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Treatment of social phobia using virtual reality

Virtual reality exposure in social phobia patients: a controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15547690
Enrollment
82
Registered
2015-07-11
Start date
2015-08-03
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Social phobia (SP) Mental and Behavioural Disorders

Interventions

82 patients with social phobia diagnosis will be randomly distributed into two treatment groups: virtual exhibition or live exposure. Therapists with expertise in cognitive behavioral therapy will be

Sponsors

Anxiety Program at the Institute of Psychiatry Faculty of Medicine University of São Paulo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients: 1. Treated at the Psychotherapy Service and Anxiety Program (AMBAN) 2. Aged 18 - 65 3. Can read and write 4. Diagnosised with FS , according to the DSM -5

Exclusion criteria

Exclusion criteria: Patients: 1. With severe major depression 2. At risk for suicide, substance abuse or dependence psychotic disorders 3. Who are in psychotherapy

Design outcomes

Primary

MeasureTime frame
Efficacy will be assessed by: 1. Down 25% to 50% in the LSAS scores will be considered partial response, and above 50% remission 2. Clinical Global Impression presenting scores 0 or 1 on the subscales of severity and improves 3. Sheehan Disability Scale presenting scores 0-3 in each of the three subscales (Work, Social Life and Family Life)

Secondary

MeasureTime frame
Secondary measures: 1. Accession shall be assessed by the number of dropouts 2. The habituation, decreased anxiety during the exposure procedure is assessed by the duration in minutes for the sessions that subjective discomfort units fall from 25% to 50% 3. The duration of therapy will be evaluated by the number of sessions required for habituation to occur 4. Depressive symptoms will be assessed by the Beck Depression Inventory for (BDI) considering improves a lower score than 10 5. Improved quality of life will be assessed by Scale Social-EAS Adequacy (Weissman and Bothwell, 1976) 6. Customer satisfaction with treatment will be evaluated by CSQ-8 7. The therapeutic alliance (bond) will be evaluated by WAI

Countries

Brazil

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026