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Trial registered on ANZCTR
Registration number
ACTRN12606000111572
Ethics application status
Approved
Date submitted
24/03/2006
Date registered
29/03/2006
Date last updated
29/03/2006
Type of registration
Prospectively registered
Titles & IDs
Public title
A randomised controlled trial of a letter intervention in primary care patients to improve depression and anxiety disorders
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Scientific title
A randomised controlled trial of a letter intervention to assess psychiatric severity in primary care patients who have depressive and anxiety disorders
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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:
DSM-IV Axis 1 Depressive and Anxiety Disorders
1077
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Condition category
Condition code
Mental Health
1156
1156
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0
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Anxiety
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Mental Health
1157
1157
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0
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Depression
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Patients in experimental group receive a copy of the psychiatric assessment letter that is usually sent to the GP.
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Intervention code [1]
954
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Behaviour
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Comparator / control treatment
Control group participants will receive a thank-you letter only.
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Control group
Active
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Outcomes
Primary outcome [1]
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Severity of psychiatric condition
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Assessment method [1]
1557
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Timepoint [1]
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At baseline, 1 month and 3 months
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Secondary outcome [1]
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Adherence to treatment recommendations.
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Assessment method [1]
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Timepoint [1]
2804
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At 1 month and 3 months.
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Eligibility
Key inclusion criteria
Primary depressive or anxiety disorder.
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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
Substance abuse disorder, personality disorder, psychosis, risk of harm to self or others, unable to speak or read English, significant medical illness, incapable of consent, clinician discretion.
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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)
numbered containers
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
table of random numbers
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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
Factorial
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Other design features
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Phase
Phase 1
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/06/2006
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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
200
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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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Charities/Societies/Foundations
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Name [1]
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Beyondblue
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Address [1]
1264
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Country [1]
1264
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Australia
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Primary sponsor type
Hospital
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Name
The Alfred Hospital
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Address
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Country
Australia
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Secondary sponsor category [1]
1119
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None
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Name [1]
1119
0
Nil
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Address [1]
1119
0
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Country [1]
1119
0
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
The purpose of the study is to investigate whether patients who receive a copy of the psychiatric assessement letter that is sent to their GP have improved adherence to treatment recommendations. There are two hypotheses: 1. receiving the assessment report will improve patient adherence to treatment recommendations; 2. that receiving the assessment report will improve patient outcomes.
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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
36334
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Country
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Phone
36334
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Fax
36334
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Email
36334
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Contact person for public queries
Name
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Michael McGartland
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Address
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The Alfred Hospital
Commercial Rd
Prahran VIC 3181
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Country
10143
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Australia
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Phone
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+61 3 98044444
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Fax
10143
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Email
10143
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[email protected]
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Contact person for scientific queries
Name
1071
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Clare Graydon
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Address
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The Alfred Hospital
Commerical Rd
Prahran VIC 3181
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Country
1071
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Australia
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Phone
1071
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+61 3 98044444
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Fax
1071
0
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Email
1071
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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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