Cognitive Training in Obsessive Compulsive Disorder

Not Applicable

Terminated

• Conditions: Obsessive-Compulsive Disorder
• Interventions: Behavioral: n-Back (Cognitive Training)

• Registration Number: NCT02818088
• Lead Sponsor: University of Stellenbosch

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.

Study Timeline

• Study Start: 2016-02
• Study First Submitted: 2016-06-27
• Study First Submitted QC: 2016-06-27
• Study First Posted: 2016-06-29
• Primary Completion: 2019-12
• Study Completion: 2019-12
• Status Verified: 2021-05
• Last Update Submitted: 2021-05-03
• Last Update Posted: 2021-05-06

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 9

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Cognitive Training	n-Back (Cognitive Training)	Cognitive Training - n Back.

Primary Outcome Measures

Name	Time	Method
Cambridge neuropsychological test automated battery (CANTAB)	Immediately after intervention
Yale-Brown Obsessive Compulsive Scale (YBOCS)	Immediately after intervention

Trial Locations

Locations (1)

Stellenbosch University; 🇿🇦 Cape Town, Western Cape, South Africa