We updated the design of this site on December 18, 2017. Learn more.
ClinicalTrials.gov
ClinicalTrials.gov Menu

Online Program for Social Anxiety

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT02792127
Recruitment Status : Completed
First Posted : June 7, 2016
Last Update Posted : December 29, 2017
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
The purpose of this study is to investigate the efficacy of an online program in reducing symptoms of social anxiety, unhelpful thoughts, avoidance behaviours, fear of negative evaluations and improving quality of life in students with above-average social anxiety.

Condition or disease Intervention/treatment
Social Anxiety Behavioral: Online Program for Social Anxiety

Detailed Description:

While there are many benefits to online programs in treating a variety of health issues (i.e., implementation in remote areas, cost-effectiveness, etc.), the primary challenge for online formats is to imitate real-life interactions while promoting a reduction in symptoms. This will be attempted in a six-month online program for social anxiety.

The present study will assess the efficacy of a six-month online program through measures of social anxiety, fear of negative evaluations, unhelpful thoughts, avoidance behaviours and quality of life. This information will be collected from students at baseline and upon completion of the online program.


Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 101 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: Online Cognitive Behavioural Therapy Program for Social Anxiety
Study Start Date : July 2016
Primary Completion Date : December 2017
Study Completion Date : December 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Anxiety
U.S. FDA Resources

Arms and Interventions

Arm Intervention/treatment
Experimental: Experimental
These participants will be given access to a six-month online program for social anxiety.
Behavioral: Online Program for Social Anxiety
This program will be completed from participants' homes using their own computers. This online format is based on a Cognitive Behaviour Therapy framework (CBT) and involves seven modules that ask participants to engage in a variety of thinking exercises and activities.
No Intervention: Wait List Control
These participants will not be given an intervention until after they have completed the study.


Outcome Measures

Primary Outcome Measures :
  1. Social Anxiety [ Time Frame: six months ]
    A self-report measure that assesses symptoms of distress experienced when socializing with others.


Eligibility Criteria

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Registered UBC student
  • Achieve an above-average score on a validated screening tool for social anxiety

Exclusion Criteria:

  • Not a registered UBC student
  • Clinical diagnosis of a mental illness
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02792127


Sponsors and Collaborators
University of British Columbia
Investigators
Principal Investigator: Frances Chen, PhD University of British Columbia
More Information

Publications:
Helgadottir FD, Ross MG, Onslow M, Packman A, O'Brian, S. Online CBT II: A phase I trial of a standalone, online CBT Treatment Program for Social Anxiety in Stuttering. Behaviour Change 26(4): 254-270. 2009.
Helgadottir FD, Menzies RG, Onslow M, Packman A, O'Brian S. Online CBT I: Bridging the gap between Eliza and modern online CBT treatment packages. Behaviour Change 26(4): 245-253, 2009.

Responsible Party: Frances Chen, Assistant Professor, University of British Columbia
ClinicalTrials.gov Identifier: NCT02792127     History of Changes
Other Study ID Numbers: H16-00319
First Posted: June 7, 2016    Key Record Dates
Last Update Posted: December 29, 2017
Last Verified: December 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Frances Chen, University of British Columbia:
Social Anxiety
Cognitive Behaviour Therapy
Online Program

Additional relevant MeSH terms:
Anxiety Disorders
Mental Disorders