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Trial registered on ANZCTR
Registration number
ACTRN12605000301662
Ethics application status
Approved
Date submitted
5/09/2005
Date registered
5/09/2005
Date last updated
5/09/2005
Type of registration
Retrospectively registered
Titles & IDs
Public title
A randomised controlled trial of a question prompt list for palliative care patients and their caregivers
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Scientific title
A randomised controlled trial of a question prompt list (QPL) for palliative care consultations, to evaluate the effect of the QPL on the total number of patient/caregiver questions during the consultation
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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:
Patients, and their cargeivers, with advanced progressive life limiting illnesses being referred for palliative care
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Condition category
Condition code
Other
461
461
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0
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Provision of a question prompt list (QPL) 20 minutes before palliative care consultation with physician endorsement of the QPL during consultation.
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Intervention code [1]
355
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Other interventions
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Comparator / control treatment
Controls received standard PC consultation
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Control group
Placebo
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Outcomes
Primary outcome [1]
522
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Total number of patient questions during the palliative care consultation (following provision of the question prompt list)
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Assessment method [1]
522
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Timepoint [1]
522
0
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Secondary outcome [1]
1117
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Total numbers of items discussed, patient concerns and caregiver questions/concerns during the consultation
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Assessment method [1]
1117
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Timepoint [1]
1117
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Secondary outcome [2]
1118
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Number of items discussed, patient/caregiver questions/concerns about 9 individual topics during the consultation
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Assessment method [2]
1118
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Timepoint [2]
1118
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Secondary outcome [3]
1119
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Achievement of patient information preferences
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Assessment method [3]
1119
0
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Timepoint [3]
1119
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24-hour/3-week follow up
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Secondary outcome [4]
1120
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Patient satisfaction with the consultation
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Assessment method [4]
1120
0
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Timepoint [4]
1120
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24-hour follow up
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Secondary outcome [5]
1121
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Patient anxiety
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Assessment method [5]
1121
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Timepoint [5]
1121
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24-hour/3-week follow up
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Secondary outcome [6]
1122
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Physician satisfaction with communication during the consultation
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Assessment method [6]
1122
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Timepoint [6]
1122
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24-hour follow up
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Secondary outcome [7]
1123
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Consultation duration.
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Assessment method [7]
1123
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Timepoint [7]
1123
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Eligibility
Key inclusion criteria
1) Diagnosis of advanced progressive life-limiting illness; 2) English-speaking; 3) able and well enough to read QPL and complete questionnaires; 4) seeing PC physician for either 1st, 2nd or 3rd consultation.
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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
No exclusion criteria
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Study design
Purpose of the study
Educational / counselling / training
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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)
Using sequentially numbered opaque sealed envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Block randomised in blocks using random number generator in Excel.
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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
Phase 3
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/10/2002
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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
160
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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]
513
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Government body
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Name [1]
513
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NHMRC postgraduate research scholarship
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Address [1]
513
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Country [1]
513
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Australia
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Primary sponsor type
University
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Name
Medical Psychology Research Unit, University of Sydney
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Address
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Country
Australia
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Secondary sponsor category [1]
420
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None
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Name [1]
420
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Nil
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Address [1]
420
0
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Country [1]
420
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1491
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Sydney University
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Ethics committee address [1]
1491
0
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Ethics committee country [1]
1491
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Australia
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Date submitted for ethics approval [1]
1491
0
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Approval date [1]
1491
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Ethics approval number [1]
1491
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Ethics committee name [2]
1492
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Royal Prince Alfred Hospital
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Ethics committee address [2]
1492
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Ethics committee country [2]
1492
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Australia
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Date submitted for ethics approval [2]
1492
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Approval date [2]
1492
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Ethics approval number [2]
1492
0
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Ethics committee name [3]
1493
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Concord Hospital
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Ethics committee address [3]
1493
0
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Ethics committee country [3]
1493
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Australia
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Date submitted for ethics approval [3]
1493
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Approval date [3]
1493
0
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Ethics approval number [3]
1493
0
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Ethics committee name [4]
1494
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St Vincent's Hospital
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Ethics committee address [4]
1494
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Ethics committee country [4]
1494
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Australia
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Date submitted for ethics approval [4]
1494
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Approval date [4]
1494
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Ethics approval number [4]
1494
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Ethics committee name [5]
1495
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Prince of Wales Hospital
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Ethics committee address [5]
1495
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Ethics committee country [5]
1495
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Australia
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Date submitted for ethics approval [5]
1495
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Approval date [5]
1495
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Ethics approval number [5]
1495
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Ethics committee name [6]
1496
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St George Hospital
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Ethics committee address [6]
1496
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Ethics committee country [6]
1496
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Australia
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Date submitted for ethics approval [6]
1496
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Approval date [6]
1496
0
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Ethics approval number [6]
1496
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Ethics committee name [7]
1497
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Calvary Hospital
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Ethics committee address [7]
1497
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Ethics committee country [7]
1497
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Australia
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Date submitted for ethics approval [7]
1497
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Approval date [7]
1497
0
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Ethics approval number [7]
1497
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Ethics committee name [8]
1498
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Nepean Hospital
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Ethics committee address [8]
1498
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Ethics committee country [8]
1498
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Australia
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Date submitted for ethics approval [8]
1498
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Approval date [8]
1498
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Ethics approval number [8]
1498
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Ethics committee name [9]
1499
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Liverpool Hospital
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Ethics committee address [9]
1499
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Ethics committee country [9]
1499
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Australia
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Date submitted for ethics approval [9]
1499
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Approval date [9]
1499
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Ethics approval number [9]
1499
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Ethics committee name [10]
1500
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Westmead Hospital
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Ethics committee address [10]
1500
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Ethics committee country [10]
1500
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Australia
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Date submitted for ethics approval [10]
1500
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Approval date [10]
1500
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Ethics approval number [10]
1500
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Ethics committee name [11]
1501
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Flinders Medical Centre
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Ethics committee address [11]
1501
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Ethics committee country [11]
1501
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Australia
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Date submitted for ethics approval [11]
1501
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Approval date [11]
1501
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Ethics approval number [11]
1501
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Summary
Brief summary
Patients being referred for palliative care have high levels of anxiety and significant informational and emotional needs. Previous research suggests these needs are not always met. Provision of a question prompt list (QPL) to cancer patients before initial oncology consultations has been found to promote patient question asking, reduce anxiety, improve recall and shorten the consultation. We have developed a QPL specifically for palliative care patients. We will study the effects of providing patients with this QPL before their consultation with a palliative care doctor.
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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
35630
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Address
35630
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Country
35630
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Phone
35630
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Fax
35630
0
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Email
35630
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Contact person for public queries
Name
9544
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Ms Rhonda Devine
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Address
9544
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Medical Psychology Research Unit
University of Sydney
Blackburn Building D06
Camperdown NSW 2006
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Country
9544
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Australia
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Phone
9544
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+61 2 90365380
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Fax
9544
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+61 2 90365420
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Email
9544
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[email protected]
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Contact person for scientific queries
Name
472
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Dr Josephine Clayton
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Address
472
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Medical Psychology Research Unit
University of Sydney
Blackburn Building D06
Camperdown NSW 2006
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Country
472
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Australia
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Phone
472
0
+61 2 90365289
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Fax
472
0
+61 2 9036 5292
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Email
472
0
[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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