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Trial registered on ANZCTR
Registration number
ACTRN12614000337673
Ethics application status
Approved
Date submitted
17/03/2014
Date registered
28/03/2014
Date last updated
5/05/2016
Type of registration
Retrospectively registered
Titles & IDs
Public title
Extracorporeal Membrane Oxygenation (ECMO) in adults: physical and mental health after hospitalisation.
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Scientific title
Physical and mental health outcomes in critically ill adults treated with Extracorporeal Membrane Oxygenation (ECMO) in Intensive Care Units (ICUs).
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Secondary ID [1]
284280
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Nil known
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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:
Extracorporeal membrane oxygenation for lung and or heart failure
291417
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Adult respiratory distress syndrome (ARDS)
291418
0
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Acute lung failure
291509
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Acute heart failure
291510
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Condition category
Condition code
Physical Medicine / Rehabilitation
291780
291780
0
0
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Other physical medicine / rehabilitation
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Mental Health
291781
291781
0
0
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Studies of normal psychology, cognitive function and behaviour
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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
Prospective observational study 3,6,12 and 18 months post discharge using quantitative surveys to assess health related quality of life and mental health followed by a limited number of semi-structured qualitative interviews with patients and relatives.
Patients will be surveyed once at 3,6,12 and 18 months after discharge.
Relatives that participate in the interviews will be surveyed once at the time of the interview.
10 interviews with patients and 10 interviews with relatives for approximate 1,5 hours each will be conducted 12 months after discharge from the hospital. Patients and relatives will be interviewed once only. Interviews will cover the experience of ECMO treatment before and after discharge.
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Intervention code [1]
288995
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Not applicable
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Comparator / control treatment
Patients treated with venous venous (VV) or venous arterial (VA) ECMO
Relatives
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
291706
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Health related quality of life, cognitive functioning; and depression, anxiety and post-traumatic stress disorder risk in patients 3 and 6 months after ECMO.
Short Form 36 Health survey (SF-36)
EQ-5D-5L survey (EQ-5D)
Hospital Anxiety and Depression Scale (HADS)
Telephone Interview for Cognitive Status (TICS)
Impact of Event Scale (revised) (IES-R)
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Assessment method [1]
291706
0
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Timepoint [1]
291706
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Separate at 3 and 6 months after ECMO
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Primary outcome [2]
291707
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Health related quality of life, cognitive functioning; and depression, anxiety and post-traumatic stress disorder risk in patients 12 and 18 months after ECMO.
Short Form 36 Health survey (SF-36)
EQ-5D-5L survey (EQ-5D)
Hospital Anxiety and Depression Scale (HADS)
Telephone Interview for Cognitive Status (TICS)
Impact of Event Scale (revised) (IES-R)
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Assessment method [2]
291707
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Timepoint [2]
291707
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Separate at 12 and 18 months after ECMO
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Primary outcome [3]
291734
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Patient's and relative's perception and experience with ECMO treatment
Exploration of themes that relate to patient's and relative's perception and experience with ECMO treatment and its impact on health outcomes via interviews using thematic analysis.
Interviews
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Assessment method [3]
291734
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Timepoint [3]
291734
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12 months after ECMO
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Secondary outcome [1]
307332
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Differences in survey scores between VV and VA subgroups
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Assessment method [1]
307332
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Timepoint [1]
307332
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Separate at 3,6,12 and 18 months after ECMO
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Eligibility
Key inclusion criteria
Patients who are 18 years or older, admitted to ICU and treated with ECMO from 2013 – 2014/15.
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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
Patients or relatives who do not speak English; cognitive / neurological impairments which would preclude completion of interviews or surveys; terminal conditions.
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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
Quantitative data: descriptive statistics
Qualitative data: thematic analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/05/2013
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Actual
15/05/2013
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Date of last participant enrolment
Anticipated
30/06/2014
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Actual
2/06/2014
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
30
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Accrual to date
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Final
24
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
2207
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The Alfred - Prahran
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Recruitment postcode(s) [1]
7886
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3004 - St Kilda Road Central
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Funding & Sponsors
Funding source category [1]
288907
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Other Collaborative groups
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Name [1]
288907
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Australian College of Critical Care Nurses
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Address [1]
288907
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Suite 1, 670 Canterbury Rd, Surrey Hills, Vic 3127
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Country [1]
288907
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Australia
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Primary sponsor type
Individual
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Name
Ralph Tramm
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Address
Australian and New Zealand Intensive Care Research Centre
Department of Epidemiology and Preventive Medicine
School of Public Health and Preventive Medicine
Monash University
The Alfred Centre, Level 6
99 Commercial Road
Melbourne VIC 3004
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Country
Australia
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Secondary sponsor category [1]
287602
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University
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Name [1]
287602
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Monash University,Department of Epidemiology and Preventive Medicine,School of Public Health and Preventive Medicine
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Address [1]
287602
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The Alfred Centre, Level 6
99 Commercial Road
Melbourne VIC 3004
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Country [1]
287602
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290737
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Alfred Ethics Committee
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Ethics committee address [1]
290737
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The Alfred OFFICE OF ETHICS & RESEARCH GOVERNANCE PO Box 315 Prahran VIC 3181
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Ethics committee country [1]
290737
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Australia
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Date submitted for ethics approval [1]
290737
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Approval date [1]
290737
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06/02/2013
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Ethics approval number [1]
290737
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555/12
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Summary
Brief summary
Prospective observational study 3,6,12 and 18 months post discharge using quantitative surveys to assess health related quality of life and mental health followed by a limited number of semi-structured qualitative interviews with patients and relatives.
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Trial website
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Trial related presentations / publications
A qualitative exploration of acute care and psychological distress experiences of ECMO survivors. Heart Lung. 2016 Feb 22. pii: S0147-9563(16)00011-X. doi: 10.1016/j.hrtlng.2016.01.010.
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Public notes
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Contacts
Principal investigator
Name
47010
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Dr Carol Hodgson
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Address
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Australian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine,Monash University
The Alfred Centre, Level 6
99 Commercial Road
Melbourne VIC 3004
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Country
47010
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Australia
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Phone
47010
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+61 3 990 30598
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Fax
47010
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Email
47010
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[email protected]
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Contact person for public queries
Name
47011
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Ralph Tramm
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Address
47011
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Australian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine,Monash University
The Alfred Centre, Level 6
99 Commercial Road
Melbourne VIC 3004
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Country
47011
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Australia
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Phone
47011
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+61 3 990 30932
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Fax
47011
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Email
47011
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[email protected]
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Contact person for scientific queries
Name
47012
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Ralph Tramm
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Address
47012
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Australian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine,Monash University
The Alfred Centre, Level 6
99 Commercial Road
Melbourne VIC 3004
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Country
47012
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Australia
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Phone
47012
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+61 3 990 30932
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Fax
47012
0
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Email
47012
0
[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
A qualitative exploration of acute care and psychological distress experiences of ECMO survivors.
2016
https://dx.doi.org/10.1016/j.hrtlng.2016.01.010
N.B. These documents automatically identified may not have been verified by the study sponsor.
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