This study intends to use music and movement (MWM) to reduce anxiety and behavioral symptoms of people with early dementia (PWD) and their family carers in the community. It also aims to examine whether MWM can enhance the sleep quality of PWD and their family caregivers and promote their well-being. This is a mixed methods study with the quantitative paradigm being the main research approached used. The quantitative arm will be a randomized controlled trial (RCT). The qualitative arm will adopt a naturalistic approach through interviewing for data collection. Recruited subjects from the community centres of non-government organizations (NGOs) will be randomly allocated to the intervention and control group. The outcome measures of the PWD will include Rating Anxiety in Dementia (RAID), Geriatric Depression Scale (GDS), Neuropsychiatric Inventory Questionnaire (NPI-Q), Pittsburgh Sleep Quality Index (PQSI), Quality of Life - Alzheimer's Disease (QOL-AD), Mini-Mental State Examination (MMSE), Revised Life Event Scale (RLES), Modified Brathel Index (MBI) and Non-pharmacological Therapy Experience Scale (NPTES), whereas the outcome measures of the family caregivers will be Patient Health Questionnaire 9 (PHQ-9), Generalized Anxiety Disorder 7 (GAD-7), Zarit Burden Scale (ZBD), Pittsburgh Sleep Quality Index (PSQI), Reverse Life event Scale (RLES), and World Health Organization Quality of Life-BREF (WHOQOL-BREF). To address the research questions, data will be collected at baseline (T0), immediately post-intervention at 8-weeks (T1), and 8 post-intervention (T2). The qualitative arm of this study will contribute to the understanding of issues and effects of MWM as an intervention. Its finding will complement the results obtained from the RCT.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
95
Participants in the intervention group will receive the intervention delivered by their family member according to the validated 8-week music with movement (MWM) intervention protocol.
The control group will receive a protocol for social interaction as the control condition, where caregivers were asked to discuss up to date news with PWeD. The design of the control condition will be highly similar to the MWM protocol in terms of the frequency and duration of the sessions, the number of people involved, and the total intervention period.
The Hong Kong Polytechnic University
Hong Kong, Hong Kong
Change of Rating anxiety in Dementia (RAID)
For PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Geriatric Depression Scale (GDS)
For PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Neuropsychiatric Inventory Questionnaire(NPI-Q)
For PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Pittsburgh Sleep Quality Index (PQSI)
For PWD and Caregivers of PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Quality of Life - Alzheimer's Disease (QOL-AD)
For PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Patient Health Questionnaire 9 (PHQ-9)
For Caregivers of PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Zarit Burden Scale (ZBS)
For Caregivers of PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of World Health Organization Quality of Life-BREF (WHOQOL-BREF)
For Caregivers of PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Generalized Anxiety Disorder 7
For Caregivers of PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Mini-Mental State Examination (MMSE)
For PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Revised Life Event Scale (RLES)
For PWD and Caregivers of PWD Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Lawton's Instrumental Activity of Daily Living (IADL)
For PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
Change of Modified Barthel Index (MBI)
For PWD only Comparisons of changes of RAID will be considered as follows: 1. T1 - T0 2. T2 - T0 3. T2 - T1
Time frame: At baseline (T0), immediately post-intervention at 8-weeks (T1), and 8-weeks post-intervention (T2)
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