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Trial registered on ANZCTR
Registration number
ACTRN12605000392662
Ethics application status
Approved
Date submitted
5/09/2005
Date registered
14/09/2005
Date last updated
14/09/2005
Type of registration
Retrospectively registered
Titles & IDs
Public title
Comparative Study on Group Therapy for Generalised Anxiety Disorder
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Scientific title
A randomised study to compare the effectiveness of three forms of group therapy for the treatment of generalised anxiety disorder. Outcomes measured are changes in symptoms and psychological processes commonly associated with GAD.
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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:
Generalised Anxiety Disorder
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Condition category
Condition code
Mental Health
576
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Anxiety
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants are randomly assigned to one of three forms of group psychotherapy: cognitive behaviour therapy, emotion focused therapy, or psychodynamic therapy. Each group therapy has a dosage of a 2 hour session each week for 9 weeks.
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Intervention code [1]
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None
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
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Self report measure: State-Trait Anxiety Inventory Depression Anxiety Stress Scale (DASS)
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Assessment method [1]
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Timepoint [1]
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Measured at pre-therapy, post-therapy and 6 month follow-up
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Primary outcome [2]
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Self report measure: Penn State Worry Scale
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Assessment method [2]
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Timepoint [2]
663
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Measured at pre-therapy, post-therapy and 6 month follow-up
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Primary outcome [3]
664
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Self report measure:Anxiety Sensitivity Index
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Assessment method [3]
664
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Timepoint [3]
664
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Measured at pre-therapy, post-therapy and 6 month follow-up
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Primary outcome [4]
665
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Self report measure:Anxious Thoughts Questionnaire
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Assessment method [4]
665
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Timepoint [4]
665
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Measured at pre-therapy, post-therapy and 6 month follow-up
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Primary outcome [5]
666
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Self report measure: Meta-Cognitions Questionnaire
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Assessment method [5]
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Timepoint [5]
666
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Measured at pre-therapy, post-therapy and 6 month follow-up
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Primary outcome [6]
667
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Self report measure: Toronto Alexithymia Scale (TAS-20)
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Assessment method [6]
667
0
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Timepoint [6]
667
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Measured at pre-therapy, post-therapy and 6 month follow-up
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Primary outcome [7]
668
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Self report measure: Interpersonal sensitivity index
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Assessment method [7]
668
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Timepoint [7]
668
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Measured at pre-therapy, post-therapy and 6 month follow-up
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Primary outcome [8]
669
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Self report measure: Working Alliance
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Assessment method [8]
669
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Timepoint [8]
669
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Measured at pre-therapy, post-therapy and 6 month follow-up
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Secondary outcome [1]
1376
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Heart rate variabilty
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Assessment method [1]
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Timepoint [1]
1376
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Measured at pre-therapy and post-therapy.
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Eligibility
Key inclusion criteria
Criteria DSM IV diagnosis of Generalised Anxiety Disorder.
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Minimum age
18
Years
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Maximum age
65
Years
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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
Poor English language abilitiesCognitive deficits (intellectual disability, dementia, delirium, significant head injury)Psychotic illnessDisclosure of risk of harm to self or others.
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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)
Sealed envelopes.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
sequence generated by roll of dice
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
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Type of endpoint/s
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
3/01/2005
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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
60
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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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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QUT Internal Grant
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Address [1]
626
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Country [1]
626
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Australia
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Primary sponsor type
Individual
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Name
Esben Strodl
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Address
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Country
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Secondary sponsor category [1]
511
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Individual
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Name [1]
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Robert Schweitzer
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Address [1]
511
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Country [1]
511
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
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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 Esben Strodl
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Address
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School of Psychology and Counselling
Queensland University of Technology
Carsdeline Campus
Cnr Beams and Dorville Rds
Carseline QLD 4034
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Country
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Australia
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Phone
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+61 7 38644929
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Fax
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+61 7 38644755
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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 Esben Strodl
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Address
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School of Psychology and Counselling
Queensland University of Technology
Carsdeline Campus
Cnr Beams and Dorville Rds
Carseline QLD 4034
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Country
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Australia
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Phone
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+61 7 38644929
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Fax
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+61 7 38644755
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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.
Download to PDF