The dual-modal (face-to-face and online approaches), client-customized Caregivers Of dementia Processing Emotions (COPE) programme aims to 1. reduce caregivers' Expressed Emotion (EE), 2. reduce caregivers' depressive symptoms, 3. reduce the behaviourally interactive social dynamic of maladaptation (i.e., dysfunctional dyadic relationship and quality of care), and 4. improve caregivers' perceived stress from PwD's Behavioral and Psychological Symptoms of Dementia (BPSD). Researchers will compare COPE to a control group (standard therapy) to examine how effective the COPE programme is. Participants will take part in: Pretest prior to COPE implementation Post-test after COPE completion Follow up test in 3 months after COPE completion
Primary Purpose Prevention: Assessing the effectiveness of a novel intervention for preventing the development of negative outcomes in caregivers as a result of managing behavioral psychological symptoms of dementia. Interventional Study Model: Parallel: Participants are assigned to one of two groups in parallel for the duration of the study. Model Description: Participants are assigned to either COPE group or control group on a random basis. Baseline data are collected either face-to-face or online before the implementation. After six weeks of implementation, post-test data will be collected either face-to-face or online. Three months after post-test, follow-up data will be collected either face-to-face or online. Number of Arms: Two total arms, one for the COPE intervention group and one for the standard therapy control group. Masking: Participants Outcomes Assessors Allocation: Randomized: Participants are assigned to intervention groups by chance Enrollment: At least 56 subjects are needed for the two arms to allow the most accurate variance estimation for intervention of small to medium standardised effect size (0.2-0.6) at 80% power and 5% level of significance, with a 10% attrition rate. The social workers in the Psychogeriatric Day Hospital (Queen Mary Hospital) will refer the potential family caregivers of PwD to the RA for eligibility screening. Informed consent will be obtained accordingly.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
56
This is the first study to develop an easily accessible and feasible intervention programme, namely the Caregivers Of dementia Processing Emotions (COPE), to primarily reduce expressed emotion (EE) in family caregivers of PwD via processing one's attributional biases, dysregulated emotion, dysfunctional social dynamics using an integrative therapy. By displacing these negative thoughts and emotions, the integrative therapy has great potential to reduce the depressive symptoms in caregivers and thus mitigate their perceived stress from BPSD. In addition, the interactive social dynamics in the dementia caregiving context can be improved.
University of Hong Kong
Hong Kong, Hong Kong
RECRUITINGFamily Attitude Scale- Chinese Version
Measure caregivers' expressed emotions (EE) (i.e., criticism and hostility) held towards the PwD.
Time frame: From enrollment to the end of intervention at 7 weeks and end of study at 20 weeks.
Center of Epidemiological Studies of Depression Revised - Chinese Version
Assess caregivers' depression
Time frame: From enrollment to the end of intervention at 7 weeks and end of study at 20 weeks.
Dyadic Relationship Scale - Chinese Version
Evaluate caregivers' perspective of dyadic and family relationships in their daily caregiving activities
Time frame: From enrollment to the end of intervention at 7 weeks and end of study at 20 weeks.
Interaction Quality Scale - Chinese Version
Measure the quality of care.
Time frame: From enrollment to the end of intervention at 7 weeks and end of study at 20 weeks.
Neuropsychiatric Inventory - Chinese Version
Assess the severity of BPSD manifested in PwD reported by their caregivers.
Time frame: From enrollment to the end of intervention at 7 weeks and end of study at 20 weeks.
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