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Trial registered on ANZCTR
Registration number
ACTRN12612000974808
Ethics application status
Approved
Date submitted
25/08/2012
Date registered
10/09/2012
Date last updated
10/09/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
Peer delivered support intervention for people who hear voices: Pilot randomised controlled trial
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Scientific title
Effect of a peer delivered support intervention for people who hear voices on subjective impact of voices
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Secondary ID [1]
281093
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Nil
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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:
Auditory verbal hallucinations
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Schizophrenia
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Psychotic disorders
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Condition category
Condition code
Mental Health
287573
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0
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Schizophrenia
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will receive 12 weekly one hour one-to-one sessions of a support intervention for hearing voices (auditory verbal hallucinations) from a peer mental health worker who has had personal lived experience of hearing voices themselves. The intervention will involve buidling a shared understanding of the participant's experience of hearing voices and using this to inform how to respond to hearing voices and cope with this experience more effectively. The intervention group will receive the intervention alongside treatment as usual (TAU) in the 3 month period immediately following randomisation, whilst the control group will receive the intervention after a 3 month TAU wait list period.
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Intervention code [1]
285545
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Behaviour
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Comparator / control treatment
Treatment as usual (wait list). The control group will receive the intervention after a 3 month treatment as usual wait list period. Treatment as usual will involve the person's usual mental health care which will oridinarily include prescription of antipsychotic medication, plus meetings with mental health workers and possible attendence at rehabilitative and recovery-oriented mental health service programmes. Participants in current receipt of formal psychological interventions will not be eligible to participate. Antipsychotic medication prescribing will be tracked in both conditions and chlorpromazine-equivalent dosages controlled for in analyses if needed.
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Control group
Active
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Outcomes
Primary outcome [1]
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Subjective Experiences of Psychosis Scale
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Assessment method [1]
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Timepoint [1]
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Baseline, 3 months (post-intervention), 6 months (follow-up)
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Secondary outcome [1]
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Psychotic Symptom Rating Scales - Auditory Hallucinations
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Assessment method [1]
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Timepoint [1]
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baseline, 3 months, 6 months
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Secondary outcome [2]
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Recovery Assessment Scale
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Assessment method [2]
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Timepoint [2]
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Baseline, 3 months, 6 months
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Eligibility
Key inclusion criteria
Auditory verbal hallucinations at least weekly over the past six months associated with significant distress or disability
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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
Recent (past 8 weeks) or planned change in antipsychotic medication
Currently receiving individual psychological therapy
Insufficient English or intellectual functioning to meaningfully participate
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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)
Treatment allocation made independently via email
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computerised sequence generation
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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Other design features
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Phase
Not Applicable
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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
1/11/2012
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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
35
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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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Recruitment postcode(s) [1]
5735
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3004
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Recruitment postcode(s) [2]
5736
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3141
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Recruitment postcode(s) [3]
5737
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3181
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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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John T Reid Charitable Trust
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Address [1]
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PO Box 438
Canterbury VIC 3128
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Country [1]
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Australia
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Primary sponsor type
Hospital
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Name
Monash Alfred Psychiatry Research Centre
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Address
The Alfred
Commercial Road
Melbourne VIC 3004
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Country
Australia
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Secondary sponsor category [1]
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Charities/Societies/Foundations
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Name [1]
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Prahran Mission
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Address [1]
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Chapel Street
PO Box 68
Prahran VIC 3181
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Alfred HREC
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Ethics committee address [1]
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Office of Research and Governance The Alfred Commercial Road Melbourne VIC 3004
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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27/08/2012
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Approval date [1]
287907
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Ethics approval number [1]
287907
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Summary
Brief summary
Hearing voices (auditory verbal hallucination) is a potentially distressing and disabling experience which often persists in spite of treatment with medication. This pilot study examines whether it is helpful for people who hear voices to receive assistance in coping with this experience from someone else who hears voices and has adapted to living with this experience.
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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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Ms Indigo Daya
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Address
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Voices Vic
15 Cromwell Road
South Yarra VIC 3141
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Country
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Australia
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Phone
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+61 3 9692 9562
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Fax
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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 Neil Thomas
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Address
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Monash Alfred Psychiatry Research Centre
Level 3, 607 St Kilda Road
Melbourne VIC 3004
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Country
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Australia
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Phone
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+61 3 9076 6564
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Fax
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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