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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT04892524
Registration number
NCT04892524
Ethics application status
Date submitted
7/05/2021
Date registered
19/05/2021
Titles & IDs
Public title
Virtual Management of Lung Nodules
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Scientific title
Investigation Into the Identification, Management and Follow-up of Incidental Lung Nodules.
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Secondary ID [1]
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SALHNLungNodules
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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:
Pulmonary Nodule, Solitary
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Pulmonary Nodule, Multiple
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Condition category
Condition code
Respiratory
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Other respiratory disorders / diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Other interventions - Virtual multidisciplinary review
Experimental: Virtual multidisciplinary review - Participants in this arm will be reviewed in a virtual clinic by a multidisciplinary team
No intervention: Face-to-face review - Participants in this group will be reviewed in a face-to-face clinic
Other interventions: Virtual multidisciplinary review
The virtual multidisciplinary review involves participants being reviewed by a multi-disciplinary team of specialist doctors, nurses and radiologists in a virtual environment. The team will analyse radiologic scans and make a recommendations for any follow-up scans, procedures or appointments that may be required
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Intervention code [1]
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Other interventions
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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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Cost
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Assessment method [1]
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Economic cost to participants and our health service, measured by an investigator-derived questionnaire asking participants to describe time spent engaging in the their health care and any direct costs associated with visits. Economical modelling will also be applied to determine the staffing and resource costs associated with provision of care to participants in each arm.
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Timepoint [1]
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6 months
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Secondary outcome [1]
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Participant satisfaction
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Assessment method [1]
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Participant satisfaction, measured by the Visit-Specific Satisfaction Instrument (VSQ-9)
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Timepoint [1]
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6 months
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Secondary outcome [2]
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Anxiety
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Assessment method [2]
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Participant anxiety as measure by the Hospital Anxiety and Depression Scale (HADS), which is a questionnaire containing seven items each for depression and anxiety subscales. Scoring for each item ranges from zero to three, with three denoting highest anxiety or depression level. A total subscale score of \>8 points out of a possible 21 denotes considerable symptoms of anxiety or depression.
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Timepoint [2]
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6 months
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Eligibility
Key inclusion criteria
* Age 18-80 years
* At least 1 IPN identified on CT imaging measuring 4-30 mm in maximal diameter
* CT slice thickness of 3 mm or less
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Minimum age
18
Years
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Maximum age
80
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
* Previous diagnosis of lung cancer
* History of haemoptysis
* Unexplained weight loss > 7 kg in the preceding 12 months
* Past history of malignancy within 5 years (excluding non-melanoma skin cancer)
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Study design
Purpose of the study
Other
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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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
Parallel
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Other design features
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Phase
NA
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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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
19/04/2021
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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
1/10/2023
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Actual
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Sample size
Target
55
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
SA
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Recruitment hospital [1]
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Flinders Medical Centre - Bedford Park
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Recruitment postcode(s) [1]
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5042 - Bedford Park
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Funding & Sponsors
Primary sponsor type
Other
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Name
Southern Adelaide Local Health Network
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
This is a study to determine how a virtual model for the management of lung nodules compares to a face-to-face clinic for patient satisfaction, quality of life and cost.
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Trial website
https://clinicaltrials.gov/study/NCT04892524
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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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Anand Rose
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Address
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Southern Adelaide Local Health Network
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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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Country
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Phone
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Fax
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Email
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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)?
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
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT04892524