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Efficacy of Cognitive Bias Modification in Residential Treatment for Addiction

C

Center for Addiction and Mental Health (CAMH)

Status

Completed

Conditions

Substance Dependence

Treatments

Behavioral: Cognitive Bias Modification

Study type

Interventional

Funder types

Other

Identifiers

NCT03000699
077/2016

Details and patient eligibility

About

The purpose of this study is to determine whether computer bias modification for interpretation bias (CBM-I) is effective in the reduction of suicidal ideation in substance use disorders.

Full description

Eighty-eight adult inpatients completing residential treatment in the Addictions Services at the Centre for Addiction and Mental Health (CAMH) will be randomized to receive CBM-I daily for one week, adjunct to the residential psychosocial treatment or to an assessment-only control condition. Participants will complete clinical measures consisting of interviews and questionnaires measuring suicidal ideation, hopelessness, depression, negative affect, and interpretation biases before, during and after treatment.

Enrollment

88 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Exhibit moderate suicide risk or greater
  • Be enrolled in the Addictions Services inpatient program
  • Fluent in reading English
  • Capacity to give informed consent

Exclusion criteria

  • A lifetime diagnosis of a psychotic or bipolar disorder
  • Significant neurological disorder or psychical illness likely to interfere with participation
  • Psychotropic medication changes within the past two weeks

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

88 participants in 2 patient groups

Cognitive Bias Modification
Experimental group
Description:
64 training paragraphs, approximately 10-20 seconds each, digitally recorded and presented stereophonically through headphones, delivered over the course of one week.
Treatment:
Behavioral: Cognitive Bias Modification
Assessment-Only Control
No Intervention group
Description:
No training will be provided.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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