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Trial Review
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Trial registered on ANZCTR
Registration number
ACTRN12617000798369
Ethics application status
Approved
Date submitted
22/05/2017
Date registered
31/05/2017
Date last updated
13/09/2017
Type of registration
Prospectively registered
Titles & IDs
Public title
Caring for HEalthy Engaged Resilient staff: A wellness training program for emergency department nurses
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Scientific title
Caring for HEalthy Engaged Resilient staff: Effect of a wellness training program on stress in emergency department nurses
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Secondary ID [1]
292013
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
CHEER: Caring for HEalthy Engaged Resilient staff
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Stress
303399
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Coping
303400
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Condition category
Condition code
Alternative and Complementary Medicine
302812
302812
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0
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Spiritual care
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Those randomised to the intervention group will receive a face-to-face self-care intervention program designed and supervised by an accredited clinical psychologist with over 10 years of experience. Participants will be offered one of two weekly hospital based sessions of approximately 1 hour duration for 5 weeks (10 participants should be in each of the sessions) with a home program.
Sessions will cover the following topics;
Session 1
Phenomenology of Stress
How people cope – Support & Self Care
Self Care: 3 systems (Lifestyle, Physical (Body), Mental (Mind))
Lifestyle System: Sleep, Diet, Exercise, Fun
Principle of 5% change
Introduction to cyclic breathing – bridge to Session 2
Homework for session 1: Lifestyle audit, practice cyclic breathing
Session 2
Review Homework – Discussion
Physical System
Biological basis of arousal
Relaxation Training: overview, principles, goal (short and long techniques)
Skills training: cyclic breathing (review), Progressive Muscle Relaxation (PMR), Visualisation)
Homework for session 2: Progressive muscle relaxation, Visualisation
Session 3
Review Homework – Discussion
Mental System: Can’t stop thoughts, change how respond, shift focus of attention (Distraction), challenge (Cognitive Therapy), observe (Mindfulness)
Mindfulness: Definition
Skills Training - “mindfulness of the breath”
Homework for session 3: Practice – “mindfulness of the breath”
Session 4
Review Homework – Discussion
Mindfulness continued
Skills Training: “leaves on a stream”, mindful eating,
Homework for session 4: practice “leaves on a stream”, mindful eating
Session 5
Review Homework – Discussion
Cognitive Therapy: Overview, principles, ABC model
Discussion of process (techniques)
Discuss and work through brief examples
The sessions will be conducted in the ED conference room between the hours of 2pm and 3pm two afternoons per week. This time has been selected as it should minimise impact on clinical care and will also allow for completion of the program as part of work hours rather than in addition to current work schedule of already busy staff.
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Intervention code [1]
298143
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Lifestyle
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Intervention code [2]
298145
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Treatment: Other
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Comparator / control treatment
Control treatment = the control group will be placed on a wait list to commence the program 3 months following completion of the study
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Control group
Active
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Outcomes
Primary outcome [1]
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Stress will be measured using the Depression, Anxiety and Stress Scale-21
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Assessment method [1]
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Timepoint [1]
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7 Weeks and 3 Months post intervention commencement
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Secondary outcome [1]
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Professional Quality of Life will be measured using the Professional Quality of Life Scale, version 5 (Pro-QOL-5)
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Assessment method [1]
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Timepoint [1]
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7 Weeks and 3 Months post intervention commencement
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Secondary outcome [2]
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Program Attendance (self reported)
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Assessment method [2]
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Timepoint [2]
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7 Weeks post intervention commencement
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Secondary outcome [3]
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Work engagement will be measured using the Utrecht Work Engagement Scale (UWES)
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Assessment method [3]
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Timepoint [3]
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7 Weeks and 3 Months post intervention commencement
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Eligibility
Key inclusion criteria
Nurse currently rostered to work in the RBWH DEM
Able to attend program
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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?
Yes
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Key exclusion criteria
Regular meditation practice within the past 6 month period (greater than or equal to 1 session per week)
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Study design
Purpose of the study
Educational / counselling / training
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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)
An online randomisation procedure will be co-ordinated centrally by the research assistant using REDCap. By the end of accrual, it is planned to have approximately equal balance in each of the study groups.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
We will use blocked randomization to form the allocation list for the two comparison groups. We will use a computer random number generator to select random permuted blocks and an equal allocation ratio.
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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
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
All analysis will be carried out on an intention-to-treat basis. Participant characteristics will be summarised and compared using means and standard deviations. Differences in outcomes will be evaluated using contingency tables and chi-square test for proportions; differences in continuous variables between the two groups will be evaluated using student’s t-test or an appropriate non-parametric test if the data does not conform to assumptions of normality. Repeated measures analysis will be used for evaluating changes in depression, anxiety and stress at 7 weeks and 3 months.
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
23/10/2017
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Actual
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Date of last participant enrolment
Anticipated
30/10/2017
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Actual
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Date of last data collection
Anticipated
14/02/2018
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment hospital [1]
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Royal Brisbane & Womens Hospital - Herston
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Recruitment postcode(s) [1]
16129
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4029 - Royal Brisbane Hospital
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Recruitment postcode(s) [2]
16130
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4029 - Herston
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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This study is unfunded
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Address [1]
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Country [1]
296538
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Primary sponsor type
Hospital
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Name
Royal Brisbane and Women's Hospital
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Address
Butter field Street
Royal Brisbane and Women's Hospital
Herston QLD 4029
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Country
Australia
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Secondary sponsor category [1]
295493
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University
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Name [1]
295493
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Queensland University of Technology
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Address [1]
295493
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Cnr Musk and Victoria Park Road
Kelvin Grove QLD 4059
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Country [1]
295493
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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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Royal Brisbane and Women's Hospital
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Ethics committee address [1]
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Butterfield Street Block 7, Level 7 Royal Brisbane and Women's Hospital Herston QLD 4029
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Ethics committee country [1]
297758
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Australia
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Date submitted for ethics approval [1]
297758
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29/05/2017
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Approval date [1]
297758
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30/06/2017
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Ethics approval number [1]
297758
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HREC/17/QRBW/298
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Summary
Brief summary
Stress is very common in nursing and has a number of adverse consequences. The aim of this study is to pilot the feasibility of a brief workplace wellness intervention to emphasize the development of behaviours to strengthen the physical and mental health of emergency nurses. In this randomised controlled trial participants will be allocated to either control or intervention. The intervention group will receive a 5 week series of 1 hour classes guided by a Clinical Psychologist which teaches strategies to enhance resilience. Participants will be surveyed prior to starting the program, at the completion of the program and again 3 months later to assess the effect of the intervention on stress, professional quality of life, workplace engagement and resilience.
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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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Ms Carol Jeffers
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Address
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C/O Department of Emergency Medicine
Ground Floor, James Mayne Building
Butterfield Street
Royal Brisbane and Women's Hospital
Herston QLD 4029
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Country
75026
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Australia
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Phone
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+61 7 3646 7002
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Fax
75026
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Email
75026
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[email protected]
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Contact person for public queries
Name
75027
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James Hughes
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Address
75027
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C/O Department of Emergency Medicine
Ground Floor, James Mayne Building
Butterfield Street
Royal Brisbane and Women's Hospital
Herston QLD 4029
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Country
75027
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Australia
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Phone
75027
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+61 7 3646 4078
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Fax
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Email
75027
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[email protected]
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Contact person for scientific queries
Name
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James Hughes
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Address
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C/O Department of Emergency Medicine
Ground Floor, James Mayne Building
Butterfield Street
Royal Brisbane and Women's Hospital
Herston QLD 4029
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Country
75028
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Australia
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Phone
75028
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+61 7 3646 4078
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Fax
75028
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Email
75028
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[email protected]
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No information has been provided regarding IPD availability
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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