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Trial registered on ANZCTR
Registration number
ACTRN12614000636651
Ethics application status
Approved
Date submitted
6/06/2014
Date registered
17/06/2014
Date last updated
11/10/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Health Related Quality of Life in Malignant Mesothelioma
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Scientific title
An Observational Study of Health-related Quality of Life in People with Malignant Mesothelioma
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Secondary ID [1]
284736
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Nil
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Universal Trial Number (UTN)
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Trial acronym
HQOL in MM
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Malignant Mesothelioma
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Health Related Quality of Life
292091
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Anxiety
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Depression
292093
0
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Supportive Care Needs
292094
0
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Nutritional Status
292095
0
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Functional Status
292096
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Inflammatory Response
292097
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Condition category
Condition code
Cancer
292433
292433
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0
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Lung - Mesothelioma
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Mental Health
292484
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0
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Anxiety
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Mental Health
292485
292485
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0
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Depression
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Intervention/exposure
Study type
Observational
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Patient registry
True
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Target follow-up duration
2
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Target follow-up type
Years
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Description of intervention(s) / exposure
Participants involved in primary study will complete a range of patient reported outcome measures at 6-12 week intervals for up to 2 years. These measures will include assessment of health related quality of life, anxiety and depression and unmet supportive care needs. Optional sub-studies will involve nutritional assessment, functional assessment and donation of additional blood for the analysis of inflammatory markers.
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Intervention code [1]
289520
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Not applicable
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Comparator / control treatment
No control group or comparator will be observed during the course of this study.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Health related quality of life
Instrument(s): EORTC QLQ-C30 and LC13, LCSS-Meso
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Assessment method [1]
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Timepoint [1]
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Baseline, at regular follow up intervals (6-12 weeks) and following change in disease or treatment status for up to 2 years.
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Secondary outcome [1]
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Anxiety and Depression
Instrument(s): Hospital Anxiety and Depression Scale
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Assessment method [1]
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Timepoint [1]
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Baseline, at regular follow up intervals (6-12 weeks) and following change in disease or treatment status for up to 2 years.
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Secondary outcome [2]
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Functional Status
Instrument(s): 6 minute walk test
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Assessment method [2]
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Timepoint [2]
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Baseline, at regular follow up intervals (6-12 weeks) and following change in disease or treatment status for up to 2 years
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Secondary outcome [3]
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Nutritional Status
Instrument(s): Abridged Patient Generated Subjective Global Assessment (abPG-SGA) OR Patient Generated Subjective Global Assessment (PG-SGA), Skin Fold Measurements and Grip Strength
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Assessment method [3]
308696
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Timepoint [3]
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Baseline, at regular follow up intervals (6-12 weeks) and following change in disease or treatment status for up to 2 years.
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Secondary outcome [4]
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Inflammatory Response
Instrument(s): Serum level of cytokines
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Assessment method [4]
308697
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Timepoint [4]
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Baseline, and following change in disease or treatment status for up to 2 years.
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Secondary outcome [5]
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Glasgow Prognostic Score
Instrument(s): Albumin, CRP and NLR
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Assessment method [5]
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Timepoint [5]
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Baseline, at regular follow up intervals (6-12 weeks) and following change in disease or treatment status for up to 2 years.
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Secondary outcome [6]
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Supportive Care Needs
Instrument(s): Supportive Care Needs Survey Short Form (SCNS-34)
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Assessment method [6]
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Timepoint [6]
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Baseline, at regular follow up intervals (6-12 weeks) and following change in disease or treatment status for up to 2 years.
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Secondary outcome [7]
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Health Literacy
Instrument(s): Health Literacy 2 Single Item Questions
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Assessment method [7]
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Timepoint [7]
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Baseline, at regular follow up intervals (6-12 weeks) and following change in disease or treatment status for up to 2 years.
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Secondary outcome [8]
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Eastern Co-operative Oncology Group (ECOG) Performance Status
Instrument(s): Clinician rated
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Assessment method [8]
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Timepoint [8]
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Baseline, at regular follow up intervals (6-12 weeks) and following change in disease or treatment status for up to 2 years.
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Eligibility
Key inclusion criteria
1. Patients with a diagnosis of malignant mesothelioma
2. Able to comply with planned procedures and provide written evidence of informed consent
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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. Patients with insufficient English will be excluded from patient reported outcome component of the study but can still participate in the other aspects of the study.
2. People unavailable or unwilling to consent to ongoing follow-up
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Study design
Purpose
Psychosocial
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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
Primary analysis will describe the trajectory of change in Health-related Quality of Life from baseline by time and treatment group using linear mixed models.
Associations of secondary endpoints will be evaluated by entering each of the factors as time-varying covariates in separate linear mixed models.
Secondary endpoints will be evaluated in an exploratory, hypothesis-generating analysis to avoid over interpreting the data. They will be compared between treatment groups and possible relationships of these endpoints with Health-related Quality of Life assessed at baseline and at various points of treatment follow up. Correlation between each primary and secondary endpoint will be evaluated.
Change in Quality of Life during disease progression will be measured by a mean change score, calculated by subtracting patient baseline scores from the mean of their scores at follow-up. Between group differences will be summarised by the average of patient’s mean change scores and compared between with a mean change of zero using t-tests.
Multiple regression with be used to assess the effect of potential prognostic factors on Health-related Quality of Life.
Overall survival is an exploratory endpoint and will be described by the Kaplan-Meier method. A stratified log-rank test will be used to describe overall survival between the groups.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/05/2014
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Actual
22/05/2014
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Date of last participant enrolment
Anticipated
1/05/2017
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Actual
10/07/2017
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Date of last data collection
Anticipated
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Actual
31/10/2017
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Sample size
Target
200
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Accrual to date
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Final
105
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,QLD,SA,WA,VIC
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Recruitment hospital [1]
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Concord Repatriation Hospital - Concord
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Recruitment hospital [2]
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Royal Prince Alfred Hospital - Camperdown
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Recruitment hospital [3]
2589
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The Chris O’Brien Lifehouse - Camperdown
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Recruitment hospital [4]
2590
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Northern Cancer Institute - Frenchs Forest - Frenchs Forest
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Recruitment hospital [5]
2591
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Liverpool Hospital - Liverpool
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Recruitment hospital [6]
2592
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Campbelltown Hospital - Campbelltown
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Recruitment hospital [7]
2593
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Westmead Hospital - Westmead
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Recruitment hospital [8]
2594
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Prince of Wales Hospital - Randwick
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Recruitment hospital [9]
2595
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Calvary Mater Newcastle - Waratah
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Recruitment hospital [10]
2596
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Austin Health - Austin Hospital - Heidelberg
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Recruitment hospital [11]
2597
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Sir Charles Gairdner Hospital - Nedlands
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Recruitment hospital [12]
2598
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The Canberra Hospital - Garran
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Recruitment hospital [13]
2599
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Flinders Medical Centre - Bedford Park
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Recruitment hospital [14]
2600
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The Prince Charles Hospital - Chermside
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Recruitment hospital [15]
2601
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Nepean Hospital - Kingswood
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Recruitment hospital [16]
2602
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Sydney Adventist Hospital - Wahroonga
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Recruitment hospital [17]
2603
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The Queen Elizabeth Hospital - Woodville
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Recruitment hospital [18]
2604
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Dubbo Base Hospital - Dubbo
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Recruitment hospital [19]
2605
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Orange Health Service - Orange
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Recruitment postcode(s) [1]
8260
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2139 - Concord Repatriation Hospital
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Recruitment postcode(s) [2]
8261
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2050 - Camperdown
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Recruitment postcode(s) [3]
8263
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2050 - Missenden Road
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Recruitment postcode(s) [4]
8264
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2065 - St Leonards
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Recruitment postcode(s) [5]
8265
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2170 - Liverpool
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Recruitment postcode(s) [6]
8266
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2560 - Campbelltown
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Recruitment postcode(s) [7]
8267
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2145 - Westmead
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Recruitment postcode(s) [8]
8268
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2031 - Randwick
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Recruitment postcode(s) [9]
8269
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2298 - Waratah
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Recruitment postcode(s) [10]
8270
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3084 - Heidelberg
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Recruitment postcode(s) [11]
8271
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6009 - Nedlands
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Recruitment postcode(s) [12]
8272
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2605 - Garran
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Recruitment postcode(s) [13]
8273
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4032 - Chermside
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Recruitment postcode(s) [14]
8274
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2747 - Kingswood
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Recruitment postcode(s) [15]
8275
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2076 - Wahroonga
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Recruitment postcode(s) [16]
8276
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5011 - Woodville
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Recruitment postcode(s) [17]
8277
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2830 - Dubbo
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Recruitment postcode(s) [18]
8278
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2800 - Orange
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Funding & Sponsors
Funding source category [1]
289367
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Government body
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Name [1]
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Cancer Institue NSW
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Address [1]
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PO Box 41
Alexandria NSW 1435
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Country [1]
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Australia
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Primary sponsor type
University
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Name
The University of Sydney
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Address
Camperdown, NSW, 2006
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
288052
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Address [1]
288052
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Country [1]
288052
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Sydney Local Health District CRGH (EC00118)
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Ethics committee address [1]
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Concord Repatriation and General Hospital Level 1, Building 75 Hospital Road Concord NSW 2139
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
291133
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Approval date [1]
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16/08/2013
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Ethics approval number [1]
291133
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CH62/6/2013-092 J Vardy
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Summary
Brief summary
This study aims to describe the symptoms, quality of life and supportive care needs of people diagnosed with malignant mesothelioma (MM). Additionally, we aim to describe the nutritional and functional status of people with MM, and to assess the relationship between psychological factors (anxiety and depression) and quality of life and other outcomes. Who is it for? You may be eligible to joint this study if you are aged 18 years or more and have been diagnosed with malignant mesothelioma. Study details Participants in this study will be asked to complete a range of patient reported outcome measures at 6-12 week intervals for up to 2 years. These measures will include assessment of health related quality of life, anxiety and depression and unmet supportive care needs. Optional sub-studies will involve nutritional assessment, functional assessment and donation of additional blood for the analysis of inflammatory markers.
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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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A/Prof Janette Vardy
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Address
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Dept of Medical Oncology
Concord Repatriation General Hospital
Hospital Rd, Concord NSW 2139
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Country
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Australia
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Phone
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61297675000
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Fax
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61297679860
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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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Jason Fowler
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Address
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Asbestos Diseases Research Institute
PO Box 3628
Rhodes NSW 2138
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Country
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Australia
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Phone
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61297679847
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Fax
48955
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61297679860
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Email
48955
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[email protected]
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Contact person for scientific queries
Name
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Janette Vardy
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Address
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Dept of Medical Oncology
Concord Repatriation General Hospital
Hospital Rd, Concord NSW 2139
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Country
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Australia
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Phone
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61297675000
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Fax
48956
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61297679860
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Email
48956
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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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