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Disgust Reduction Through Evaluative Conditioning (DREC) and tDCS in Contamination-Based OCD

F

Ferdowsi University of Mashhad

Status

Enrolling

Conditions

Obsessive-Compulsive Disorder

Treatments

Other: Active tDCS
Other: Sham tDCS
Other: Active EC training
Other: Sham EC training

Study type

Interventional

Funder types

Other

Identifiers

NCT05907369
3/56765
100/18979 (Other Identifier)

Details and patient eligibility

About

Obsessive-compulsive disorder (OCD) is a debilitating health condition that is known by intrusive and unwanted thoughts and repetitive behavioral or mental acts. 2-3% of the population suffers from OCD in their lifetime. The most common OCD subtype is contamination. The Serotonin-selective reuptake inhibitors (SSRIs) and cognitive-behavioral therapy (CBT) based on exposure and response prevention (ERP) technique are the first-line treatments for OCD. The challenge is that nearly half do not respond to the first-line treatments or have residual symptoms after completion of treatments. However, the prevalence of the disorder, diversity of symptoms, inadequate response rate, and necessity of having long-lasting treatment effects make the treatments of OCD more challenging.

It seems that abnormal, more intense disgust experience has a prominent role in developing and maintaining OCD symptoms, particularly the contamination subtype. Evaluative conditioning (EC), defined as transferring the value of the US to the CS through pairing them, is the most common way of establishing disgust responses. The present study aims to develop an emotion-based intervention technique using EC targeting disgust emotion in contamination-based OCD (C-OCD). The hypothesis is that EC training may modify disgust experiences. Disgust may be the culprit, at least in part, of cognitive deficiencies in OCD. The other hypothesis is whether disgust reduction-focused EC may improve cognitive function, such as attention bias and inhibitory control.

The orbitofrontal cortex (OFC) is one of the brain areas engaged in disgust processing and is mostly hyperactive in OCD patients. Cathodal transcranial direct current stimulation (tDCS) over OFC is one of the helpful neuromodulation methods in treating OCD. We aim to see if this method may help to regulate disgust experiences in combination with EC. The participants may be referred by psychiatrists or psychotherapists or be self-referred due to online advertisements or paper flyers. They will be randomly assigned to one of for arms of the study for sham or active EC training along with sham or active tDCS, to which they are blind. The novelty of the present study is the application of EC training in the clinical OCD population in combination with a neuromodulation method.

Full description

Disgust as a primary emotion has evolved to protect our lives by driving dirt and disease avoidance behaviors and motivating for cleaning and hygienic behaviors. In recent years, many studies have focused on the role of disgust in psychiatric disorders such as anxiety disorders, eating disorders, body dysmorphic disorders, and phobias. Nowadays, we have robust evidence of the correlation between disgust and the etiology and treatment of OCD symptoms, particularly the contamination subtype. The principal explanation for the insufficient treatment effect of ERP is that disgust is resistant to extinction.

Since evaluative conditioning is one of the main sources of disgust feeling, the same process may effectively reduce disgust. The present trial will try to pair contamination-related pictures that are disgust-eliciting with positive, pleasant pictures in order to modify their disgust valence. We also will administer this EC training plus to OFC cathodal tDCS to see if the EC effect becomes more significant than EC alone.

Enrollment

55 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The Diagnostic criteria of OCD in the Diagnostic and Statistical Manual of Mental Disorders 5th edition (DSM-5-TR) with the symptoms of contamination subtype
  • Able to read, write and do computerized tasks
  • Stable medication for at least the last three months
  • Filling out the written consent

Exclusion criteria

  • Severe physical illness
  • Severe other mental disorders
  • Alcohol and drug dependence
  • A history of epilepsy or seizure
  • Have metal or electronic implants in the head or use a cardiac pacemaker
  • History of head trauma or neurological disorders
  • Women who are pregnant or may be pregnant
  • Unable to complete questionnaires, computerized tasks, or informed consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

55 participants in 4 patient groups

aEC/ stDCS
Experimental group
Description:
Participants in this group receive active EC training but sham tDCS.
Treatment:
Other: Active EC training
Other: Sham tDCS
sEC/atDCS
Active Comparator group
Description:
Participants in this group receive active tDCS training but sham EC training.
Treatment:
Other: Active tDCS
Other: Sham EC training
aEC/atDCS
Experimental group
Description:
Participants in this group receive both active EC training and active tDCS.
Treatment:
Other: Active tDCS
Other: Active EC training
sEC/stDCS
Sham Comparator group
Description:
Participants in this group receive the sham EC training and also sham tDCS.
Treatment:
Other: Sham tDCS
Other: Sham EC training

Trial contacts and locations

1

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Central trial contact

Faezeh Raeisalmohaddesin, MsC; Ali Moghimi, PhD

Data sourced from clinicaltrials.gov

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