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Trial registered on ANZCTR
Registration number
ACTRN12609000219280
Ethics application status
Approved
Date submitted
2/03/2009
Date registered
30/04/2009
Date last updated
17/12/2015
Type of registration
Retrospectively registered
Titles & IDs
Public title
Individualised nutritional counselling for patients who have undergone major upper gastrointestinal surgery - a randomised controlled trial
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Scientific title
A randomised controlled trial assessing weight change in individualised nutritional counselling for patients who have undergone major upper gastrointestinal surgery
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Secondary ID [1]
288179
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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:
Major Upper Gastrointestinal surgery
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Condition category
Condition code
Oral and Gastrointestinal
4651
4651
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Surgery
4652
4652
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0
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Other surgery
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Public Health
4975
4975
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0
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Health promotion/education
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
All patients will recieve a one-on-one 30 minute nutrition counselling session with a Dietitian on the ward prior to discharge to discuss eating after surgery. Basic information is covered such as small frequent meals and high energy/protein food choices. This is current practice. Then patients are randomised into a control group or intervention. The intevention group are contacted by the Dietitian by phone every 2 weeks for 6 months and face to face at 1 and 3 months. This nutrition couselling will include assessing intake, weight and symptoms, and giving relevant nutrition advice based on this.
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Intervention code [1]
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Behaviour
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Comparator / control treatment
Patients will recieve a one-on-one 30 minute nutrition counselling session with a Dietitian on the ward prior to discharge to discuss eating after surgery. Basic information is covered such as small frequent meals and high energy/protein food choices. This is current practice
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Control group
Active
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Outcomes
Primary outcome [1]
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Weight change - A Dietitian (seperate to the Dietitian giving nutrition counselling) will see the patient when they attend appointments with the consultant surgeon and weigh the patient.
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Assessment method [1]
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Timepoint [1]
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Data will be collected at 1, 3 and 6 months post discharge from hospital.
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Secondary outcome [1]
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Quality of life using the European Organisation for Research and treatment of Cancer Quality of Life Core Questionnaire (EORTC-QLQ-C30).
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Assessment method [1]
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Timepoint [1]
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1, 3 and 6 months post discharge from hospital
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Secondary outcome [2]
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Symptom Management (Gastrointestinal Symptom Rating Scale)
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Assessment method [2]
9291
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Timepoint [2]
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1, 3 and 6 months post discharge from hospital as per primary outcome.
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Eligibility
Key inclusion criteria
All patients undergoing Ivor-lewis Oesphagectomy, Partial or Total Gastrectomy, or Whipples surgery for non-neoplasm or curative neoplasm reasons.
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Minimum age
18
Years
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Maximum age
85
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
Known metastatic disease
Rural patient not to be followed up by Royal Prince Alfred Hospital (RPAH) surgeons
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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)
Patients will already be under the care of a Dietitian while in hospital. Prior to discharge they will be invited to participate in the study. If they agree to be involved baseline data will be collected (weight, Quality Of Life, symptoms) and baseline nutrition education will be given. Patient names for those that enrol in the study will be passed on to a third party who will randomise using numbered containers. The third party will pass the details of those allocated to the intervention on to the Dietitian responsible for nutrition counselling, while the orginal Dietitian who is responsible for collecting data will see every patient in the consultant surgeons rooms at 1,3 and 6 months.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Stratified randomisation according to type of surgery (oesphagectomy, gastrectomy and whipples), and then a simple randomisation based on a table from a text book.
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Masking / blinding
Blinded (masking 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
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
1/04/2009
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Actual
1/04/2009
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Date of last participant enrolment
Anticipated
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Actual
30/11/2011
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
50
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Accrual to date
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Final
30
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Sharon Lamb
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Address [1]
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Nutrition and Dietetics Department
Level 6, King George V (KGV) Building
Missenden Road
Royal Prince Alfred Hospital (RPAH)
Camperdown, NSW 2050
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Country [1]
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Australia
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Primary sponsor type
Hospital
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Name
Royal Prince Alfred Hospital
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Address
Nutrition and Dietetics Department
Level 6, King George V (KGV) Building
Missenden Road
Royal Prince Alfred Hospital (RPAH)
Camperdown, NSW 2050
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Country
Australia
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Secondary sponsor category [1]
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University
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Name [1]
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University of Sydney
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Address [1]
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University of Sydney
City Road
Camperdown, NSW 2006
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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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Royal Prince Alfred Hospital
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Ethics committee address [1]
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Research Development Office Level 3, Building 92 Missenden Road Royal Prince ALfred Hospital Camperdown, NSW 2050
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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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10/02/2009
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Approval date [1]
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01/03/2009
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Ethics approval number [1]
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HREC/09/RPAH/36
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Summary
Brief summary
Current practice is that once patients are discharged from hospital after surgery they do not have dietetic follow up. The aim of this study is to investigate whether individualised nutrition counselling improves nutritional status and quality of life in the 6 months post-discharge.
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Trial website
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Trial related presentations / publications
Carey S, Ferrie S, Ryan R, Beaton J, Young J and Allman-Farinelli M. Long term nutrition intervention following major upper gastrointestinal surgery – a prospective randomised controlled trial. European Journal of Clinical Nutrition, 2013,1-6.
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Public notes
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Contacts
Principal investigator
Name
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Dr Sharon Carey
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Address
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Nutrition and Dietetics
Royal Prince Alfred Hospital
Camperdown
NSW 2050
Australia
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Country
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Australia
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Phone
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+61295157863
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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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Sharon Lamb
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Address
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Nutrition and Dietetics Department
Level 6, King George V (KGV) Building
Missenden Road
Royal Prince Alfred Hospital (RPAH)
Camperdown, NSW, 2050
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Country
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Australia
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Phone
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+612 95157863
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Fax
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+612 9515 5047
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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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Sharon Lamb
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Address
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Nutrition and Dietetics Department
Level 6, King George V (KGV) Building
Missenden Road
Royal Prince Alfred Hospital (RPAH)
Camperdown, NSW, 2050
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Country
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Australia
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Phone
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+612 95157863
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Fax
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+612 95155047
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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