NCT02818088

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.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
9

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2016

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2016

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

June 27, 2016

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 29, 2016

Completed
3.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2019

Completed
Last Updated

May 6, 2021

Status Verified

May 1, 2021

Enrollment Period

3.8 years

First QC Date

June 27, 2016

Last Update Submit

May 3, 2021

Conditions

Outcome Measures

Primary Outcomes (2)

  • Yale-Brown Obsessive Compulsive Scale (YBOCS)

    Immediately after intervention

  • Cambridge neuropsychological test automated battery (CANTAB)

    Immediately after intervention

Study Arms (1)

Cognitive Training

EXPERIMENTAL

Cognitive Training - n Back.

Behavioral: n-Back (Cognitive Training)

Interventions

Cognitive Training

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stellenbosch University

Cape Town, Western Cape, 7505, South Africa

Location

MeSH Terms

Conditions

Obsessive-Compulsive Disorder

Interventions

Cognitive Training

Condition Hierarchy (Ancestors)

Anxiety DisordersMental Disorders

Intervention Hierarchy (Ancestors)

Neurological RehabilitationRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsHealth ServicesHealth Care Facilities Workforce and Services

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor Christine Lochner

Study Record Dates

First Submitted

June 27, 2016

First Posted

June 29, 2016

Study Start

February 1, 2016

Primary Completion

December 1, 2019

Study Completion

December 1, 2019

Last Updated

May 6, 2021

Record last verified: 2021-05

Data Sharing

IPD Sharing
Will not share

Locations