Managing the Needs of Care Home Residents With Dementia Through a Music Therapy Intervention

June 10, 2026 updated by: Anglia Ruskin University

Managing the Needs of Care Home Residents Through a Music Therapy Intervention: A Non-randomised Feasibility Trial

The purpose of this study is to implement and evaluate a music therapy intervention in care homes. The primary aim is to assess whether implementing the intervention will have an impact on unmet in care homes for people living with dementia. Researchers will also examine the feasibility of a music therapy programme in care homes and its effects on care staff and residents with cognitive impairment. Care home staff will also receive training with music therapists via video communications to help staff use music therapy techniques to support people living with dementia.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This project aims to evaluate the feasibility and effectiveness of a 12-week music therapy programme in care homes for residents with cognitive impairment/dementia and care home staff using a non-randomised control design. Music therapy is widely recognised as beneficial for people living with dementia. However, little is known about its overall impact on quality of care in care homes.

Research questions:

  1. Can a music therapy intervention improve quality of care in care homes by supporting residents' needs?
  2. What are the effects of music therapy on residents with cognitive impairment and care home staff?
  3. Is the implementation of a music therapy programme feasible in care homes?
  4. For the treatment of symptoms of dementia, is music therapy a cost-effective treatment in care homes?

Intervention:

The team will invite a total of 84 participants from 12 care homes located across the North and South of England to take part in the study. This includes 48 participants with cognitive impairment/dementia and 36 care home staff. The team will recruit a qualified music therapist in each region to work within the care home to deliver the music therapy intervention.

Residents with cognitive impairment/dementia will be invited to receive twenty 30-minute individual music therapy sessions across 12 weeks. The therapy will be video recorded for training purposes. Data will be collected about residents to learn about their needs and any health and wellbeing symptoms. This will help inform music therapists about each individuals' specific needs so that they can tailor a suitable treatment approach. They will enable a meaningful, engaging therapeutic relationship to improve the health and wellbeing of residents. The sessions will focus on targeting specific behavioural and psychological symptoms of dementia by providing cognitive stimulation, communicative support and social connectedness.

Within the 12-week programme, care home staff participants will be invited to collectively receive music therapy training on four occasions during week 3, 6, 9 and 12. Each music therapist will demonstrate significant moments of their sessions to staff via short video clips from a music therapy session. They will provide clinical explanations to staff about the techniques they have used and why they are effective for the individuals with cognitive impairment.

Data collection:

The team will be collecting a range of qualitative and quantitative data. The researchers will use an integrated evaluative approach focussing on clinical and organisational outcomes to examine the research questions. As part of the non-randomised control design, six of the care homes will be in the intervention group and receive the music therapy programme. There will be 42 participants in this group (24 with cognitive impairment, 18 care home staff). The remaining six care homes will form the control group and receive treatment as usual. Baseline and post 12-week data will be collected from all homes to compare differences between groups. Within group data will also be compared from the intervention homes.

Once all of the data has been collected from the control group care homes, they will then go on to receive the music therapy programme with the same amount and ratio of participants.

Implications:

The study has the potential to improve the lives of care home residents living with cognitive impairment/dementia. It also has the potential to improve the work life of care home staff and generate better quality of care. Staff will be provided with the tools and understanding of music therapy techniques, so that the potential effects can be sustainable. Standardised protocols are needed to learn about how researchers and practitioners can work with the social care sector to implement an effective music therapy programme. The evaluation of this study will inform this sector about the feasibility and effectiveness of music therapy care in care homes. The study findings will provide valuable insights into how to transform the social care sector through psychosocial, non-pharmacological intervention at micro and macro level.

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Study Type

Interventional

Enrollment (Actual)

76

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Doncaster, United Kingdom, DN7 6JQ
        • Hatfield House
      • Leeds, United Kingdom, LS21 1RJ
        • Simon Marks Court
      • Leeds, United Kingdom, LS9 6BT
        • Oak Tree Lodge
      • Newquay, United Kingdom, TR7 1JG
        • Kimberly Court
      • Otley, United Kingdom, LS21 1RJ
        • Wharfside
      • Saltash, United Kingdom, PL12 6DJ
        • St Anne's
      • Sheffield, United Kingdom, S11 9AB
        • Prior Bank
      • Sheffield, United Kingdom, S5 8TT
        • Herries Lodge
    • Surrey
      • Banstead, Surrey, United Kingdom, SM7 2BQ
        • Ridgemount
      • London, Surrey, United Kingdom, RH9 8BD
        • Oakleigh, Godstone
      • London, Surrey, United Kingdom, SM7 2BQ
        • Greenacres, Banstead

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 105 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria

The proposed inclusion criteria for care home residents are as follows:

  • Participants must be aged 50+ years
  • Participants will be a resident of one of the 12 care homes taking part
  • For each participant, there must be clinical evidence of cognitive impairment. This will be determined by a score of 24 or under on the SMMSE
  • Each participant must display at least one behavioural/psychological symptom of dementia. This will be determined by a score of 4 or higher on the NPI-NH.

The proposed inclusion criteria for care home staff are as follows:

  • Participants must be aged 18+ years
  • Participants must have worked in the care home for at least 3 months
  • Participants will be required to have in-depth knowledge of the resident participant(s). This will be determined through communications with home managers to ensure each staff member is paired with a resident they provide regular care for.

Exclusion Criteria

Exclusion criteria for care home residents:

- Participants who's health appears to be at risk which raises the concerns of their sustained involvement with the study. This would be evident from a health assessment from a general practitioner. Given that this is a music therapy study, this could also include people with a hearing impairment.

Exclusion criteria for care home staff:

- Staff who cannot adequately answer on behalf of the residents due to lack of knowledge of the residents.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Music therapy intervention
Music therapy
Individual music therapy sessions across 12-weeks with people with cognitive impairment/dementia. Music therapy training for care home staff at four time points across 12-weeks.
No Intervention: Control group - standard care
Standard care for residents with cognitive impairment. Staff will not receive music therapy training.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Camberwell Assessment of Needs in the Elderly - CANE
Time Frame: 15 minutes
For people with cognitive impairment - to measure the quality of care in care homes by assessing individual needs. This measure examines met and unmet needs in older people in 24 areas from self-care to communicative abilities. 1 = a met need, 2 = an unmet need. Met needs and unmet needs are totalled. A higher score indicates a higher number of needs.
15 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Standardised Mini Mental State Examination - SMMSE
Time Frame: 15 minutes
For people with cognitive impairment - a standardised assessment to test cognitive function of residents in care homes. This version will factor in participants with various impairments such as visual and motor issues. Scores are between 0 and 30. Lower scores indicate lower cognitive function.
15 minutes
Neuropsychiatric Inventory Nursing Homes - NPI-NH
Time Frame: 12 minutes
Care home staff will be interviewed to measure the neuropsychiatric symptoms of people with dementia in care homes. Data is collected about a range of symptoms from A-J including delusions, anxiety, aberrant motor behaviours, disinhibition. If a symptom is present, the frequency is scored from 1 (rarely) - 4 (very often), the severity is scored from 1 (mild) - 3 (severe). Frequency x severity provides an NPI score for each present symptom which is totalled. Occupational disruptiveness is also scored for a present symptom from 1 (not at all) - 5 (very severe). Occupational disruptiveness scores are totalled to provide an overall score.
12 minutes
EuroQoL - EQ-5D-5L - self completion
Time Frame: 5 minutes
Residents will respond to which level they perceive in five domains (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) with level 1 (no problem) to level 5 (extremely). Each number representing a level will develop a code (e.g. 11111 would indicate no problems in health related quality of life). These scores can then be formulated into an index value.
5 minutes
EuroQoL - EQ-5D-5L - proxy
Time Frame: 5 minutes
The same measure as above to assess proxy health related quality of life. This will be completed by a care staff member and scoring will be as above.
5 minutes
Barthel Index (BI)
Time Frame: 10 minutes
A survey link will be sent out to care staff to measure the perceived functional abilities of the individuals with dementia such as feeding, bathing etc. Care staff will be asked the questions to provide their opinions on one domain (activities of daily living) with 10 items. Scores range between 0 and 100. A higher score indicates a better outcome with higher levels of independence.
10 minutes
Job Satisfaction Index (JSI)
Time Frame: 10 minutes
A survey link will be sent out to care staff to measure job satisfaction based on 18 statements using five categories from strongly agree - strongly disagree.
10 minutes
Maslach Burnout Inventory - Human services (MBI-HSS)
Time Frame: 10 minutes
A survey link will be sent out to care staff to measure burnout. Questions are based around three areas: emotional exhaustion, depersonalisation and personal accomplishments. There are a total of 22 questions related to how one feels in their job, on a scale from 0 (never) - 6 (every day). Average scores are calculated.
10 minutes
Qualitative semi-structured Interviews
Time Frame: 10 - 20 minutes
A semi-structured interview with care staff will be carried out at baseline in both groups until data saturation is met. This interview consists of questions about the concept of quality of care and job satisfaction. Another interview will be carried out with all care staff participants in the intervention group at the end of the music therapy treatment to evaluate the music therapy process.
10 - 20 minutes
Client Service Receipt Inventory (CSRI Dementia)
Time Frame: 15 minutes
A measure of the cost effectiveness of the music therapy in care homes. This instrument collects information about service usage of residents, medication usage and overall care home costs.
15 minutes
Total number of staff at the care home
Time Frame: 2 minutes
The total number of staff at each care home is collected in both groups, pre and post to examine staff retention and turnover.
2 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Helen Odell-Miller, PhD, Anglia Ruskin University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 4, 2022

Primary Completion (Actual)

April 30, 2024

Study Completion (Actual)

May 13, 2024

Study Registration Dates

First Submitted

December 15, 2021

First Submitted That Met QC Criteria

December 15, 2021

First Posted (Actual)

January 4, 2022

Study Record Updates

Last Update Posted (Actual)

June 12, 2026

Last Update Submitted That Met QC Criteria

June 10, 2026

Last Verified

January 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Data will be anonymous

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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