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Trial registered on ANZCTR
Registration number
ACTRN12611001000998
Ethics application status
Approved
Date submitted
13/09/2011
Date registered
20/09/2011
Date last updated
27/03/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Meeting the education and support needs of women with breast cancer who are referred for radiotherapy: A multiple-baseline study
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Scientific title
The effect of a tailored educational intervention package (RT Prepare) on psychological distress levels in women with breast cancer who are referred for radiotherapy
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Secondary ID [1]
262963
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APP1006458 Cancer Australia
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Universal Trial Number (UTN)
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Trial acronym
RT Prepare
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Women diagnosed with breast cancer
270686
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Condition category
Condition code
Cancer
270860
270860
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0
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Breast
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Mental Health
270996
270996
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0
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Anxiety
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The tailored educational intervention package consists of: 1) a one-on-one consultation with a radiation therapist prior to treatment planning and 2) a one-on-one consultation with radiation therapist prior to first treatment. Prior to the introduction of this intervention, communication and consultation skills training will be provided to radiation therapists and they will be educated about what information to provide to patients at each time point. During the one to one consultations the radiation therapist will meet the patient for 20 minutes to discuss the procedure that is about to occur, what will be expected of the patient, any immediate discomfort or pain they should anticipate and any short or long term side efects that may result form the procedure.
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Intervention code [1]
269303
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Treatment: Other
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Comparator / control treatment
Usual care patients - Patients will be provided with the standard information that departments routinely provide at radiation planning and treatment.
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Control group
Active
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Outcomes
Primary outcome [1]
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Psychological distress measured using the Hospital Anxiety and Depression Scale.
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Assessment method [1]
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Timepoint [1]
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1) First appointment with their radiation oncologist 2) Following one on one consultation with a radiation therapist prior to treatment planning 3) Following one on one consultation with a radiation therapiston the first day of treatment. 4) Treatment completion.
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Secondary outcome [1]
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Specific concerns about radiotherapy measured by the Concerns about RT scale Short Form Health Survey
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Assessment method [1]
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Timepoint [1]
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1) First appointment with their radiation oncologist 2) Following one on one consultation with a radiation therapist prior to treatment planning 3) Following one on one consultation with a radiation therapiston the first day of treatment. 4) Treatment completion.
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Secondary outcome [2]
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patient knowledge of radiotherapy measured by the Knowledge of RT scale
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Assessment method [2]
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Timepoint [2]
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1) First appointment with their radiation oncologist 2) Following one on one consultation with a radiation therapist prior to treatment planning 3) Following one on one consultation with a radiation therapiston the first day of treatment. 4) Treatment completion.
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Secondary outcome [3]
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patient preparedness measured by the Cancer Treatment Survey
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Assessment method [3]
294042
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Timepoint [3]
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1) First appointment with their radiation oncologist 2) Following one on one consultation with a radiation therapist prior to treatment planning 3) Following one on one consultation with a radiation therapiston the first day of treatment. 4) Treatment completion.
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Secondary outcome [4]
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Patient general health as measured by the Short Form Health Survey (SF-12).
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Assessment method [4]
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Timepoint [4]
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1) First appointment with their radiation oncologist 2) Following one on one consultation with a radiation therapist prior to treatment planning 3) Following one on one consultation with a radiation therapiston the first day of treatment. 4) Treatment completion.
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Eligibility
Key inclusion criteria
Participants will be eligible for the study if they have been diagnosed with breast cancer, are about to commence a course of radiation therapy that will be more than 4 weeks, are over the age of 18, do not have cognitive impairement or psychiatric illness and are able to converse freely in English.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Patients who have commenced treatment or completed treatment planning and who have cognitive impairments or psychiatric illness.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
none
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
none
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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
Other
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Other design features
Multiple Baseline Study-All sites will initially collect data from usual care patients. Recruitment sites will then be randomly assigned to commence the intervention arm at different time points.
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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
Completed
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Date of first participant enrolment
Anticipated
1/01/2012
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Actual
28/07/2012
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Date of last participant enrolment
Anticipated
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Actual
10/01/2016
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Date of last data collection
Anticipated
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Actual
20/02/2016
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Sample size
Target
600
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Accrual to date
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Final
412
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Recruitment in Australia
Recruitment state(s)
VIC,SA,WA
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Recruitment hospital [1]
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Sir Charles Gairdner Hospital - Nedlands
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Recruitment hospital [2]
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Monash Medical Centre - Moorabbin campus - East Bentleigh
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Recruitment hospital [3]
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The Royal Adelaide Hospital - Adelaide
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Recruitment postcode(s) [1]
7380
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6009 - Nedlands
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Recruitment postcode(s) [2]
7381
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3165 - Bentleigh East
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Recruitment postcode(s) [3]
7382
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5000 - Adelaide
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Funding & Sponsors
Funding source category [1]
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Government body
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Name [1]
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Cancer Australia
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Address [1]
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Locked Bag 3 STRAWBERRY HILLS NSW 2012
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Country [1]
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Australia
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Funding source category [2]
269891
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Charities/Societies/Foundations
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Name [2]
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Beyond Blue
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Address [2]
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PO Box 6100 Hawthorn West, Victoria 3122
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Country [2]
269891
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Australia
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Primary sponsor type
Government body
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Name
Cancer Australia
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Address
Locked Bag 3 STRAWBERRY HILLS NSW 2012
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Country
Australia
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Secondary sponsor category [1]
268809
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None
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Name [1]
268809
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Address [1]
268809
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Country [1]
268809
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
271727
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Sir Charles Gairdner Human Research Ethics Committee
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Ethics committee address [1]
271727
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Sir Charles Gairdner Hospital Hospital Ave NEDLANDS WA 6009
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Ethics committee country [1]
271727
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Australia
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Date submitted for ethics approval [1]
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30/08/2011
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Approval date [1]
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16/11/2011
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Ethics approval number [1]
271727
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2011-130
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Ethics committee name [2]
271861
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Royal Adelaide Hospital Human Research Ethics Committee
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Ethics committee address [2]
271861
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Royal Adelaide Hospital North Terrace Adelaide SA 5000
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Ethics committee country [2]
271861
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Australia
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Date submitted for ethics approval [2]
271861
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30/08/2011
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Approval date [2]
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07/09/2011
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Ethics approval number [2]
271861
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110907
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Ethics committee name [3]
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Peter MacCallum Cancer Centre Human Research Ethics Committee
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Ethics committee address [3]
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Peter MacCallum Cancer Centre Level 4, 10 St Andrews Place East Melbourne, VIC 3002
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Ethics committee country [3]
271862
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Australia
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Date submitted for ethics approval [3]
271862
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15/10/2011
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Approval date [3]
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18/04/2012
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Ethics approval number [3]
271862
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11/93
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Ethics committee name [4]
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Curtin University Human Research Ethics Committee
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Ethics committee address [4]
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Office of Research and Development Curtin University GPO Box U 1987 Perth, Western Australia 6845
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Ethics committee country [4]
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Australia
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Date submitted for ethics approval [4]
289963
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08/08/2011
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Approval date [4]
289963
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10/10/2011
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Ethics approval number [4]
289963
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HR 123/2011
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Summary
Brief summary
This study aims to determine whether a tailored educational package can reduce psychological distress in women with breast cancer who are referred for radiotherapy. Who is it for? You may be eligible to join this study if you are a woman aged 18 years or more who has been diagnosed with breast cancer for which you are about to commence a course of radiation therapy that will be more than 4 weeks. Trial details Participants in this trial will be allocated to one of two groups. One group will receive the standard information provided in radiation oncology. The other group will undergo an innovative radiotherapy program, consisting of two one-on-one 20 minute educational sessions with their radiotherapist. During the consultations the radiation therapist will discuss the procedure that is about to occur, what will be expected of the patient, any immediate discomfort or pain they should anticipate, and any short or long term side effects that may result from the procedure. Participants will be assessed on four occasions before and after treatment to determine their psychological distress levels, specific concerns about radiotherapy, knowledge of radiotherapy, and preparedness for treatment.
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Trial website
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Trial related presentations / publications
Halkett, G., O'Connor, M., Aranda, S., Jefford, M., Merchant, S., York, D., Miller, L., & Schofield, P. (2016). Communication skills training for radiation therapists: preparing patients for radiation therapy. Journal of Medical Radiation Sciences, 63(4), 232-241. doi:10.1002/jmrs.171
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Georgia
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Address
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Faculty of Health Sciences Curtin University GPO Box U1987 Perth WA 6845
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Country
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Australia
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Phone
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+61 8 9266 1762
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Dr Georgia Halkett
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Address
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Faculty of Health Sciences Curtin University GPO Box U1987 Perth WA 6845
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Country
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Australia
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Phone
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+61 8 9266 1762
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Fax
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+61 8 9266 1770
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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 Georgia Halkett
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Address
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Curtin University GPO Box U1987 Perth WA 6845
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Country
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Australia
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Phone
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+61 8 9266 1762
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Fax
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+61 8 9266 1770
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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
Source
Title
Year of Publication
DOI
Embase
RT Prepare: A radiation therapist-delivered intervention reduces psychological distress in women with breast cancer referred for radiotherapy.
2018
https://dx.doi.org/10.1038/s41416-018-0112-z
N.B. These documents automatically identified may not have been verified by the study sponsor.
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