None listed
Conditions
Brief summary
This randomised controlled trial seeks to explore the feasibility of a novel treatment format for social anxiety disorder; online cognitive behavioural therapy delivered in an intensive format across just one week. Outcomes will be compared between the intervention and control groups from pre- to post-treatment, and one-month follow-up.
Interventions
The internet-delivered Cognitive Behavioural Therapy Program comprises 6 lessons completed over 7 days. It includes psychoeducation about anxiety and management of its physical symptoms, graded exposure to overcome avoidance, behavioural experiments to test maladaptive beliefs, thought challenging to address unhelpful thoughts, social skills training and relapse prevention. A new lesson will become available each day (with the exception of Day 6, which is devoted to practicing challenging skills), with participants expected to complete one lesson per day. Each lesson will take approximately 30-40 minutes to read. Participants will have access to summaries of each lesson, homework exercises and extra resources for each lesson. Participants are advised to spend at least 3-4 hours per day (for a 7 days) working through the lesson material, revisiting the content and homework tasks/practicing the skills. Clinician guidance will be provided to participants randomly allocated to the intervention group in the form of email or phone contact from the clinicians (registered clinical psychologist; registered provisional psychologist undertaking postgraduate training). Participants in the intervention group are able to email or phone the clinician at any point during the trial. Participants in the waitlist control group can contact research staff for technical assistance at any point via phone or email. Participants in the intervention group will complete a measure of social anxiety symptoms, depression, and personality traits and functioning before the first lesson (baseline), one week after the program (two weeks post baseline), and at 1-month follow-up (six weeks post baseline). Participants in the control group will complete these same measures at baseline, two weeks post baseline, and six weeks post baseline before being offered the intervention program. Across both groups, if participants' scores deteriorate by 4 or more points, the clinician is automatically alerted and initiates contact with the participant by phone or email. If the participant has an elevated distress or depression score, the clinician is automatically alerted and initiates contact with the participant by phone or email. The mode of contact is dependent on what is clinically indicated in terms of the participant's distress score and/or what the participant may have communicated (in the form of phone or email contact) to the clinician. The mode of contact (email or phone or both) therefore is dependent on the clinician's clinical judgement of the situation in hand. Strategies used to improve adherence to intervention protocols and procedures for monitoring adherence include: automated email reminders, monitoring the downloading of homework, and collection of data on how long participants spent reading lessons and practicing skills.
Sponsors
Study design
Eligibility
Inclusion criteria
- Self-identified as experiencing social anxiety. - Meet DSM-5 criteria for social anxiety as assessed by abbreviated diagnostic interview for DSM-5. - At least 18 years of age. - Live in Australia. - Fluent in English. - Have access to a phone and a computer that is connected to the internet. - If taking medication for mental-health, must be on a stable dose of medication (past 8 weeks prior to intake). - Prepared to provide name, phone number, and address. - Willing to provide informed consent.
Exclusion criteria
- Does not meet criteria for social anxiety disorder. - Self-reported diagnosis of schizophrenia, bipolar disorder, or current psychotic symptoms. - Current suicidal ideation (deemed as responding 3 to the PHQ-9 question 9 item that assesses the frequency of suicidal ideation - Severe or very severe depression (PHQ-9 scores of 24 and above) - Commencement of a new mental health medication or change in dose of existing mental health medication in the two months prior to intake. - Currently participating in Cognitive Behavioural Therapy. - Do not complete the online screening questionnaire or unwilling to provide demographic details.