Study Stopped
The app platform was cancelled and key personnel withdrew from the project
Cognitive Training in Obsessive Compulsive Disorder
CTOCD
Cognitive Training in Patients With Obsessive Compulsive Disorder
1 other identifier
interventional
9
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2016
Longer than P75 for not_applicable
1 active site
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
CompletedFirst Submitted
Initial submission to the registry
June 27, 2016
CompletedFirst Posted
Study publicly available on registry
June 29, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2019
CompletedMay 6, 2021
May 1, 2021
3.8 years
June 27, 2016
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
EXPERIMENTALCognitive Training - n Back.
Interventions
Eligibility Criteria
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
- University of Stellenboschlead
- University of Cape Towncollaborator
Study Sites (1)
Stellenbosch University
Cape Town, Western Cape, 7505, South Africa
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
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