CClinicalTrials.gg
Status unknownNCT02756780Updated Apr 29, 2016

Tenovus Cancer Choirs Study: the Benefits of Singing for Those Affected by Cancer

An interventional study of Tenovus Cancer Choir in Cancer, sponsored by Royal Marsden NHS Foundation Trust. Status unknown at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-04-29.

Sponsored by Royal Marsden NHS Foundation Trust · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Apr 2016), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
420
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

'Sing With Us' choirs are an initiative established in Wales by Tenovus Cancer Care to provide social support and improve mental wellbeing amongst those affected by cancer, whether patients, carers or staff. Research has already demonstrated that these choirs can reduce depression and anxiety amongst participants and improve social support networks and quality of life as well as preliminary evidence that they can reduce levels of stress hormones and improve immune function. The aim of this study is to establish more about the psychological benefits of regular choir singing and explore whether the biological changes noted in pilot studies can be sustained over time. This could identify whether choirs have the potential to optimise health in people affected by cancer, helping to put patients in the best position to receive treatment or maintain remission and supporting those who care for someone with cancer, whether professionally or informally.

Read the detailed description

There is growing evidence that psychosocial interventions from mindfulness to yoga to the arts can reduce symptoms of depression and anxiety, increase social support networks, improve quality of life and raise perceptions of care in people affected by cancer 1,2. These positive states have, in turn, been linked with optimised immune responses including reduced stress hormones and enhanced cellular activity 1,3,4. However, despite growing numbers of music interventions for cancer care, there is little research into their psychobiological impact.

'Sing With Us' choirs are an initiative established in Wales by Tenovus Cancer Care to provide social support and improve mental wellbeing amongst those affected by cancer, whether patients, carers or staff. Research has already demonstrated that these choirs can reduce depression and anxiety amongst participants and improve social support networks and quality of life as well as preliminary evidence that they can reduce levels of stress hormones and enhance immune activity 5,6. The aim of this study is to establish more about the psychological benefits of regular choir singing and explore whether the biological changes noted in pilot studies can be sustained over time. This could identify whether choirs have the potential to optimise health in people affected by cancer, helping to put patients in the best position to receive treatment or maintain re mission and supporting those who care for someone with cancer, whether professionally or informally.

As part of this project, and in addition to the choirs already run by Tenovus Cancer Care, Tenovus will fund two choirs, one at each of the Royal Marsden sites. These will run on a weekly basis for 18 months and will consist of a session lasting 1 hour led by a professional choir leader who is a member of the Tenovus Cancer Care staff. The choirs will be open to anybody affected by cancer at the Royal Marsden Hospital or in the local area. However, there will be three cohorts of patients involved in the research running alongside the choir: cohorts A and B involving active recruitment of participants and Cohort C in which people who join the choir of their own volition but are not eligible for the first 3 cohorts will be invited to participate:

Cohort A: breast, prostate and colorectal cancer patients will be invited to join the study for a period of 12 weeks. If they are able to make the dates and times of the choir sessions they will become part of the experimental group. If they are unable to make the dates and times or live too far away but fulfil all the same criteria (including expressing an interest in singing) they will become part of the control group. Data collection for all participants will include (a) completing psychological scales which will be available in hard copy or as online versions; (b) providing saliva samples before 4 choir rehearsals: week 1, week 6 and week 12 with a three month follow-up (week 24). Experimental participants will be expected to attend as many of the first 12 choir sessions in the time period as possible but will then select whether they continue involvement in the choir for the following 12 weeks.

Cohort B: hospital staff, carers of somebody affected by cancer and bereaved carers will be invited to join the study for a period of 12 weeks. Recruitment and participation for this Cohort (including the presence of a control group) will be as in Cohort A except there will be no biological component. Participants will merely complete the online psychological questionnaires.

Cohort C: all other participants who decide to join the choirs (whether patients, carers or staff) will be invited to take part in the psychological part of the study, completing the anonymous questionnaires at weeks 0, 6, 12 and 24. This will be an uncontrolled Cohort. But it may identify additional participant groups for whom the choirs provide support.

02

Conditions studied

  • Cancer

Keywords

  • Remission
  • Carer
  • Psychological
  • Bereaved
  • Cancer
  • Breast
  • Prostate
  • Colorectal
  • Music
03

In context

Lead sponsor

Royal Marsden NHS Foundation Trust is the lead sponsor of 262 studies on the registry; 49 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

  • COHORT A: (i) Patients with stage I-III breast cancer up to 24 months post diagnosis
  • (ii) Patients with diagnosed prostate cancer on active surveillance
  • (iii) Patients with colorectal cancer stages I-III up to 24 months post diagnosis
  • COHORT B: (i) Members of staff at a hospital
  • (ii) People who care for somebody with cancer, whether formally or informally
  • (iii) People who have lost a family member or somebody they cared for to cancer in the last 3 years
  • COHORT C: anybody who is affected by cancer and has joined the choir

General exclusion Criteria:

  • Participants aged under the age of 18
  • Level of English insufficient to provide informed consent or complete the psychological questionnaires
  • Refusal to participate
  • Already engaged in a weekly group choir
  • Started a formal course of psychological therapy in the past 1 month or scheduled to start in the next 12 weeks
  • Started any new medication for anxiety or depression in the last month

Additional exclusion criteria for cohort A:

  • Currently having chemotherapy or radiotherapy or less than 90 days since last session
  • Scheduled for surgery in the next 12 weeks or less than 90 days post surgery
  • Have a current diagnosis of an additional immune condition e.g. lupus
  • Currently being treated with steroids or immunosuppressive medication
  • Participants who are pregnant
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
420 participants (estimated)

Study arms

  • Experimental
    Tenovus Cancer Choir

    Participants will be asked to attend 12 weeks of weekly choir rehearsals lasting approximately 1 hour. Following the first 12 weeks, participants will no longer be asked to attend rehearsals, but are welcome to do so. Whether or not they do and how many they attend will be measured as an outcome variable to assess whether initial 3-month involvement leads to long-term engagement.

    Other: Tenovus Cancer Choir

  • No intervention
    Control (no choir) Group

    If eligible participants are unable to make the dates and times or live too far away but fulfil all the same criteria (including expressing an interest in singing) they will become part of the control group. This will involve the same data collection as the Cancer Choir Group but participants will not sing in a weekly choir.

Interventions

  • OtherTenovus Cancer Choir

    Choir sessions will take place at both of the Royal Marsden Hospital sites on a weekly basis. Sessions typically consist of learning popular songs with messages of support. Songs are learnt without sheet music, using specially created backing tracks. These are also made available to participants at home so they can continue singing away from the sessions. No singing experience is required and the main aim of the sessions is enjoyment and meeting other people. Sessions will take place in the early evening so that participants have the option of staying to socialise afterwards.

06

What researchers measure

Primary outcomes

  1. Anxiety & Depression

    Hospital Anxiety and Depression Scale (HADS)

    Time frame: Change in anxiety and depression level at weeks 6, 12 and 24 compared to baseline

Secondary outcomes

  1. Social Support

    Social Provisions Scale (SPS)

    Time frame: Change in social provision level at weeks 6, 12 and 24 compared to baseline

  2. Wellbeing

    Warwick-Edinburgh Short Questionnaire (WEMWBS)

    Time frame: Change in wellbeing level at weeks 6, 12 and 24 compared to baseline

  3. Self-efficacy

    General Self-Efficacy scale short form (GSE-6)

    Time frame: Change in self-efficacy level at weeks 6, 12 and 24 compared to baseline

  4. Self-esteem

    Sing Item Self-Esteem Scale

    Time frame: Change in self-esteem level at weeks 6, 12 and 24 compared to baseline

  5. General Health

    Short Form 12 Health Survey (SF12)

    Time frame: Change in general health level at weeks 6, 12 and 24 compared to baseline

  6. Stress hormones

    Salivary cortisol levels

    Time frame: Change in stress hormone levels at weeks 6, 12 and 24 compared to baseline

  7. Immune proteins

    Saliva cytokines, chemokines and receptors

    Time frame: Change in immune protein levels at weeks 6, 12 and 24 compared to baseline

07

Study locations

1 of 1 sites recruiting
  • Royal Marsden Hospital NHS Foundation Trust
    London/Surrey, United Kingdom
    • Theresa Wiseman, PhD · Contact
    • Theresa Wiseman, PhD · Principal investigator
    Recruiting
08

References and documents

Publications

  • Fancourt D, Finn S, Warran K, Wiseman T. Group singing in bereavement: effects on mental health, self-efficacy, self-esteem and well-being. BMJ Support Palliat Care. 2022 Oct;12(e4):e607-e615. doi: 10.1136/bmjspcare-2018-001642. Epub 2019 Jun 26. PubMed 31243022 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 29, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02756780
Lead sponsor
Royal Marsden NHS Foundation Trust
Collaborators
London Cancer Alliance, Royal College of Music, Tenovus Cancer Care
Responsible party
Sponsor
First posted
Apr 29, 2016
Start date
Apr 2016
Primary completion
Dec 2017 (estimated)
Completion
Apr 2018 (estimated)
Last update
Apr 29, 2016

Study contacts

Daisy Fancourt, PhD
Contact
d.fancourt@imperial.ac.uk
07958 065 563
Theresa Wiseman, PhD
principal investigator · Royal Marsden NHS Foundation Trust

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Apr 2016. You cannot join it, but the record below documents what was studied.

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