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Trial registered on ANZCTR
Registration number
ACTRN12621000392864
Ethics application status
Approved
Date submitted
9/02/2021
Date registered
8/04/2021
Date last updated
20/10/2022
Date data sharing statement initially provided
8/04/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
Online mindfulness for people diagnosed with cancer (OM-C) study
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Scientific title
The feasibility, appropriateness, and acceptability of online mindfulness for people diagnosed with cancer (OM-C)
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Secondary ID [1]
303318
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None
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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:
cancer
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Condition category
Condition code
Cancer
318403
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0
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Any cancer
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will undertake an online seven-week mindfulness course. The course comprises online 90 minute face-to-face group classes held weekly using ZOOM. The number of participants per course will be 22 maximum, accounting for a 20% dropout rate. Course attendance will be recorded each week by the instructor. Each week different mindfulness techniques will be explained and experienced and this content is supported by course material (video, text and audio) provided via a web browser and accessible from any device. The course material can be accessed at the participant's leisure. Course content has been specifically developed for this study. All courses will be conducted by highly experienced teachers with 10-years plus mindfulness experience and training. Mindfulness teachers have experience in working with people with cancer.
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Intervention code [1]
319623
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Behaviour
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Intervention code [2]
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Lifestyle
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Comparator / control treatment
none
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Acceptability measured using the Acceptability of Intervention Measure
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Assessment method [1]
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Timepoint [1]
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7 weeks (course completion)
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Primary outcome [2]
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Appropriateness measured using the Appropriateness of Intervention Measure
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Assessment method [2]
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Timepoint [2]
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7 weeks (course completion)
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Primary outcome [3]
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Feasibility measured using the Feasibility of Intervention Measure
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Assessment method [3]
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Timepoint [3]
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7 weeks (course completion)
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Secondary outcome [1]
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Cancer symptom burden and severity assessed using the Edmonton Symptom Assessment Scale (ESAS)
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Assessment method [1]
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Timepoint [1]
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Baseline, 7 weeks (course completion)
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Secondary outcome [2]
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Depression, anxiety, and stress assessed using the DASS-21
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Assessment method [2]
391266
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Timepoint [2]
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Baseline, 7 weeks (course completion)
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Secondary outcome [3]
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Self-management skills assessed using the Health Education Impact Questionnaire
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Assessment method [3]
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Timepoint [3]
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Baseline, 7 weeks (course completion)
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Secondary outcome [4]
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Self-efficacy for coping with cancer, assessed using the Cancer Behavior Inventory
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Assessment method [4]
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Timepoint [4]
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Baseline, 7 weeks (course completion)
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Secondary outcome [5]
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Mindfulness assessed using the Freiburg Mindfulness Inventory
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Assessment method [5]
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Timepoint [5]
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Baseline, 7 weeks (course completion)
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Secondary outcome [6]
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Concerns and wellbeing of people affected by cancer assessed using the Measure Yourself Wellness and Concerns
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Assessment method [6]
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Timepoint [6]
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Baseline, 7 weeks (course completion)
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Eligibility
Key inclusion criteria
Any cancer, >6 month life expectancy
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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
Patients with high scores indicative of clinical levels of anxiety, or depression or a psychiatric diagnosis who are deemed unsuitable following further screening by the psychologist or health care professional
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
29/04/2021
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Actual
27/05/2022
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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
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Sample size
Target
108
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Accrual to date
87
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
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Chris O’Brien Lifehouse - Camperdown
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Recruitment postcode(s) [1]
38823
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2050 - Camperdown
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Chris O'Brien Lifehouse
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Address [1]
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119-143 Missenden Rd, Camperdown NSW 2050
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Country [1]
307734
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Australia
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Primary sponsor type
Hospital
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Name
Chris O'Brien Lifehouse
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Address
119-143 Missenden Rd, Camperdown NSW 2050
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Country
Australia
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Secondary sponsor category [1]
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University
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Name [1]
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Western Sydney University
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Address [1]
308435
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Locked Bag 1797 Penrith NSW 2751
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Country [1]
308435
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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St Vincent's Hospital Human Research Ethics Committee (HREC)
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Ethics committee address [1]
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390 Victoria Street Darlinghurst NSW 2010
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Ethics committee country [1]
307761
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Australia
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Date submitted for ethics approval [1]
307761
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Approval date [1]
307761
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02/12/2020
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Ethics approval number [1]
307761
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Summary
Brief summary
This trial aims to determine the acceptability, appropriateness, and feasibility of a 7-week online mindfulness course on individuals with a cancer diagnosis, and to evaluate its impact on coping and empowerment skills, cancer symptoms, and emotional wellbeing. Who is it for? You may be eligible for this study if you are 18 or above and have been diagnosed with cancer. Study details Participants will attend one 90-minute Zoom session per week, which will cover various mindfulness techniques and practices. Participants will also be given access to online course materials in the form of videos, text, and audio accessed online to support the content of the mindfulness course. A number of questionnaires will be given for completion before the course and at the end of the 7-week course as part of the study. It is hoped that this study may help to ascertain the main symptoms of cancer patients and whether mindfulness training is an acceptable, appropriate, and feasible way of effectively improving these symptoms.
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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
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Dr Suzanne Grant
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Address
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Chris O'Brien Lifehouse, 119-143 Missenden Rd, Camperdown NSW 2050
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Country
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Australia
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Phone
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+61 419126209
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Suzanne Grant
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Address
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Chris O'Brien Lifehouse, 119-143 Missenden Rd, Camperdown NSW 2050
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Country
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Australia
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Phone
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+61 2 8514 0000
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Suzanne Grant
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Address
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Chris O'Brien Lifehouse, 119-143 Missenden Rd, Camperdown NSW 2050
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Country
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Australia
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Phone
108400
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+61 2 8514 0000
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Fax
108400
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Email
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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
No additional documents have been identified.
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