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Trial registered on ANZCTR
Registration number
ACTRN12618000012279
Ethics application status
Approved
Date submitted
30/11/2017
Date registered
10/01/2018
Date last updated
11/12/2018
Date data sharing statement initially provided
11/12/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Positive Expiratory Pressure Therapy Recorder for Assessing Compliance (PEPtrac) - Initial Evaluation in Adults with Cystic Fibrosis..
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Scientific title
Positive Expiratory Pressure Therapy Recorder for Assessing Compliance (PEPtrac) - Initial Evaluation in adults with Cystic Fibrosis.
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Secondary ID [1]
293495
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None
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Universal Trial Number (UTN)
U1111-1206-0053
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Trial acronym
PEPtrac-1
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cystic Fibrosis
305679
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Condition category
Condition code
Human Genetics and Inherited Disorders
304900
304900
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0
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Cystic fibrosis
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will use the PEPtrac device attached and operating with either the PariPEP S, Aerobika or Acapella DH. Participants will be able to choose which one of the three devices they would like to use. Recruitment is limited to 6 participants per device. Participants will perform at least one treatment session per day over the one week study period. Participants may elect to do more than one treatment session per day if clinically indicated based on participant self-assessment and/or physiotherapist opinion. There is no upper limit to the number of treatment sessions able to be performed each day. Treatments will be self-administered at home. The PariPEP will be used for 6 sets of 15 breaths, aiming for a mid-expiratory pressure of 10-20cmH2O. The Aerobika and Acapella will be used for 4 sets of 15 breaths, with a resistance setting than allows a slightly active expiration with inspiratory:expiratory ratio of 1:3-4. Treatment sessions will last approximately 15 minutes. The PEPtrac will be operating in 'research' mode which means participants do not see the duration of treatment or pressures recorded. Participants will also complete a treatment diary entry at the end of each treatment session, recording the start and finish times and number of breaths and cycles performed.
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Intervention code [1]
299732
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Treatment: Devices
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Comparison of the PEPtrac data versus participant self-reports via a treatment diary for number of recorded sessions.
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Assessment method [1]
304094
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Timepoint [1]
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After one week of treatment
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Primary outcome [2]
304172
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Comparison of the PEPtrac data versus participant self-reports via a treatment diary for number of recorded breaths and cycles for each treatment session.
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Assessment method [2]
304172
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Timepoint [2]
304172
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After one week of treatment
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Secondary outcome [1]
340937
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Participant reported ease of use of the PEPtrac via purpose-specific questionnaire developed by the investigators.
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Assessment method [1]
340937
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Timepoint [1]
340937
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After one week of treatment.
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Eligibility
Key inclusion criteria
Diagnosis of cystic fibrosis, attending the Royal Adelaide Hospital Adult Cystic Fibrosis Service
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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
Unable to provide informed consent, inability to understand written English, post lung transplantation, recent positive culture of Burkholderia cepacia or Non-Tuberculosis Mycobacteria, current inpatient, current participation in an interventional trial where modification of their airway clearance technique would be considered a protocol violation, any condition which is considered a contraindication to PEP/OPEP therapy.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation is not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Not applicable
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
Participants will be able to choose which airway clearance device they use with the PEPtrac. A maximum of 6 participants may use each time of airway clearance device.
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
A sample of convenience was selected for this initial exploratory study.(n=18). Data will be summarised descriptively. Systematic differences and variability will be determined by plotting differences between the PEPtrac recordings and participant diaries for: number of treatment sessions recorded and with-in treatment data (treatment duration, number of cycles, number of breaths).
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
29/01/2018
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Actual
16/02/2018
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Date of last participant enrolment
Anticipated
30/06/2018
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Actual
25/09/2018
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Date of last data collection
Anticipated
7/07/2018
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Actual
2/10/2018
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Sample size
Target
18
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Accrual to date
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Final
18
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Recruitment in Australia
Recruitment state(s)
SA
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Recruitment hospital [1]
9470
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The Royal Adelaide Hospital - Adelaide
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Recruitment postcode(s) [1]
18197
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5000 - Adelaide
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Funding & Sponsors
Funding source category [1]
298112
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Hospital
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Name [1]
298112
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The Royal Adelaide Hospital
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Address [1]
298112
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Port Road
Adelaide
SA 5000
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Country [1]
298112
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Australia
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Funding source category [2]
298113
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University
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Name [2]
298113
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La Trobe University
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Address [2]
298113
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Plenty Rd & Kingsbury Drive
Bundoora
Vic 3086
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Country [2]
298113
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Australia
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Primary sponsor type
Individual
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Name
Nathan Ward
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Address
c/o Physiotherapy
8E055.08
The Royal Adelaide Hospital
Port Road
Adelaide
SA 5000
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Country
Australia
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Secondary sponsor category [1]
297192
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Individual
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Name [1]
297192
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Kathy Stiller
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Address [1]
297192
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7F060
Royal Adelaide Hospital
Port Road
Adelaide
SA 5000
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Country [1]
297192
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Australia
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Secondary sponsor category [2]
297193
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Individual
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Name [2]
297193
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Bruce Ward
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Address [2]
297193
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University of Adelaide
School of Physical Sciences
North Terrace
Adelaide
SA 5000
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Country [2]
297193
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Australia
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Secondary sponsor category [3]
297194
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Individual
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Name [3]
297194
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Amanda Kenyon
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Address [3]
297194
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c/o Physiotherapy
8E055.08
Royal Adelaide Hospital
Port Road
Adelaide
SA 5000
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Country [3]
297194
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Australia
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Secondary sponsor category [4]
297195
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Individual
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Name [4]
297195
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Prof Anne Holland
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Address [4]
297195
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La Trobe University Clinical School
Alfred Health
Level 4
The Alfred Centre
99 Commercial Rd
Melbourne
Vic 3004
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Country [4]
297195
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
299131
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Royal Adelaide Hospital Human Research Ethics Committee
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Ethics committee address [1]
299131
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Level 4 Women's Health Centre Royal Adelaide Hospital North Terrace Adelaide SA 5000
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Ethics committee country [1]
299131
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Australia
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Date submitted for ethics approval [1]
299131
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09/11/2017
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Approval date [1]
299131
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24/11/2017
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Ethics approval number [1]
299131
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HREC/17/RAH/270
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Ethics committee name [2]
299132
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La Trobe University University Human Ethics Committee
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Ethics committee address [2]
299132
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David Myers East Level 2, 224 La Trobe University Plenty Rd and Kingsbury Drive Bundoora Vic 3086
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Ethics committee country [2]
299132
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Australia
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Date submitted for ethics approval [2]
299132
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11/12/2017
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Approval date [2]
299132
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Ethics approval number [2]
299132
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Ethics committee name [3]
299243
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University of Adelaide Human Research Ethics Committee
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Ethics committee address [3]
299243
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Research Services University of Adelaide North Terrace Adelaide SA 5005
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Ethics committee country [3]
299243
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Australia
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Date submitted for ethics approval [3]
299243
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07/12/2017
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Approval date [3]
299243
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14/12/2017
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Ethics approval number [3]
299243
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32307
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Summary
Brief summary
This trial aims to determine the ability of the PEPtrac to record airway clearance sessions performed at home by adults with cystic fibrosis utilising commonly used positive pressure airway clearance devices when compared to participant self-reports. Participants will use the PEPtrac and an airway clearance device for a one week period, performing a treatment session at least once daily At the completion of each treatment session, participants will complete a treatment diary entry. After one week, participants will also complete a questionnaire examining their experience of using the PEPtrac and any suggested design modifications that they may have.
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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
79406
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Mr Nathan Ward
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Address
79406
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c/o Physiotherapy
8E055.08
Royal Adelaide Hospital
Port Road
Adelaide
SA 5000
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Country
79406
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Australia
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Phone
79406
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+61 8 7074 2855
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Fax
79406
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Email
79406
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[email protected]
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Contact person for public queries
Name
79407
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Nathan Ward
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Address
79407
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c/o Physiotherapy
8E055.08
Royal Adelaide Hospital
Port Road
Adelaide
SA 5000
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Country
79407
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Australia
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Phone
79407
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+61 8 7074 2855
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Fax
79407
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Email
79407
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[email protected]
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Contact person for scientific queries
Name
79408
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Nathan Ward
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Address
79408
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c/o Physiotherapy
8E055.08
Royal Adelaide Hospital
Port Road
Adelaide
SA 5000
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Country
79408
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Australia
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Phone
79408
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+61 8 7074 2855
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Fax
79408
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Email
79408
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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
Collated results on participant feedback will be presented. Individual treatment session data may be presented in future presentations/publications.
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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
No additional documents have been identified.
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