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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02356718
Other study ID # 0422014
Secondary ID
Status Completed
Phase N/A
First received February 2, 2015
Last updated July 25, 2016
Start date January 2015
Est. completion date July 2016

Study information

Verified date July 2016
Source Centre for Addiction and Mental Health
Contact n/a
Is FDA regulated No
Health authority Canada: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study examines whether computer tasks can improve memory and other cognitive functions among patients receiving inpatient treatment for substance use disorders.


Description:

Participants will complete cognitive training sessions on a regular basis during inpatient treatment. Alternate versions of the computer tasks will be compared in a randomized design. Primary and secondary outcomes will consist of changes in cognitive performance before and after the training period.


Recruitment information / eligibility

Status Completed
Enrollment 111
Est. completion date July 2016
Est. primary completion date July 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Participants must be patients registered for inpatient treatment at the Centre for Addiction and Mental Health

- Age 18-60

- Fluency in English

- Able to attend scheduled training sessions

- Comfortable using a computer and mouse

Exclusion Criteria:

- Severe cognitive impairment

- Current or past psychosis or diagnosis of schizophrenia

- Photosensitive epilepsy or history of seizures triggered by light

- Legal mandate to attend treatment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Behavioral:
Cognitive training activities
Training activities consist of computer tasks designed to improve memory and cognition. The intervention consists of 45-minute training sessions delivered regularly during inpatient treatment.
Inpatient psychosocial therapy
Group psychosocial therapy delivered in an inpatient setting.

Locations

Country Name City State
Canada Centre for Addiction and Mental Health Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
Centre for Addiction and Mental Health

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Auditory memory capacity - WAIS Digit Span score WAIS Digit Span score Baseline, 3 weeks No
Secondary Auditory memory capacity - WAIS Letter-number sequencing score WAIS Letter-number sequencing score Baseline to 3 weeks No
Secondary Visual memory capacity - WMS Spatial span score WMS Spatial span score Baseline to 3 weeks No
Secondary Visual memory capacity - WMS Symbol span score WMS Symbol span score Baseline to 3 weeks No
Secondary Training progress score - Cognitive progress indicator score Cognitive progress indicator score Baseline to 4 weeks No
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