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Trial registered on ANZCTR
Registration number
ACTRN12618000716268
Ethics application status
Approved
Date submitted
24/04/2018
Date registered
1/05/2018
Date last updated
1/09/2020
Date data sharing statement initially provided
1/09/2020
Type of registration
Retrospectively registered
Titles & IDs
Public title
The Prospective Athlete Heart Study- elucidating genetic determinants of cardiac remodelling using endurance exercise as an environmental stress.
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Scientific title
The Prospective Athlete Heart Study- elucidating genetic determinants of cardiac remodelling using endurance exercise as an environmental stress.
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Secondary ID [1]
294706
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None
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Universal Trial Number (UTN)
U1111_1212_8349
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Trial acronym
Pro@Heart
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Linked study record
ACTRN12618000711213
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Health condition
Health condition(s) or problem(s) studied:
Cardiac Remodelling
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Athlete's Heart
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Heart Failure
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Genetics
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Cardiac arrythmia's
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Condition category
Condition code
Cardiovascular
306641
306641
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0
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Normal development and function of the cardiovascular system
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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
A prospective comparison of endurance athletes and non-athletes which will assess the primary hypothesis that rare variants in 65 genes associated with abnormalities of cardiac structure will be more prevalent in those athletes with the greatest cardiac remodelling after 2 years of intense endurance exercise training.
All subjects will undergo detailed assessment of cardiac structure and exercise capacity at baseline, after two years, 5 years and every 5 years after that for 25years total.
Testing will include, anthropometry measures (height, weight, BP), echocardiogram, electrocardiogram, 24h holter monitoring, Cardiac Magnetic Resonance Imaging with exercise, VO2 max test, 12 month exercise diary, blood samples, Dexa scan.
Selection for genotyping after 2 years.
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Intervention code [1]
300999
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Diagnosis / Prognosis
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Comparator / control treatment
Endurance exercise represents the ideal model for testing genetic–environmental interactions. Therefore endurance athletes will be compared to a non-athletic control group.
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Control group
Active
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Outcomes
Primary outcome [1]
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Assess the prevalence of rare variants in cardiac structural genes relative to Left Ventricular Mass index in endurance athletes and non-athletes by performing next generation sequencing in 65 cardiac genes extracting DNA from circulating white cells.
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Assessment method [1]
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Timepoint [1]
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2 years after baseline testing
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Primary outcome [2]
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left ventricular mass index (LVMi) on cardiac magnetic resonance imaging (CMR)
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Assessment method [2]
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Timepoint [2]
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2 years after baseline testing
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Secondary outcome [1]
346005
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Assess the changes in cardiac structure (cardiac mass and geometry) by measurement of LV and RV volumes and myocardial mass using cardiac magnetic resonance (CMR) with gadolinium contrast
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Assessment method [1]
346005
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Timepoint [1]
346005
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baseline, 2 years
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Secondary outcome [2]
346007
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Assess fitness status by VO2 max (measurement of maximum oxygen metabolism) test on bicycle ergometer with metabolic cart
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Assessment method [2]
346007
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Timepoint [2]
346007
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baseline, two years, 5 years and every 5 years after that for 25 years.
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Secondary outcome [3]
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Assess the prevalence of cardiac arrhythmia's on electrocardiogram and 24h holter monitoring
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Assessment method [3]
346137
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Timepoint [3]
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baseline, two years, 5 years and every 5 years after that for 25 years
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Secondary outcome [4]
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Assessment of myocardial fibrosis using T1-weighted inversion recovery times on cardiac MRI
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Assessment method [4]
346139
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Timepoint [4]
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Baseline and 2 years
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Secondary outcome [5]
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Measurement of torsion, strain and strain rate using transthoracic echocardiogram, including Doppler and 3D volumetric acquisitions.
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Assessment method [5]
346140
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Timepoint [5]
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baseline, 2 years
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Secondary outcome [6]
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Blood samples to measure fasting lipid profile, cardiac biomarkers (Troponin I, Brain Natriuretic Peptide), Hs_CRP, FBE and U&E.
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Assessment method [6]
346141
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Timepoint [6]
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baseline, two years
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Secondary outcome [7]
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Resting blood pressure and blood pressure response during exercise measured in office after lying supine for 10 minutes and during the VO2 max test
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Assessment method [7]
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Timepoint [7]
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baseline, 2 years
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Secondary outcome [8]
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Measurement of body composition and bone mineral density by a dual energy X-ray absorptiometry (DEXA) scan (whole body, spine and hip scan)
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Assessment method [8]
346144
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Timepoint [8]
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baseline, two years.
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Secondary outcome [9]
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Quantify exercise duration and intensity during one week from self-report on an exercise diary or by recording on an electronic fitness device
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Assessment method [9]
346147
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Timepoint [9]
346147
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baseline, two years
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Eligibility
Key inclusion criteria
Endurance athletes, male and female, aged 16-23 years, competing in endurance sports in which aerobic fitness conditioning is a principal component of performance. Aiming to be involved in competition and high level training for more than 5 years.
Non-athletes, male and female, aged 16-23 years, less than 2 hours of endurance activity per week, not competing in an endurance sport, not enrolled in a fitness program to improve fitness.
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Minimum age
16
Years
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Maximum age
23
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
- Known cardiovascular disease
- Cigarette smoking (current or previous)
- Moderate or severe hypertension.
- Use of performance enhancing drugs.
- A contraindication to magnetic resonance imaging
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Study design
Purpose
Screening
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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
Prospective exercise cohort (320 athletes; 220 males, 100 females)
Non-athletic controls (110 males, 50 females)
The reason for recruiting a cohort of approximately two-thirds male is a pragmatic balance between opportunities for recruitment, given greater male participation in endurance sport, balanced against the opportunity to provide female athletic data which is under-represented in the scientific literature.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
23/05/2016
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Date of last participant enrolment
Anticipated
31/12/2020
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Actual
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Date of last data collection
Anticipated
31/12/2044
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Actual
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Sample size
Target
480
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Accrual to date
140
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Final
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Recruitment in Australia
Recruitment state(s)
SA,VIC
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Recruitment hospital [1]
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Baker Heart and Diabetes Institute - Melbourne
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Recruitment hospital [2]
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South Australian Health and Medical Research Institute (SAHMRI) - Adelaide
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Recruitment postcode(s) [1]
22518
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3004 - Melbourne
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Recruitment postcode(s) [2]
22519
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5000 - Adelaide
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Recruitment outside Australia
Country [1]
10351
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Belgium
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State/province [1]
10351
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Antwerp, Brabant
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Funding & Sponsors
Funding source category [1]
299311
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Government body
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Name [1]
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NHMRC APP1109322
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Address [1]
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Research Committee Secretariat NHMRC GPO Box 1421 Canberra ACT 2601
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Country [1]
299311
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Australia
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Funding source category [2]
299315
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Charities/Societies/Foundations
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Name [2]
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National Heart Foundation
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Address [2]
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2/850 Collins St, Melbourne VIC 3008
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Country [2]
299315
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Australia
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Primary sponsor type
Other
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Name
Baker Heart and Diabetes Institute
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Address
99 Commercial Road
Melbourne
VIC 3004
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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]
298580
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Address [1]
298580
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Country [1]
298580
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
300221
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Alfred Hospital Ethics Committee
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Ethics committee address [1]
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55 Commercial Road Melbourne VIC 3004
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Ethics committee country [1]
300221
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Australia
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Date submitted for ethics approval [1]
300221
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23/07/2015
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Approval date [1]
300221
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21/10/2015
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Ethics approval number [1]
300221
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333/15
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Summary
Brief summary
The heart can be stimulated to change its size and shape. The heart changing size and shape is a normal adaptation; however, in certain cases this adaptation can become harmful. Change in heart structure predicts heart events (eg. congestive heart failure, abnormal heart beats). Heart size and shape varies considerably between people; it is currently unknown what accounts for most of this variability. Previous studies suggest a genetic contribution; however, no studies have yet identified the specific changes in a person’s genetic makeup which explain why one person has a bigger heart than another. This study aims to identify rare variants in specific genes that are related to abnormal changes in heart structure. This study will do so by tracking changes in heart structure related to endurance exercise training as well as normal aging. Endurance athletes with the greatest change in heart structure will have select genes compared to endurance athletes with the least change in heart structure after 2 years of training. Additionally these gene profiles will be compared to non-endurance athletes who have the greatest and least change in heart structure over a 2-year period. In this way investigators can identify which gene variants are related to highly adaptive versus less adaptive hearts. Identifying gene variants related to heart size may help identify individuals at risk of abnormalities in which the heart enlarges too much. Identifying at-risk individuals allows doctors to identify people who may benefit from advice or treatments that may prevent problems from developing.
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Trial website
https://www.baker.edu.au/research/clinical-trials/pro-heart-trial
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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 Andre La Gerche
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Address
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Baker Heart and Diabetes Institute
Alfred Centre, level 4
99 commercial Road
Melbourne
VIC 3004
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Country
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Australia
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Phone
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+61 3 8532 1169
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Fax
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Email
82962
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[email protected]
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Contact person for public queries
Name
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Kristel Janssens
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Address
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Baker Heart and Diabetes Institute
Alfred Centre, level 4
99 commercial Road
Melbourne
VIC 3004
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Country
82963
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Australia
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Phone
82963
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+61 3 8532 1169
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Fax
82963
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Email
82963
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[email protected]
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Contact person for scientific queries
Name
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Andre La Gerche
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Address
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Baker Heart and Diabetes Institute
Alfred Centre, level 4
99 commercial Road
Melbourne
VIC 3004
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Country
82964
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Australia
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Phone
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+61 3 8532 1169
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Fax
82964
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Email
82964
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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
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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
Embase
Rationale and design of the PROspective ATHletic Heart (Pro@Heart) study: Long-term assessment of the determinants of cardiac remodelling and its clinical consequences in endurance athletes.
2022
https://dx.doi.org/10.1136/bmjsem-2022-001309
N.B. These documents automatically identified may not have been verified by the study sponsor.
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