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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02911896
Registration number
NCT02911896
Ethics application status
Date submitted
25/07/2016
Date registered
22/09/2016
Titles & IDs
Public title
Physical Function in Critical Care (PaciFIC)
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Scientific title
Physical Function in Critical Care (PaciFIC): An Multi-centre Observational Study
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Secondary ID [1]
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2015026
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Universal Trial Number (UTN)
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Trial acronym
PaciFIC
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Intensive Care (ICU) Myopathy
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Condition category
Condition code
Musculoskeletal
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Observational
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Patient registry
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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
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Change in Physical Function in Intensive Care Test scored (PFIT-s) and De Morton Mobility Index from ICU awakening to hospital discharge
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Assessment method [1]
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Both measures are primary - there will be a single measure developed as composite in line with aims of this observational study
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Timepoint [1]
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Baseline to hospital discharge (up to 3 months)
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Eligibility
Key inclusion criteria
* Adults > 18 years of age
* Mechanically ventilated > 48 hours
* Premorbid able to ambulate at least 10m independently prior to ICU admission (+/- gait aid)
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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
* Premorbid physical or cognitive impairment which would prevent ability to perform functional measures
* New neurological impairment such as stroke or spinal cord injury
* Trauma or orthopaedic injury requiring period of immobilization or non weight bearing status
* Traumatic brain injury with focal neurology
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/08/2015
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/08/2017
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Sample size
Target
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Accrual to date
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Final
151
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Recruitment in Australia
Recruitment state(s)
SA,VIC
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Recruitment hospital [1]
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University of South Australia and Flinders Medical Centre - Adelaide
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Recruitment hospital [2]
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Royal Melbourne Hospital - Melbourne
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Recruitment postcode(s) [1]
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- Adelaide
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Recruitment postcode(s) [2]
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- Melbourne
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Recruitment outside Australia
Country [1]
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Brazil
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State/province [1]
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Brazil
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Country [2]
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Singapore
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State/province [2]
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Singapore
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Funding & Sponsors
Primary sponsor type
Other
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Name
University of Melbourne
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Address
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Country
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Other collaborator category [1]
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Other
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Name [1]
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Melbourne Health
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Address [1]
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Country [1]
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Other collaborator category [2]
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Government body
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Name [2]
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Flinders Medical Centre
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Address [2]
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Country [2]
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Other collaborator category [3]
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Other
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Name [3]
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National University Hospital, Singapore
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Address [3]
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Other collaborator category [4]
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Other
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Name [4]
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Escola Superior da Saude, Brazil
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Address [4]
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Country [4]
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Ethics approval
Ethics application status
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Summary
Brief summary
Impairment in physical function is a significant problem for survivors of critical illness. There is a growing urgency to develop a core set of outcome measures, which can be adopted in clinical and research practice to evaluate efficacy in response to interventions such as rehabilitation. Phase 1: Development of a new outcome measure. This study aims to examine the development of a single outcome measure which may be able to be utilised across the continuum of recovery of critical illness in the evaluation of physical function. The study will involve examination of two common physical function measures - the Physical Function in intensive care test scored (PFIT-s) and De Morton Mobility Index (DEMMI) and the development of a new measure based on rasch principles which may be able to capture physical functioning changes in individuals with critical illness. Aims: (1) To determine the clinical utility of two physical function measures (DEMMI and PFIT-s) when used in isolation across the hospital admission; and (2) To transform the (15-item) DEMMI and (4-item) PFIT-s into a single measure to evaluate function in intensive care survivors using Rasch analytical principles. Phase 2: Measurement properties of the PACIFIC physical function outcome measure in an independent validation sample.
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Trial website
https://clinicaltrials.gov/study/NCT02911896
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Trial related presentations / publications
Parry SM, Granger CL, Berney S, Jones J, Beach L, El-Ansary D, Koopman R, Denehy L. Assessment of impairment and activity limitations in the critically ill: a systematic review of measurement instruments and their clinimetric properties. Intensive Care Med. 2015 May;41(5):744-62. doi: 10.1007/s00134-015-3672-x. Epub 2015 Feb 5. Parry SM, Denehy L, Beach LJ, Berney S, Williamson HC, Granger CL. Functional outcomes in ICU - what should we be using? - an observational study. Crit Care. 2015 Mar 29;19(1):127. doi: 10.1186/s13054-015-0829-5.
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Public notes
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Contacts
Principal investigator
Name
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Dr Selina M Parry, PhD
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Address
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University of Melbourne
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Fax
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Undecided
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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
Type
Citations or Other Details
Journal
Parry SM, Granger CL, Berney S, Jones J, Beach L, ...
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Journal
Parry SM, Denehy L, Beach LJ, Berney S, Williamson...
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Results not provided in
https://clinicaltrials.gov/study/NCT02911896