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Trial registered on ANZCTR
Registration number
ACTRN12618000190202
Ethics application status
Approved
Date submitted
8/01/2018
Date registered
7/02/2018
Date last updated
7/02/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Multidisciplinary assessment at dialysis entry (MADE) study
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Scientific title
Multidisciplinary assessment at dialysis entry (MADE) study measuring quality of life, psychological, gastrointestinal, nutritional, frailty and health literacy measures in patients with end stage kidney disease commencing haemodialysis or peritoneal dialysis
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Secondary ID [1]
293725
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None
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Universal Trial Number (UTN)
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Trial acronym
MADE
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
End Stage Kidney Disease
306079
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Haemodialysis
306080
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Peritoneal Dialysis
306081
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Condition category
Condition code
Renal and Urogenital
305213
305213
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0
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Kidney disease
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Survey of participants at the commencement of dialysis with follow up surveys at 3 and 6 months. The survey includes a 159 item questionnaire and 2 physical function tests. The questionnaire is paper based, given to the participant by a researcher when they attend dialysis and collected the next dialysis treatment 2 days following. The participant completes it independently. The questionnaire combines 12 validated questionnaires. The two physical function tests are grip strength as measured by dynamometer and 3 metre up and go test. Each test takes 2 minutes to complete and is undertaken in the dialysis clinic prior to the patient attending dialysis. There is no intervention in this study.
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Intervention code [1]
299976
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Early Detection / Screening
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Quality of Life change as measured Integrated Palliative care Outcome Scale (IPOS Renal)
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Assessment method [1]
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Timepoint [1]
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0, 3 and 6 months
Primary time point is 6 months
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Secondary outcome [1]
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Depression, Anxiety and Stress as measured by the Depression, Anxiety and Stress Scale (DASS21) and the Emotional Thermometer
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Assessment method [1]
341751
0
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Timepoint [1]
341751
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0, 3 and 6 months
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Secondary outcome [2]
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Illness Perception as measured by the Brief Illness Perception Questionnaire (BILP)
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Assessment method [2]
341753
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Timepoint [2]
341753
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0, 3 and 6 months
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Secondary outcome [3]
341754
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Coping Abilities as measure by the "Brief COPE' scale
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Assessment method [3]
341754
0
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Timepoint [3]
341754
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0,3 and 6 months
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Secondary outcome [4]
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Perceptions of Illness Intrusion as measured by the Illness Intrusive Rating Scale
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Assessment method [4]
341755
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Timepoint [4]
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0,3 and 6 months
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Secondary outcome [5]
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Dietary Habits as measured by the Weekly Food Checklist
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Assessment method [5]
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Timepoint [5]
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0, 3 and 6 months
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Secondary outcome [6]
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Gastrointestinal Health as measured by the Gastrointestinal Symptom Rating Scale (GSRS) and Bristol Stool Chart
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Assessment method [6]
342521
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Timepoint [6]
342521
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0, 3 and 6 months
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Secondary outcome [7]
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Sleep Quality as measured by the The Pittsburgh Sleep Quality Index (PSQI)
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Assessment method [7]
342522
0
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Timepoint [7]
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0. 3 and 6 months
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Secondary outcome [8]
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Medication Adherence as measured by the Morisky Medication Adherence Scale
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Assessment method [8]
342523
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Timepoint [8]
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0, 3 and 6 months
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Secondary outcome [9]
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Health literacy as measured by the BRIEF Health Literacy Screening Tool.
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Assessment method [9]
342524
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Timepoint [9]
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0, 3 and 6 months
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Secondary outcome [10]
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Cognition as measured by the Montreal Cognitive Assessment (MOCA) Tool
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Assessment method [10]
342525
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Timepoint [10]
342525
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0, 3 and 6 months
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Secondary outcome [11]
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Physical function as measured by the 3 meter up and go test
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Assessment method [11]
342769
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Timepoint [11]
342769
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0, 3 and 6 moths
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Secondary outcome [12]
342770
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Grip Strength as measured by Dynamometer
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Assessment method [12]
342770
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Timepoint [12]
342770
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0,3 and 6 months
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Eligibility
Key inclusion criteria
1. End Stage Kidney Disease
2. Commencing haemodialysis or peritoneal dialysis
3. Commencing in the Central Northern Area Renal and Transplant Service (CNARTS)
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Minimum age
18
Years
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Maximum age
No limit
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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
1. Acute Kidney Disease only
2. Commencing dialysis in a rural clinic
3. Unable to understand English
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Categorical data will be analysed using chi-squared tests (or Fisher’s exact test for small samples). This data will be analysed using a repeated measures analysis of variance (ANOVA) with time being the dependent variable.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
7/12/2017
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Date of last participant enrolment
Anticipated
30/06/2018
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Actual
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Date of last data collection
Anticipated
31/12/2018
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Actual
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Sample size
Target
160
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Accrual to date
7
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Final
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Recruitment in Australia
Recruitment state(s)
SA
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Recruitment hospital [1]
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The Royal Adelaide Hospital - Adelaide
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Recruitment hospital [2]
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The Queen Elizabeth Hospital - Woodville
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Recruitment hospital [3]
9692
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Hampstead Rehabilitation Centre - Northfield
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Recruitment postcode(s) [1]
18459
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5000 - Adelaide
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Recruitment postcode(s) [2]
18460
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5011 - Woodville
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Recruitment postcode(s) [3]
18461
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5085 - Northfield
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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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Kidney, Transplant & Diabetes Research Australia (KTDRA)
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Address [1]
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1 Port Road, Adelaide, South Australia, 5000
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Country [1]
298340
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Australia
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Primary sponsor type
Hospital
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Name
Royal Adelaide Hospital
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Address
1 Port Road, Adelaide, South Australia, 5000
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Country
Australia
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Secondary sponsor category [1]
297675
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None
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Name [1]
297675
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None
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Address [1]
297675
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Country [1]
297675
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
299332
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Royal Adelaide Hospital Human Research Ethics Committee
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Ethics committee address [1]
299332
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Level 4, Women’s Health CentreRoyal Adelaide Hospital North TerraceAdelaide, South Australia, 5000
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Ethics committee country [1]
299332
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Australia
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Date submitted for ethics approval [1]
299332
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24/10/2017
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Approval date [1]
299332
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31/10/2017
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Ethics approval number [1]
299332
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HREC/17/RAH/467
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Summary
Brief summary
The aim of the study is to better identify the care needs of individuals with end stage kidney disease commencing dialysis. Commencing dialysis impacts individuals beyond their physical health. Participants will be asked to complete a questionnaire and undergo physical function tests over the first 6 months of their dialysis treatment. Quality of life, psychological and physical function, gastro-intestinal health, nutrition and health literacy will be measured. Results of this study will help inform the development of this standard protocol and allow for modifications to be developed to address the needs of patients.
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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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Dr Shilpa Jesudason
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Address
80086
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Room 7F401, Royal Adelaide Hospital, 1 Port Road, Adelaide, SA, 5000
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Country
80086
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Australia
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Phone
80086
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+61870742558
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Fax
80086
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Email
80086
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[email protected]
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Contact person for public queries
Name
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Paul Bennett
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Address
80087
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7F401, Royal Adelaide Hospital, 1 Port Road, Adelaide, SA, 5000
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Country
80087
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Australia
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Phone
80087
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+61870742558
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Fax
80087
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Email
80087
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[email protected]
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Contact person for scientific queries
Name
80088
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Paul Bennett
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Address
80088
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7F401, Royal Adelaide Hospital, 1 Port Road, Adelaide, SA, 5000
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Country
80088
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Australia
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Phone
80088
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+61870742558
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Fax
80088
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Email
80088
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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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