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N/A N=76 Randomized Treatment

Internet Treatment for Social Phobia in Romania

Phobia, Social

Enrolled (actual)
76
Serious AEs
Results posted
Aug 2014
Primary outcome: Primary: Leibowitz Social Anxiety Scale - Self Report (LSAS-SR) — 78.60; 78.47; 73.69; 43.98 units on a scale — p=<0.01

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
iSOFIE (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Babes-Bolyai University
Primary completion
Mar 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Leibowitz Social Anxiety Scale - Self Report (LSAS-SR)
78.60; 78.47; 73.69; 43.98; NA; 35.77 <0.01 sig
PRIMARY
Social Phobia Inventory (SPIN)
45.50; 45.15; 43.22; 27.95; NA; 19.74 <0.01 sig
SECONDARY
Beck Depression Inventory-II (BDI-II)
15.39; 15.15; 12.77; 7.25; NA; 6.44 <0.01 sig
SECONDARY
Attitude and Belief Scale-II (ABS-II)
124.60; 120.94; 102.51; 76.62; NA; 57.96 <0.01 sig
SECONDARY
Anxiety Sensitivity Index (ASI)
29.00; 29.28; 26.17; 18.38; NA; 13.40 <0.01 sig

Summary

The main aim of this study is to investigate the effectiveness of an Internet-delivered intervention for social phobia by comparing it to a waitlist control group. The second aim of the study is to track the potential changes in participants' thinking patterns. Because this is among the first guided Internet-delivered interventions conducted in Romania, the treatment credibility will also be investigated. Finally, the predictive power of anxiety sensitivity for both SAD symptoms and the treatment effectiveness will be investigated.

Eligibility Criteria

Inclusion Criteria

  • over 18 years
  • social anxiety disorder is the primary diagnostic (according to the DSM-IV)
  • access to an Internet connected computer
  • be fluent in Romanian language

Exclusion Criteria

  • suicidal ideation
  • ongoing psychological treatment for social anxiety disorder
  • recent change in psychiatric medication (i.e., during the last 6 weeks)
  • psychoses or borderline personality disorder
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01557894). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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