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Music Attuned Technology for Care via eHealth – MATCH - Study 2

Not Applicable
Completed
Conditions
behavioural symptoms of dementia
psychological symptoms of dementia
Agitation
Neurological - Dementias
Neurological - Alzheimer's disease
Neurological - Other neurological disorders
Registration Number
ACTRN12622000193774
Lead Sponsor
The University of Melbourne
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
36
Inclusion Criteria

Inclusion criteria of people living with dementia:
•Home co-habiting with at least one other person who nominates to be the primary caregiver.
•No age limits are stipulated so people with early onset of dementia may also be included.
•Formal diagnosis of Mild Cognitive Impairment or Dementia.

Inclusion Criteria of Family Caregivers:
•close in relationship to the person living with dementia
•co-habiting with the person with dementia.

Exclusion Criteria

•Dyads where there is no access to the internet or a mobile device where the app needs to be downloaded and accessed for study participation.
•Hearing impairment that is not overcome by hearing support such as hearing aids for both family carer and person living with dementia
•The carer does not have good knowledge of English. This is because the first minimum viable product is a mobile app version with basic features and only in English. Versions in other languages should be available as intermediate or advanced features in the mobile app.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Effectiveness of implementation of MATCH Music Training Program in the management of behavioural and psychological symptoms of dementia, assessed by changes in Neuropsychiatric Inventory Questionnaire (NPI-Q) between baseline and 8 weeks post-trial assessment[ Pre-trial (baseline) and post-trial at 12 weeks];Update Effectiveness of implementation of MATCH Music Training Program in the management of Agitation assessed by Cohen Mansfield Agitation Inventory (CMAI) between baseline and 8 weeks post-trial assessment[ Pre-trial (baseline) and post-trial at 8 weeks]
Secondary Outcome Measures
NameTimeMethod
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