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Trial registered on ANZCTR
Registration number
ACTRN12606000215527
Ethics application status
Approved
Date submitted
24/05/2006
Date registered
31/05/2006
Date last updated
31/05/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
Improving continuity of clinical care and educating general practitioners – development and evaluation of information sheets about chemotherapy for general practitioners
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Scientific title
Improving continuity of clinical care and educating general practitioners – development and evaluation of information sheets about chemotherapy in patients with cancer for general practitioners
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Universal Trial Number (UTN)
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Trial acronym
GP Fax Sheets
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cancer (general)
1193
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Condition category
Condition code
Cancer
1278
1278
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0
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The intervention involves standardised faxed information (letter and drug information sheets) being sent to the GP of patients receiving chemotherapy at Peter Maccallum Cancer Centre. The faxed sheet will be one page long and sent immediately after the establishment of a baseline (a questionnaire testing GPs knowledge of their patients chemotherapy regime related side-effects administered directly after a patient begins their chemotherapy regime).
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Intervention code [1]
1069
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Other interventions
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Comparator / control treatment
The contol gorup will receive usual correspondance from Peter Maccallum, which consists of a non-standardised letter written by the patient's Medical Oncologist.
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Control group
Active
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Outcomes
Primary outcome [1]
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The primary outcome of the evaluation will be improved GP knowledge regarding management of patients having chemotherapy
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Assessment method [1]
1727
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Timepoint [1]
1727
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Measured one week after the administration of the intervention.
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Primary outcome [2]
1728
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The primary outcome of the evaluation will be improved self-perceived confidence regarding management of patients having chemotherapy
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Assessment method [2]
1728
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Timepoint [2]
1728
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Measured one week after the administration of the intervention.
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Secondary outcome [1]
3082
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For GPs – providing improved care for their patients on the basis of the consistent and comprehensive information provided.
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Assessment method [1]
3082
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Timepoint [1]
3082
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Secondary outcome [2]
3083
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For patients – enhanced care through more integrated health care delivery between Peter Mac and GPs and better-informed GPs. This might result in fewer uncontrolled side effects, and greater access to medical staff able to manage their side effects.
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Assessment method [2]
3083
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Timepoint [2]
3083
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Secondary outcome [3]
3084
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For Peter Mac – improved relationship with the GP community, fewer unplanned admissions due to inadequately controlled side effects, potentially fewer admissions of seriously unwell patients; more rapid triage of patients with life-threatening side effects such as febrile neutropenia. These outcomes will be measured at follow up one week after the administration of the intervemtion.
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Assessment method [3]
3084
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Timepoint [3]
3084
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Eligibility
Key inclusion criteria
To be eligible GPs must:1.Be the nominated GP of a patient with a defined cancer type, who is scheduled to commence a defined chemotherapy regimen 2.Agree to be randomised to either the intervention group who will receive faxed or e-mailed information or to the usual contact group3.Agree to participate in two brief telephone surveys (‘pre’ and ‘post’)4.Provide verbal informed consent to participate in this study
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Minimum age
Not stated
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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
To be eligible GPs must not:1.have already been enrolled in this study (if the same GP is treating two patients who are receiving chemotherapy in the Day Ward at Peter MacCallum Cancer Centre only the 1st patient will be included in this study)2. have a patient is is receiving concurrent radiotherapy.All age ranges and both genders will be included within the study.
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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)
Sealed Opaque Envelope Procedure
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Biased Coin Procedure
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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 1
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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
24/05/2006
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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
100
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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]
1400
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Commercial sector/Industry
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Name [1]
1400
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Roche Products
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Address [1]
1400
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Country [1]
1400
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Primary sponsor type
Charities/Societies/Foundations
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Name
Peter Macallum Cancer Centre
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Address
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Country
Australia
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Secondary sponsor category [1]
1230
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Commercial sector/Industry
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Name [1]
1230
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Roche Products
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Address [1]
1230
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Country [1]
1230
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Switzerland
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Peter Maccallum Cancer Centre
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Ethics committee address [1]
2752
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
2752
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Approval date [1]
2752
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Ethics approval number [1]
2752
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05/33
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Summary
Brief summary
The primary objective of this project is to demonstrate that the provision of information about chemotherapy and management of chemotherapy side effects 1.is perceived by GPs to be useful and, 2.when compared to usual care, results in (a)improved knowledge; (b)enhanced confidence regarding the management of patients having chemotherapy and (c)higher satisfaction with shared care with Peter Mac
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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
36216
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Country
36216
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Phone
36216
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Fax
36216
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Email
36216
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Contact person for public queries
Name
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Carl Baravelli
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Address
10258
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Educational Centre - Level 3, St Andrews Place East Melbourne Vic
Postal Address: Locked Bag 1 A'Beckett Street Victoria 8006
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Country
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Australia
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Phone
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+61 3 9656 1667
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Fax
10258
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+61 3 9656 1337
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Email
10258
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[email protected]
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Contact person for scientific queries
Name
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Carl Baravelli
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Address
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Educational Centre - Level 3 St Andrews Place East Melbourne VIC
Locked Bag 1 A'Beckett Street VIC 8006
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Country
1186
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Australia
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Phone
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+61 3 9656 1667
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Fax
1186
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+61 3 9656 1337
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Email
1186
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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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