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Trial registered on ANZCTR
Registration number
ACTRN12607000256471
Ethics application status
Approved
Date submitted
7/03/2007
Date registered
14/05/2007
Date last updated
14/05/2007
Type of registration
Retrospectively registered
Titles & IDs
Public title
The use of Oxytocin in combination with exposure therapy to treat social anxiety symptoms.
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Scientific title
A randomised controlled trial to evaluate the effect of Oxytocin (OT; 24 IU) in combination with exposure therapy for the treatment of social phobia to improve the severity of social phobia symptoms.
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Secondary ID [1]
364
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Therapeutic Goods Association Clinical Trial Notification (TGA CTN): YGA CTN - 2006/314
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Social Phobia
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Condition category
Condition code
Mental Health
1881
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0
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Other mental health disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants with social phobia are given group exposure based therapy over 5 weekly treatment sessions in combination with a Nasal Spray dose of Oxytocin (OT; 24 IU). Exposure therapy consists of 3 to 10 minute speech tasks in front of a group where a decrease in anxiety within this situation is observed.
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Intervention code [1]
1594
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Treatment: Drugs
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Comparator / control treatment
Placebo matched Nasal spray taken only before therapy sessions once a week for four weeks.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Severity of Social Phobia Symptoms
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Assessment method [1]
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Timepoint [1]
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Assessed one month post-treatment
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Secondary outcome [1]
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General functioning
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Assessment method [1]
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Timepoint [1]
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Assessed at one-month follow-up.
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Eligibility
Key inclusion criteria
University students over the age of 18.
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Minimum age
18
Years
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Maximum age
Not stated
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Under 18, pregnancy, epilepsy, substance abuse/ dependence, psychotic symptoms, suicidal thoughts. Participants are also instructed not to drink alcohol, caffeine or take any illegal drugs on the day of Oxytocin (OT) administration, and to abstain from fluids and food, except water, two hours before OT administration.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Drug Allocation Concealmet is conducted by numbering all containers
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Random number generation using computer software. There is no stratification
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
All subjects, assessors, therapists, and data entry staff are blind to drug condition
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Phase
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/02/2007
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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University of New South Wales
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Address [1]
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Country [1]
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Australia
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Primary sponsor type
University
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Name
University of New South Wales
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Address
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Country
Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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University of New South Wales
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Ethics committee address [1]
3760
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
3760
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Approval date [1]
3760
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Ethics approval number [1]
3760
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HREC06266
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Summary
Brief summary
This study tests whether Oxytocin improves the effectiveness of exposure therapy for decreasing social anxiety symptoms. We predict that individuals from the community diagnosed with social phobia who receive four exposure therapy sessions in combination with Oxytocin will experience a greater reduction in social anxiety symptoms in comparison to individuals who received the placebo in combination with four exposure therapy sessions. Participants receive, in total, five weekly group therapy sessions, the first is educational and the next four consist of public speaking exposure therapy. One month post intervention participants are assessed for social anxiety symptoms as well as other general health indicators. All subjects, therapists, assessors, and data entry staff are blind to condition.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr. Adam Guastella
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Address
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School of Psychology
University of New South Wales
Kensington, 2052
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Country
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Australia
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Phone
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02 9385 8071
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Fax
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02 9385 3641
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr. Adam Guastella
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Address
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School of Psychology
University of New South Wales
Kensington NSW 2052
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Country
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Australia
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Phone
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02 9385 8071
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Fax
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02 9385 3641
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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