communicate in Spanish
* Low motivation to participate (i.e., the patient does not believe the therapy will be helpful at all)
* Insufficient time to work on the treatment (about 30 minutes per day)
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospital Clinic of Barcelona

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Joaquim Radua, MD

Role: PRINCIPAL_INVESTIGATOR

Instituto de Investigaciones Biomédicas August Pi i Sunyer (IDIBAPS)

Central Contacts

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Miquel A Fullana, PhD

Role: CONTACT

34+637908990

Maria Sagué, MD

Role: CONTACT

34 +932 27 54 00

Other Identifiers

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HCB/2023/0643

Identifier Type: -

Identifier Source: org_study_id

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