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NCT Number: NCT05906069

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

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

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

Braga, Gualtar, 4710-057, Portugal

Location status: Recruiting

Location contact

Mafalda Sousa, M. Sc.

CONTACT

[email protected]

Pedro Morgado, M.D, Ph.D.

CONTACT

[email protected]

00351 253 604 931

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

ICBT

Behavioral

The intervention will consist in a structured internet-based intervention with 10 modules that will combine cognitive-behavioral techniques to improve obsessive-compulsive symptoms as well as the emotion regulation ability.

Primary outcomes

  1. Change in the Yale-Brown Obsessive Compulsive Scale (Y-BOCS)

    Time frame: immediately before and immediately after intervention/waitlist

    Psychometric scale to assess obsessive-compulsive symptoms

Secondary outcomes

  1. Obsessive-Compulsive Inventory- Revised

    Time frame: baseline; 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

  2. Hamilton Anxiety Scale

    Time frame: immediately before and immediately after intervention/waitlist

    Psychometric scale to assess anxiety symptoms

  3. Hamilton Depression Scale

    Time frame: immediately before and immediately after intervention/waitlist

    Psychometric scale to assess depression symptoms

  4. Perceived Stress Scale

    Time frame: immediately before and immediately after intervention/waitlist

    Psychometric scale to assess stress symptoms

  5. Emotion Regulation Questionnaire

    Time frame: immediately before and immediately after intervention/waitlist

    Psychometric scale to assess cognitive regulation and emotional suppression capabilities

  6. Difficulties in Emotion Regulation Scale

    Time frame: immediately before and immediately after intervention/waitlist

    Psychometric scale to assess emotion deregulation

  7. Positive and Negative Affect Schedule

    Time frame: immediately before and immediately after intervention/waitlist

    Psychometric scale to assess affect

  8. Depression Anxiety Stress scale

    Time frame: baseline; 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

  9. NEO Five-Factor Inventory

    Time frame: baseline

    Psychometric scale to assess personality traits

  10. Treatment Acceptability/Adherence Scale

    Time frame: immediately after intervention

    Psychometric scale to assess treatment adherence

  11. University of Rhode Island Change Assessment Scale

    Time frame: baseline

    Psychometric scale to assess motivation to change

Study contacts

Contact information is provided by the study sponsor or research team.

Mafalda Sousa, M., Sc.

CONTACT

[email protected]

Pedro Morgado, M.D, Ph.D.

CONTACT

[email protected]

+351 253 604 931

Sponsors and collaborators

Lead sponsor

Pedro Morgado

Other

Collaborators

  • Associação Centro de Medicina P5 (ACMP5)
  • Clinical Academic Center (2CA)
  • Hospital de Braga
  • ICVS - Life and Health Sciences Research Institute

Registry information

Official study title

ITreatOCD: Predicting the Efficacy of Internet-based Cognitive Behavioral Therapy from Changes in the Neurobiological Correlates of Emotion Regulation in Obsessive-compulsive Disorder

Acronym: iTREATOCD

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Jun 15, 2023
Registry last updated
Jan 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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