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Support in Sound: Music Therapy for People Living With Dementia and Companions in Rural Communities

3 luglio 2026 aggiornato da: Anglia Ruskin University

The Support in Sound Music Therapy Research Project for People Living With Dementia and Companions in Rural Communities

The goal of this single-arm feasibility study is to learn whether group music therapy is feasible in a rural area for people living with dementia and their companions. The main questions are:

  1. Is a group music therapy intervention feasible in a rural community setting? 1a. Are there preliminary changes in health and well-being outcomes following participation in a 10-week community music therapy group?
  2. What were participants' experiences and preferences regarding the different components of the music therapy programme?
  3. What is the role of peer support in participants' experiences of a community music therapy intervention?

Participants living with dementia and their companions will be asked to take part in 10-weeks of music therapy in the community. Before and after each music therapy session, they will be asked to answer an easy-read satisfaction survey to gather information on the 'in the moment' experiences of music therapy.

Participants will also be asked to complete surveys on quality of life, loneliness, depression and well-being on three occasions:

  • Before music therapy starts
  • During week 5 of music therapy
  • After music therapy

After music therapy, participants will also be asked to

  • Complete a survey about their experiences of different parts of the music therapy programme
  • Take part in an individual feasibility interview
  • Take part in an interview exploring the role of peer support within the music therapy groups

If a person does not have the capacity to answer any questions, their companion will be asked to provide the information on behalf of the individual living with dementia.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Descrizione dettagliata

Support in Sound is a 14-week research project for people living with dementia and their carers in Tarporley and the surrounding villages. The project explores how community-based group music therapy may support quality of life, social connection, depression and well-being for participants.

Research suggests that music therapy can have positive emotional and social benefits for people living with dementia. A study found that group music therapy significantly reduced anxiety and depression compared to usual care, with improvements still present three months later, suggesting possible longer-term mental health benefits. A Cochrane review also found that music-based therapeutic interventions may improve social behaviour, depressive symptoms, and overall behavioural symptoms in people with dementia. In addition, music therapy may help facilitate positive emotions and strengthen connections with significant others.

However, less is known about the practicalities, accessibility, and acceptability of delivering group music therapy in rural communities. People living in rural areas may have fewer opportunities to access support groups, wellbeing activities and meet with peers than those living in towns and cities. There is also limited research exploring the role of peer support and shared social experiences within group music therapy for people living with dementia and their carers.

Participants will be recruited from Tarporley and the surrounding villages in line with supporting the health and well-being of local residents living with dementia and their companions in the community. Recruitment posters will be advertised around the village and circulated with care groups in the area. Consent will be obtained from caregivers and individuals living with dementia if they have capacity to do so. Where a person does not have capacity, a consultee will complete a declaration form on behalf of the person living with dementia. Demographic data will be collected before the study commences.

The project consists of 2 weeks for baseline data collection, 10-weeks of group music therapy including data collection during week 5 and 2 weeks of data collection at the end of the study.

The music therapy will be delivered by a HCPC registered music therapist with experience of working with people living with dementia. The sessions will include singing, listening to music, playing with instruments and using music to enable social engagement. Sessions will include an opportunity for peers to socialise over tea, coffee and cake before and after each music therapy session. The team aims to recruit between 6 - 7 dyads.

Feasibility data will be collected to understand the practicality and acceptability of the study using the following data:

  • Recruitment rates: Monitoring the number of people recruited
  • Retention data: Monitoring the number of people who completed the study
  • Adherence rates: Marking an online register each time a person attends a session
  • Collecting current mood before and after each music therapy session and satisfaction at the end of each session
  • An end of study feasibility interview with participants focused on the implementation, mechanisms of impact and context.

The potential preliminary changes in health and well-being of both persons living with dementia and their companions will be measured using the following data:

  • Quality of life - DEMQOL and DEMQOL Proxy
  • Loneliness - UCL Loneliness 3-point scale
  • Depression - Short Geriatric Depression Scale
  • Well-being - Short Warwick-Edinburgh Mental Wellbeing Scale

All participants will be asked to complete each of the outcome measures before music therapy, during week 5 of music therapy and at the end of music therapy to measure potential changes during the course of participating in music therapy.

Additional information will be requested to:

  1. Learn about the perceived satisfaction and value of each of the components of the music therapy programme. This data will be conducted using a survey designed on Microsoft Forms
  2. Learn about the potential role of peer support within the music therapy programme using a semi-structured interview guide.

Descriptive data will be analysed and there will be a repeated measures analysis. Interview data will be analysed qualitatively.

Tipo di studio

Interventistico

Iscrizione (Stimato)

14

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Kiera Kenny, PhD
  • Numero di telefono: +447979154869
  • Email: kk79@aru.ac.uk

Luoghi di studio

      • Chester, Regno Unito
        • Tarporley Community Centre
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • One person must have a clinical diagnosis of dementia and be accompanied by a companion
  • Participants must be able to attend the 10-week programme, recognising that unavoidable absences (e.g., illness or unforeseen personal circumstances) may occur
  • Be willing to provide data on health and well-being and take part in interviews.
  • Be able to speak and understand the English language

Exclusion Criteria:

  • Individuals, as dyads are the participants being recruited
  • Dyads were neither person has a clinical diagnosis of dementia
  • Are unavailable to generally commit to the research programme including music therapy sessions
  • Are unable to speak or understand the English language

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Terapia di supporto
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Music therapy group
Group music therapy will be delivered to participants for 10-weeks.
Group music therapy will be held in the local community of Tarporley for 10 weeks. The music therapy will be delivered by a HCPC registered music therapist with experience of working with people living with dementia. Each session will be held for 1.5 hours: consisting of 1 hour of music therapy and the remaining time available for participants to have tea, coffee and cake providing an opportunity to talk and socialise. All participants will be provided with a name label before each session. The one hour of weekly music therapy will consist of singing, music listening, playing with instruments and interactive music making opportunities.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Acceptability and practicality of the study
Lasso di tempo: From enrolment to the end of the 14-week research programme
The following feasibility measures will be collected to assess the acceptability and practicality of the study: number of participants who were recruited, adhered and retained to the study. Numerical levels of satisfaction throughout the duration of the study and qualitative details on feasibility from participants.
From enrolment to the end of the 14-week research programme

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Dementia quality of life measure: DEMQOL
Lasso di tempo: Up to two weeks before the music therapy programme starts, again at week 5 and up to two weeks after music therapy programme.

Quality of life of participants living with dementia will be measured using the DEMQOL questionnaire or the DEMQOL proxy questionnaire completed by their companion if a person does not have capacity to answer for themselves.

Scoring:

DEMQOL: (minimum score) 28-112 (maximum score); higher score = better quality of life.

DEMQOL-Proxy: (minimum score) 31-124 (maximum score); higher =better quality of life as rated by a caregiver/proxy).

Up to two weeks before the music therapy programme starts, again at week 5 and up to two weeks after music therapy programme.
UCLA 3-item Loneliness Scale
Lasso di tempo: Up to two weeks before the music therapy programme starts, again at week 5 and up to two weeks after music therapy programme.

Loneliness will be measured of both participants living with dementia and their companions using the UCLA 3-item Loneliness Scale. If a person does not have capacity, their companion will complete this on behalf of the person living with dementia.

Scoring:

3 (minimum score) - 9 (maximum score) with higher scores indicating greater loneliness.

Up to two weeks before the music therapy programme starts, again at week 5 and up to two weeks after music therapy programme.
Short Geriatric Depression Scale (GDS 15)
Lasso di tempo: Up to two weeks before the music therapy programme starts, again at week 5 and up to two weeks after music therapy programme.

Depression levels will be measured using the Short Geriatric Depression Scale for both individuals living with dementia and their companions for those over 65 years of age. If a person does not have capacity, their companion will complete this on behalf of the person living with dementia.

Scoring:

0 (minimum score) - 15 (maximum score) with higher scores indicating worse depressive symptoms

Up to two weeks before the music therapy programme starts, again at week 5 and up to two weeks after music therapy programme.
Short Warwick-Edinburgh Mental Wellbeing Scale
Lasso di tempo: Up to two weeks before the music therapy programme starts, again at week 5 and up to two weeks after music therapy programme.

Well-being will be measured using the Short Warwick-Edinburgh Mental Wellbeing Scale for both person living with dementia and their companions. If a person does not have capacity, their companion will complete this on behalf of the person living with dementia.

Scoring:

7 (minimum score) - 35 (maximum score) with higher scores indicating better well-being.

Up to two weeks before the music therapy programme starts, again at week 5 and up to two weeks after music therapy programme.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

3 agosto 2026

Completamento primario (Stimato)

16 novembre 2026

Completamento dello studio (Stimato)

30 novembre 2026

Date di iscrizione allo studio

Primo inviato

25 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

3 luglio 2026

Primo Inserito (Effettivo)

9 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 luglio 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Descrizione del piano IPD

All data collected including demographics, participants and information sheets, feasibility data, questionnaire data and interview data will be shared within the research team.

Periodo di condivisione IPD

In the first month of the study up until the research has been published ~ 2 years.

Criteri di accesso alla condivisione IPD

The research team will be able to access all IPD throughout the study. The data will be stored on a password protected OneDrive folder. The folder will be shared with the research team only and they will have the password to access the folder. There will be one Excel sheet with participants names and demographic information, where a unique ID code will be assigned to each participant. All survey and interview data will be labelled with the participant's unique code rather their name.

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA
  • ICF
  • RSI

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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