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Trial registered on ANZCTR
Registration number
ACTRN12613000778785
Ethics application status
Approved
Date submitted
10/07/2013
Date registered
11/07/2013
Date last updated
19/11/2019
Date data sharing statement initially provided
14/11/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Clinical and psychosocial changes over late childhood and adolescence and early life determinants of long term clinical outcomes in cystic fibrosis Study
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Scientific title
Clinical and psychosocial changes over late childhood and adolescence and early life determinants of long term clinical outcomes in cystic fibrosis Study
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Secondary ID [1]
282808
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Nil
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Universal Trial Number (UTN)
U1111-1145-4497
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Trial acronym
Follow-up ACFBAL Study (FAB) Study
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
cystic fibrosis
289582
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Condition category
Condition code
Human Genetics and Inherited Disorders
289916
289916
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0
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Cystic fibrosis
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Respiratory
289920
289920
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0
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Other respiratory disorders / diseases
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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
Two study visits will occur from 12 months up to 3 years depending on the timing of the initial visit. At each visit clinical data will be recorded including: current symptoms, physical examination, weight, height, concomitant medications, spirometry, induced sputum collection and urine for matrix breakdown products and biomarkers of neutrophilic inflammation. Blood is collected routinely for review tests and will be collected and stored for inflammatory mediators. Health Related Quality of Life questionnaires and other standard measures of psychosocial health are completed and a bone density test (a DEXA), and a low dose chest CT scan will be done at the start and end of the study (again this is depending on the timing of the initial visit).
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Intervention code [1]
287492
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Not applicable
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Comparator / control treatment
Not applicable - Observational study
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
289969
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Repeated measures of the FEV1 best annual values as SD-scores (z-scores) over the study duration using a calibrated spirometer. These data will have been collected at each clinic visit attended by the patient.
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Assessment method [1]
289969
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Timepoint [1]
289969
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3 years
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Primary outcome [2]
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CT scan scores. A low dose spirometer-controlled inspiratory and expiratory volumetric chest CT scans using a standard protocol will be performed without contrast at the start of the study and in the final year.
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Assessment method [2]
289970
0
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Timepoint [2]
289970
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3 years
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Primary outcome [3]
289971
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Association between the measures of Quality of Life and psychosocial functioning. The tests used are CFQ-R for parents and children and LSAC, . Parent social demographics, functioning and mental health (Brief COPE) will be done along with the Family Stress Scale. This is a composite primary outcome.
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Assessment method [3]
289971
0
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Timepoint [3]
289971
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3 years
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Secondary outcome [1]
303687
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Nil
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Assessment method [1]
303687
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Timepoint [1]
303687
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N/A
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Eligibility
Key inclusion criteria
All children with cystic fibrosis who completed the ACFBAL Study (ACTRN12605000665639)
CE Wainwright et al. Effect of Bronchoalveolar lavage-Directed Therapy on Pseudomonas aeruginosa Infection and Structural Lung Injury in Children with Cystic Fibrosis A Randomized Trial. JAMA 13 July 2011; 306(2): 163-171.
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Minimum age
9
Years
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Maximum age
15
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
Children who did not not complete the ACFBAL study
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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
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Statistical methods / analysis
The analyses will employ multivariable regression methods for which meaningful power calculations are difficult. However, the key questions addressed in these analyses will generally amount to comparisons of means between subgroups of the cohort, and indicative calculations can be made on that basis.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
15/07/2013
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Actual
1/08/2014
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Date of last participant enrolment
Anticipated
31/12/2018
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Actual
31/05/2019
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Date of last data collection
Anticipated
31/03/2019
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Actual
30/06/2019
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Sample size
Target
125
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Accrual to date
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Final
118
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC
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Recruitment hospital [1]
1231
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Royal Children's Hospital - Herston
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Recruitment hospital [2]
1233
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The Royal Childrens Hospital - Parkville
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Recruitment hospital [3]
1234
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The Children's Hospital at Westmead - Westmead
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Recruitment hospital [4]
1235
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Mater Children's Hospital - South Brisbane
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Recruitment hospital [5]
1236
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Womens and Childrens Hospital - North Adelaide
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Recruitment hospital [6]
1237
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John Hunter Hospital Royal Newcastle Centre - New Lambton
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Recruitment hospital [7]
1238
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Monash Medical Centre - Clayton campus - Clayton
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Recruitment hospital [8]
4692
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Lady Cilento Children's Hospital - South Brisbane
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Recruitment postcode(s) [1]
7144
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4029 - Royal Brisbane Hospital
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Recruitment postcode(s) [2]
7146
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3052 - Parkville
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Recruitment postcode(s) [3]
7148
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2145 - Westmead
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Recruitment postcode(s) [4]
7149
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4101 - South Brisbane
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Recruitment postcode(s) [5]
7150
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5006 - North Adelaide
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Recruitment postcode(s) [6]
7151
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2310 - Hunter Region
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Recruitment postcode(s) [7]
7152
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3800 - Monash University
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Recruitment postcode(s) [8]
12267
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4101 - Highgate Hill
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Recruitment outside Australia
Country [1]
5180
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New Zealand
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State/province [1]
5180
0
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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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National Health and Medical Research Council (NHMRC)
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Address [1]
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GPO Box 1421
Canberra
ACT 2601
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Country [1]
287586
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Australia
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Primary sponsor type
University
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Name
The University of Queensland
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Address
St Lucia
Queensland
4072
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Country
Australia
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Secondary sponsor category [1]
286333
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Government body
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Name [1]
286333
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Children's Health Hospital & Health Services
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Address [1]
286333
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Lady Cilento Children's Hospital
501 Stanley Street
South Brisbane 4101 QLD
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Country [1]
286333
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
289559
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Children’s Health Services Queensland Human Research Ethics Committee
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Ethics committee address [1]
289559
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Level 7 Centre for Children's Health Research Lady Cilento Children's Hospital 501 Stanley Street South Brisbane Queensland 4101
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Ethics committee country [1]
289559
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Australia
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Date submitted for ethics approval [1]
289559
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Approval date [1]
289559
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20/11/2012
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Ethics approval number [1]
289559
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HREC/12/QRCH/171
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Summary
Brief summary
The purpose of the study is to further improve outcomes in CF by developing a better understanding of the reasons for the decline in health status and lung function during adolescence, which is one of the key challenges facing clinicians. We hope to do this by looking at such things as the 1) pathology involved in CF lung disease, 2) long term risks of emerging organisms, 3)potential effects of early therapeutic interventions, such as P. aeruginosa eradication, 4) metagenomic profile identifying bacteria in respiratory samples, 5) psychosocial factors, and 6) relationship between early life events and outcomes between 9 - 17 years of age.
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Trial website
N/A
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Trial related presentations / publications
N/A
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Public notes
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Contacts
Principal investigator
Name
36966
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Prof Claire Wainwright
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Address
36966
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5a Dept. of Respiratory & Sleep Medicine
Lady Cilento Children's Hospital
501 Stanley Street
South Brisbane
QLD 4101
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Country
36966
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Australia
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Phone
36966
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+617 3068 1111
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Fax
36966
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+61 7 3068 2309
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Email
36966
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[email protected]
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Contact person for public queries
Name
36967
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Joyce Cheney
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Address
36967
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5a Dept. of Respiratory & Sleep Medicine
Lady Cilento Children's Hospital
501 Stanley Street
South Brisbane
QLD 4101
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Country
36967
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Australia
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Phone
36967
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+617 3069 7195
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Fax
36967
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+617 3069 7159
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Email
36967
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[email protected]
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Contact person for scientific queries
Name
36968
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Claire Wainwright
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Address
36968
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5a Dept. of Respiratory & Sleep Medicine
Lady Cilento Children's Hospital
501 Stanley Street
South Brisbane
QLD 4101
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Country
36968
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Australia
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Phone
36968
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+617 3068 1111
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Fax
36968
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+617 3068 2309
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Email
36968
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
A decision will be made on these matters in the coming months
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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
Dimensions AI
Early markers of cystic fibrosis structural lung disease: follow-up of the ACFBAL cohort
2020
https://doi.org/10.1183/13993003.01694-2019
N.B. These documents automatically identified may not have been verified by the study sponsor.
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