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Cognitive Bias Modification (CBM) and Obsessive Compulsive Beliefs

A randomised controlled trial comparing Internet based cognitive bias modification (Active version) for obsessive compulsive disorder vs. Internet based cognitive bias modification (Control version) on negative interpretation bias.

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12613001130752
Enrollment
14
Registered
2013-10-10
Start date
2013-10-25
Completion date
2014-09-22
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This RCT will evaluate the acceptability and efficacy of a multi-day online CBM program targeting obsessive compulsive beliefs by comparing an active CBM intervention with a control comparator.

Interventions

Internet-based cognitive bias modification intervention with 4 sessions (1 x 20 minute session/day) of written scenarios delivered over 1 week. Each CBM session consists of delivery of 41 initially ambiguous scenarios that 100% of the time terminate with a positive resolution. Adherence to the daily CBM sessions will be automatically tracked by the computer program. Standardised email reminders will be sent to a participant if more than 2 days lapse between logins. Each of the 164 training s

Internet-based cognitive bias modification intervention with 4 sessions (1 x 20 minute session/day) of written scenarios delivered over 1 week. Each CBM session consists of delivery of 41 initially ambiguous scenarios that 100% of the time terminate with a positive resolution. Adherence to the daily CBM sessions will be automatically tracked by the computer program. Standardised email reminders will be sent to a participant if more than 2 days lapse between logins. Each of the 164 training scenarios is followed by a comprehension question to ascertain compliance with the training instructions.

Sponsors

St Vincent's Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Meet Lifetime diagnostic criteria for Obsessive Compulsive Disorder (DSM-IV and DSM 5 criteria will be assessed). Internet access; Australian resident; Fluent in written and spoken English.

Exclusion criteria

Presence of severe depression and/or suicidal ideation; lifetime psychotic symptoms or bipolar disorder; current substance abuse; current or planned psychological treatment during study duration; change in medication during last 1 month or intended change during study duration, use of Benzodiazepines; not fluent in written and spoken English.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 20, 2026