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Webbased prevention of social anxiety in adolescents: a pilot study

Webbased prevention of social anxiety in adolescents: a pilot study - Webbased prevention of social anxiety in adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON34064
Enrollment
50
Registered
2010-10-11
Start date
2010-11-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

extreme shyness social anxiety social phobia

Interventions

The intervention is based on the book *Fobieën* (Phobias) by drs. de Neef and prof. Cuijpers (co-applicant of this study). The main component of this course is the evidence-based aspect of cognitive
the exposure. People will need to expose themselves to exactly that what they are anxious about and normally avoid. The course consists of five weekly modules. The participant will be required to d

Sponsors

Vrije Universiteit
Lead Sponsor

Eligibility

Age
12 Years to 17 Years

Inclusion criteria

Inclusion criteria: 1) between 13 and 18 years old ; (2) a score of 1 standard deviation above the population mean on the *Behavioral Inhibition Scale* (BIS); (3) positive answer on the question: 'as long as I remember, I have always been shy' ; and (4) a score above the 75th percentie of the *Social Anxiety Scale for Adolescents* (SAS-A)

Exclusion criteria

Exclusion criteria: Score above the 90th percentile of the 'Social Anxiety Scale for Adolescents* (SAS-A) and receiving treatment for social anxiety elsewhere

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is the feasibility of this intervention. This will be determined by, for example, how many adolescents show interest in the course and eventually sign up for it. The reasons for drop-out, and predictors for finishing the course will be registered. The level of client satisfaction about the course and the coaching will also give an indication of the feasibility and acceptability of the prevention program. Another primary outcome measure will be the effect of the prevention program, measured by the change in social anxiety symptoms on the SAS-A.

Secondary

MeasureTime frame
Secondary outcomes include: depressive symptoms (CES-D), general anxiety symptoms (HADS-A), quality of life (Euroqol) and working alliance (WAI) and client satisfaction.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)