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Personalized Music Therapy and Agitation in Dementia

Assessing the Effects of a Personalized Music Therapy With Headphones on Agitation in Patients With Dementia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02147652
Enrollment
60
Registered
2014-05-28
Start date
2014-10-14
Completion date
2020-06-30
Last updated
2019-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's Disease, Vascular Dementia

Keywords

moderate dementia, severe dementia, Alzheimer's disease, Vascular dementia, agitation, personalized music therapy

Brief summary

Symptoms of agitation include abuse or aggressive behaviour toward self or others, appropriate behaviour performed with inappropriate frequency, or behaviours that are inappropriate according to social standards. In the later stages of dementia agitation can contribute significantly to patient distress and caregiver stress, and has been associated with poor quality of life. Previous research studies have shown some evidence that personalized music played in daily care situations reduces agitation. The purpose of this study is to evaluate the effects of personalized music therapy via headphones on agitation during hygiene care (grooming). This study will involve 60 in-patients of the Geriatric Psychiatry ward of Toronto Rehabilitation Institute. The study would take place over the span of 2 weeks and would involve listening to personalized and either non-personalized or no music during daily hygiene care (grooming). Enrolment is completely voluntary and all personal data obtained will remain confidential.

Interventions

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of dementia with possible or probable cause of Alzheimer's disease, Vascular disease, mixed dementia; * moderate stage of dementia, a score of \<20 on MMSE; * Age 60 to 90 inclusive; * Preserved hearing (hearing aids are permissible); * Pittsburgh agitation scale score of ≥ 3 on at least on 3 occasions over a period of 5 days.

Exclusion criteria

* auditory deficits requiring correction beyond hearing aids. * no substitute decision maker available to indicate music preference and patient unable to answer for themselves. * recent acute event eg. MI, fractures, or major infection (not UTI) * patients receiving standing orders of medication for personal care

Design outcomes

Primary

MeasureTime frameDescription
Changes in agitation2 weeksChanges in agitation as measured by the Pittsburgh agitation questionnaire and as needed psychotropic medications for agitation required during hygiene care will be quantitatively assessed. Statistical analyses will be performed to compare levels of agitation and use of as needed psychotropic medications for agitation with personalized music therapy with headphones and non-personalized music intervention or usual care.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026