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Trial registered on ANZCTR
Registration number
ACTRN12621001175864
Ethics application status
Approved
Date submitted
28/07/2021
Date registered
1/09/2021
Date last updated
1/09/2021
Date data sharing statement initially provided
1/09/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
ECLIPSE: A pilot study of an early intervention to empower and support care partners of individuals with Alzheimer’s disease.
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Scientific title
ECLIPSE: A pilot study investigating the impact of a group educational intervention on quality of life in partners of individuals with Alzheimer’s disease
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Secondary ID [1]
304908
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None
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Universal Trial Number (UTN)
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Trial acronym
ECLIPSE
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Alzheimer's
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Condition category
Condition code
Neurological
320614
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0
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Alzheimer's disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Interested care partners of people with mild Alzheimer’s disease will participate in the study. Four small-group sessions will be facilitated. The sessions will be held weekly via videoconference with up to 12 participants in total. Session attendance checklists will be used to monitor adherence to the intervention.
ECLIPSE will follow the COPE framework of Creativity, Optimism, Planning and Expert Information to develop problem-solving skills and awareness of stressors. Session topics will be derived from collaboration with a Consumer Advisory Group. Broadly, the emphasis will be:
1. Psychoeducation
2. Symptoms and changes
3. Strategies to manage changes
4. Self-care for care partners
Each session will be of approximately one and a half hours duration, and cover a particular topic. The sessions will be a mixture of information provided by experts in the field, group-led discussion based on care partner’s personal experiences, and interactive learning and development of new skills to assist them in their care partner role.
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Intervention code [1]
321302
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Prevention
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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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Mean quality of life score, as measured by the Adult Carer Quality of Life Questionnaire (AC-QoL)
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Assessment method [1]
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Timepoint [1]
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Baseline, Post-intervention, and 3 months post-intervention.
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Primary outcome [2]
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Mean coping strategies score, as measured by the Brief-COPE
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Assessment method [2]
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Timepoint [2]
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Baseline, Post-intervention, and 3 months post-intervention.
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Secondary outcome [1]
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Mean caregiver burden core, as measured by the Caregiver Burden Scale and Caregiver Reaction Scale
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Assessment method [1]
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Timepoint [1]
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Baseline, Post-intervention, and 3 months post-intervention.
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Secondary outcome [2]
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Mean confidence of Alzheimer's knowledge score, as measured by the Alzheimer's disease knowledge scale
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Assessment method [2]
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Timepoint [2]
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Baseline, post-intervention and 3 months post-intervention
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Secondary outcome [3]
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Mean stress score as measured by Kingston Care partner stress scale
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Assessment method [3]
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Timepoint [3]
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Baseline, post-intervention and 3 months post-intervention
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Secondary outcome [4]
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Mean life satisfaction score, as measured by Life Satisfaction Questionnaire
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Assessment method [4]
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Timepoint [4]
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Baseline, post-intervention and 3 months post-intervention
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Secondary outcome [5]
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Mean anxiety symptomatology score, as measured by Depression, Anxiety and Stress Scale
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Assessment method [5]
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Timepoint [5]
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Baseline, post-intervention and 3 months post-intervention
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Secondary outcome [6]
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Mean depressive symptomatology score, as measured by the Depression, Anxiety and Stress Scale.
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Assessment method [6]
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Timepoint [6]
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Baseline, post-intervention and 3 months post-intervention
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Eligibility
Key inclusion criteria
(i) Are aged 18 years or older
(ii) Identify as being a care partner of an individual with mild Alzheimer’s disease.
(iii) Engage in at least four hours of contact care per week.
(iv) Have been a care partner for no longer than five years.
(v) Are competent to consent based on their ability to provide a spontaneous narrative description of the key elements of the study.
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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
Have participated in a care partner support intervention within the past six months.
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Study design
Purpose of the study
Prevention
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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
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/09/2021
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Actual
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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
12
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Funding & Sponsors
Funding source category [1]
309283
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Charities/Societies/Foundations
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Name [1]
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Epworth Medical Foundation
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Address [1]
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888 Toorak Road, Camberwell VIC 3124
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Monash University
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Address
Wellington Rd
Clayton
VIC 3800
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
310253
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Monash Health
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Ethics committee address [1]
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Level 2, I Block Monash Medical Centre 246 Clayton Road Clayton Victoria 3168
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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15/06/2021
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Ethics approval number [1]
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Summary
Brief summary
The care partner of a person with Alzheimer’s disease can be as much a “client” of a health service as a patient. They are heavily involved in facilitating the treatment and engagement of a patient, and thus need to be supported in this role that may have been unexpectedly thrust upon them. Care partner burnout has been identified as one of the main reasons individuals with dementia enter long-term care, therefore early intervention to support and empower care partners is critical. Interventions for care partners of individuals with a chronic illness have been shown to improve the psychological wellbeing of care partners. However, few empirical studies have been completed on the benefits of early intervention for care partners of individuals with Alzheimer’s disease. ECLIPSE - a newly designed, weekly, small-group-based intervention - will be provided over a four-week period to care partners of individuals recently diagnosed with Alzheimer’s disease. This project aims to implement and evaluate the effectiveness of ECLIPSE to improve psychological wellbeing, and to empower and support care partners.
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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 Melanie Emonson
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Address
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Epworth Centre for Innovation in Mental Health
888 Toorak Road
Camberwell VIC 3124
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Country
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Australia
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Phone
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+61 398054346
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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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Melanie Emonson
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Address
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Epworth Centre for Innovation in Mental Health
888 Toorak Road
Camberwell VIC 3124
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Country
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Australia
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Phone
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+61 398054346
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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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Melanie Emonson
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Address
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Epworth Centre for Innovation in Mental Health
888 Toorak Road
Camberwell VIC 3124
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Country
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Australia
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Phone
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+61 398054346
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Fax
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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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