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A computer based training in anxiety

A computer based training in anxiety - A computer based training in anxiety

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29926
Enrollment
40
Registered
2006-09-19
Start date
2006-11-03
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

anxiety fear

Interventions

The training consists of eight internet-based sessions. During training, participants will learn to interpret ambiguous social information positively (or partly positive and partly negative, dependi

Sponsors

Universiteit Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - panic disorder, with or without agoraphobia (PD) - social phobia (SP) - generalised anxiety disorder (GAD) - posttraumatic stress disorder (PTSD) - depression, with a secundair anxiety disorder -need to have internet access at home - Dutch as their first language

Exclusion criteria

Exclusion criteria: -specific phobia -obsessive-compulsive disorder (OCD) -substance-induced anxiety disorder -comorbid psychotic disorder or substance-related disorder

Design outcomes

Primary

MeasureTime frame
1) It is hypothesised that the positive interpretive training is effective in affecting existing tendencies to interpret ambiguous information negatively. After training, the experimental and control group will differ in their interpretation of ambiguous information. As opposed to the control group, the experimental group will give more positive interpretations and less negative interpretations. 2) if hypothesis 1) is confirmed, then the second hypothesis is that mood and general psychological functioning will remain relatively stable in the control group and will improve in the experimental group. More specifically, level of anxiety, depression, and general dysfunctioning will decrease and positive mood will increase in the experimental group compared to the control group.

Secondary

MeasureTime frame
n.v.t.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)