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Clinical Trials/ACTRN12622000361707
ACTRN12622000361707
Recruiting
未知

A randomised controlled trial exploring the efficacy of an intensive 7-day online CBT program for reducing symptoms of social anxiety disorder compared to waitlist control.

SW Sydney0 sites50 target enrollmentMarch 1, 2022
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ConditionsSocial Anxiety DisorderMental Health - Anxiety

Overview

Phase
未知
Intervention
Not specified
Conditions
Social Anxiety Disorder
Sponsor
SW Sydney
Enrollment
50
Status
Recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 1, 2022
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
SW Sydney

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

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