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Clinical Trials/NCT02818088
NCT02818088
Terminated
Not Applicable

Cognitive Training in Patients With Obsessive Compulsive Disorder

University of Stellenbosch1 site in 1 country9 target enrollmentFebruary 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obsessive-Compulsive Disorder
Sponsor
University of Stellenbosch
Enrollment
9
Locations
1
Primary Endpoint
Cambridge neuropsychological test automated battery (CANTAB)
Status
Terminated
Last Updated
4 years ago

Overview

Brief Summary

This unique study will allow us to observe the neural correlates associated with working memory in an obsessive compulsive disorder (OCD) paradigm. We believe that developing working memory in participants suffering with OCD will reduce the severity of their symptomology. This will allow a greater understanding into the functioning of these participants which in turn presents with treatment possibilities.

Detailed Description

It is currently unclear whether cognitive training using a working memory task, is effective in reducing obsessive-compulsive symptoms and neuropsychological deficits in patients with OCD. Two groups (OCD and control) will be recruited. Both groups will undergo an intervention consisting of 8 weeks of cognitive training. Working memory, neuropsychological functioning and OCD symptomatology will be assessed pre and post-treatment, in both groups. Furthermore neuroimaging using functional magnetic resonance imaging (fMRI) will be conducted at baseline as well as at the end of the 8 week period in both groups. The scan will serve to show any structural or functional changes in the frontostriatal area involved with working memory. To our knowledge, this is one of the first studies to date to examine whether cognitive training improves symptoms in OCD.

Registry
clinicaltrials.gov
Start Date
February 2016
End Date
December 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christine Lochner

Professor Christine Lochner

University of Stellenbosch

Eligibility Criteria

Inclusion Criteria

  • A primary diagnosis of OCD, with a score \> 16 on the Yale-Brown Obsessive Compulsive Scale (YBOCS) (Goodman et al, 1989b, 1006-1011).
  • Participants must be aged older than 18 and younger than 65 years.
  • Right handed.
  • If taking SSRI's the participant needs to be on a stable dose for at least 2 months.

Exclusion Criteria

  • Significant physical or neurological illnesses. An exception will be made for patients taking SSRI's (and not using any other drugs).
  • Any significant current DSM disorder (in addition to OCD).
  • Past history of significant substance or alcohol abuse.
  • Pregnancy.
  • Any metal pins/ prostheses or cardiac pacemakers.
  • Sufferers of claustrophobia.
  • Head injury

Outcomes

Primary Outcomes

Cambridge neuropsychological test automated battery (CANTAB)

Time Frame: Immediately after intervention

Yale-Brown Obsessive Compulsive Scale (YBOCS)

Time Frame: Immediately after intervention

Study Sites (1)

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