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Building Closer Friendships in Social Anxiety Disorder

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Florida State University

Status

Completed

Conditions

Social Anxiety

Treatments

Behavioral: Building Closer Friendships

Study type

Interventional

Funder types

Other

Identifiers

NCT03671577
2018.23774

Details and patient eligibility

About

This study assesses whether a 4-week computerized intervention can be used to decrease fear of intimacy, and loneliness and improve perceived social support in people with Social Anxiety Disorder.

Full description

This study hopes to assess whether a month long computerized intervention aimed at giving people skills to form closer friendships. Participants will be randomized into an active treatment condition or a wait list control. We hypothesize that 1) participants in the treatment condition will have lower fear of intimacy at post treatment than those in the waitlist condition 2) participants in the treatment condition will have lower levels of loneliness than those in the waitlist condition 3) participants in the treatment condition will have higher perceived social support than those in the waitlist condition.

Enrollment

55 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Social Anxiety Disorder Diagnosed by the Mini International Neuropsychiatric Interview
  • Social Phobia Inventory Score >19
  • Stable psychotropic medication for the past month and kept stable for duration of study

Exclusion criteria

  • Currently participating in therapy
  • Current Substance Dependence
  • Bipolar Disorder or psychotic illness
  • Current suicidality (imminent risk)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

55 participants in 2 patient groups

Active Treatment
Experimental group
Description:
four week computerized intervention designed to reduce fear of intimacy
Treatment:
Behavioral: Building Closer Friendships
Wait List Control
No Intervention group
Description:
Participants will continue as usual and will be given the option to receive the active treatment after completion of the study

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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