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ITreatOCD: Predicting the Efficacy of Internet-based Cognitive Behavioral Therapy in Obsessive-compulsive Disorder

Not Applicable
Recruiting
Conditions
Obsessive-Compulsive Disorder
Interventions
Behavioral: ICBT
Registration Number
NCT05906069
Lead Sponsor
Pedro Morgado
Brief Summary

In the current study, the investigators will characterize obsessive-compulsive disorder (OCD) patients and healthy controls with a comprehensive clinical and neuroimaging assessment, focusing on the basic psychological processes related and on the neurobiological underpinnings of emotion regulation (ER). After a baseline assessment, the investigators will implement an internet-based cognitive behavioral therapy (iCBT) protocol and assess its efficacy on the modulation of ER and OCD severity. Specifically, the investigators will (1) examine to what extent the iCBT intervention modulates ER and the associated neurobiological mechanisms and (2) identify candidate biomarkers of successful treatment response.

Detailed Description

Sixty patients and sixty controls will be recruited at Hospital de Braga, Braga, Portugal (sample size estimated based on a previous systematic review). A power analysis indicated that a sample of 24 individuals per group is adequate to detect an effect size of d=.89, with a Type I error of .05 and a statistical power of .85. A final sample of 30 individuals was defined to account for a 20% dropout rate during the intervention.

All participants will be assessed with a comprehensive psychological and clinical characterization. Following the baseline assessment, OCD patients will be randomly allocated to the intervention (iCBT intervention) or the control group (waiting list). The iCBT intervention will consist of a structured program comprising 10 modules with text and video content, as well as 3 videoconferencing psychotherapy sessions. After the intervention/waiting list, patients will be re-assessed with the clinical and psychological assessment.

In order to characterize the patterns of brain activation in OCD patients during an emotion regulation task in comparison to healthy controls and to identify potential neurobiological markers of symptoms' improvement, a multimodal neuroimaging assessment will also be performed. The task encompasses the presentation of pictures (fearful, neutral and OCD-related stimuli) under two conditions: the instruction to view the pictures naturally ('observe'); or to apply cognitive reappraisal techniques to decrease any negative affective state caused by the stimuli ('regulate'). Fear and OCD-related pictures are presented during both conditions; neutral pictures only during 'observe'. After each stimulus, the level of distress will be assessed by a self-report rating scale.

In the baseline assessment, brain activation patterns (with whole-brain and region of interest approaches) will be compared between OCD and healthy controls in both task conditions. After intervention, emotion regulation ability and the underlying neurobiological mechanisms will be compared between the 'intervention' and 'waiting list' groups.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Primary diagnosis of current OCD according to the fifth Diagnostic and Statistical Manual of Mental Disorders
  • YBOCS score ≥ 16
  • Psychotropic medication, if stable for at least 2 months prior to inclusion and if the dosage is maintained thoughout the study
  • Have the resources to access the online intervention (internet access; computer or tablet)
Exclusion Criteria
  • MRI contraindications
  • Prior medical history of neurological disorders or traumatic brain injury
  • Having performed CBT treatment for OCD in the last 2 years
  • Undergoing any psychological treatment
  • Suicidal ideation
  • Current alcohol or drug abuse

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
iCBT interventionICBTParticipants will enroll in an internet-based cognitive behavioral program during 14 weeks. The program comprises 10 modules and three videoconferencing psychotherapy sessions.
Primary Outcome Measures
NameTimeMethod
Change in the Yale-Brown Obsessive Compulsive Scale (Y-BOCS)immediately before and immediately after intervention/waitlist

Psychometric scale to assess obsessive-compulsive symptoms

Secondary Outcome Measures
NameTimeMethod
Obsessive-Compulsive Inventory- Revisedbaseline; 4 weeks after beginning intervention/waitlist; 8 weeks after beginning; 12 weeks after beginning intervention/waitlist and immediately after intervention/waitlist

Psychometric scale to assess obsessive-compulsive symptoms

Hamilton Anxiety Scaleimmediately before and immediately after intervention/waitlist

Psychometric scale to assess anxiety symptoms

Hamilton Depression Scaleimmediately before and immediately after intervention/waitlist

Psychometric scale to assess depression symptoms

Perceived Stress Scaleimmediately before and immediately after intervention/waitlist

Psychometric scale to assess stress symptoms

Positive and Negative Affect Scheduleimmediately before and immediately after intervention/waitlist

Psychometric scale to assess affect

Depression Anxiety Stress scalebaseline; every week during intervention/wait list (up to 14 weeks) and immediately after intervention/waitlist

Psychometric scale to assess symptoms of anxiety, depression and stress

Treatment Acceptability/Adherence Scaleimmediately after intervention

Psychometric scale to assess treatment adherence

University of Rhode Island Change Assessment Scalebaseline

Psychometric scale to assess motivation to change

Emotion Regulation Questionnaireimmediately before and immediately after intervention/waitlist

Psychometric scale to assess cognitive regulation and emotional suppression capabilities

Difficulties in Emotion Regulation Scaleimmediately before and immediately after intervention/waitlist

Psychometric scale to assess emotion deregulation

NEO Five-Factor Inventorybaseline

Psychometric scale to assess personality traits

Trial Locations

Locations (1)

Life and Health Sciences Research Institute, School of Medicine, University of Minho

🇵🇹

Braga, Gualtar, Portugal

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