Internet-based guided self-help for social anxiety disorder administered through a mobile app
- Conditions
- Social anxiety disorderMental and Behavioural Disorders
- Registration Number
- ISRCTN10627379
- Lead Sponsor
- Swiss National Science Foundation
- Brief Summary
2018 results in: https://www.ncbi.nlm.nih.gov/pubmed/29781648
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 150
1. Male and female at least 18 years of age
2. Provided written consent
3. Sufficient German language skills
4. Access to computer with internet connection
5. Exceeding pre-defined cut-off scores in one of the social anxiety measures
6. Meeting the diagnostic criteria for SAD according to the diagnostic telephone interview
7. Agreeing to undergo no other psychological treatment for the duration of the study
1. Active suicidal plans (according to the suicide item of the Beck Depression Inventory (BDI) or the diagnostic telephone interview)
2. History of psychotic or bipolar disorders
3. Prescribed medication for anxiety or depression only if the dosage has been changed during the last month prior to the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Symptoms of SAD (Social Phobia Scale [SPS], assessed using Social Interaction Anxiety Scale [SIAS], and Liebowitz Social Anxiety Scale-Self-Report [LSAS-SR]), pre, post (12 weeks), follow-up (6 months)<br>2. Diagnostic status (Structured Clinical Interview for DSM-IV Axis I Disorders [SCID-I]): pre, post (12 weeks), follow-up (6 months)
- Secondary Outcome Measures
Name Time Method 1. Depression, assessed using the Beck Depression Inventory [BDI-II]: pre, post (12 weeks), follow-up (6 months)<br>2. General symptomatology, assessed using the Brief Symptom Inventory [BSI]: pre, post (12 weeks), follow-up (6 months)<br>3. Interpersonal problems, assessed using the Inventory of Interpersonal Problems (IIP-64): pre, post (12 weeks), follow-up (6 months)<br>4. Quality of life, assessed using the SF-12 Health Survey: pre, post (12 weeks), follow-up (6 months)<br>5. Client Satisfaction, assessed using the ZUF-8 general satisfaction questionnaire: post (12 weeks)<br>6. Several process measures:<br>6.1. Change in SAD symptoms: week 2, 4, 6, 8, 10<br>6.2. Individual condition, assessed using the Working Alliance Inventory-Short Revised (WAI-SR): week 2, 4, 6, 8, 10<br>6.3. Treatment expectancy, assessed using the Credibility/Expectancy Questionnaire (CEQ): week 2