WellbeingNCT07858955
Enhancing Wellbeing in Community Dwelling Seniors Through Structured Arts-Based Programmes in the Active Ageing Centres: A Mixed Method Study.
A study testing Music / Visual Arts in people with Wellbeing and Social Isolation in Older Adults, run by SingHealth Community Hospitals at 1 site in Singapore.
Trial summary
The aim of the study is to evaluate the effectiveness of structured arts-based programs conducted in the selected active ageing centres (AACs), enhancing the wellbeing of seniors. The primary objectives for this study are: 1. Read more about this study
- Who is it for?
- Ages 50 to 100 yearsHealthy volunteers can take part
- Conditions the study is for
- Wellbeing, Social Isolation in Older Adults, Social Prescribing
- What is being tested?
- Music / Visual Arts
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 239 participants
- Where
- 1 siteSingapore
- Study dates
- 20 Aug 2025to 28 Feb 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 50 to 100 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
For the structured-arts based program participants:
- Aged 50 years old and above at the time of recruitment.
- Able to converse either in English, Chinese or Malay.
- Able to complete surveys written either in English, Chinese or other languages if applicable, independently or with minimal help.
- Cognitively able to provide informed consent.
- Willing and able to participate 4-6 sessions of the structured arts-based programme and available for the duration of the study.
For the non-participants (control), they must meet all the inclusion criteria below to be recruited for the study:
- Aged 50 years old and above at the time of recruitment.
- Able to converse either in English, Chinese or Malay.
- Able to complete surveys written in either English, Chinese or other languages if applicable, independently or with minimal help.
- Do not attend any of the structured arts-based program.
- Willing and able to participate and available for the duration of the study.
- Cognitively able to provide informed consent.
Both participants and non-participants (control) of the structured-arts based program will be excluded from the recruitment are listed below:
- Going nursing home
- Palliative care
Participants of the structured-arts based program who are recruited for the focus group discussions must meet these criteria:
- Able to understand and converse either in English or Chinese.
- Able to provide informed consent.
- Attended 4-6 sessions of the structured arts-based program.
Participants who are not attending the structured-arts based program and recruited for the focus group discussions must meet these criteria:
- Able to understand and converse either in English or Chinese.
- Able to provide informed consent.
- Did not attend any of the structured arts-based program.
Artists and stage managers involved in the implementation of the structured art-based program, must meet the following criteria to be recruited for the focus group discussions:
- Has been facilitating/implementing the arts activities in the structured art-based program for at least a month.
- Aged 21 and above at time of recruitment.
- Able to understand and converse in English or Chinese.
- Able to provide informed consent.
AAC staffs and producer of the structured art-based program, recruited for individual semi-structured interviews must meet these criteria:
- Has been involved in coordinating/delivering the AAC program for at least a month.
- Aged 21 and above at time of recruitment.
- Able to understand and converse in English or Chinese.
- Able to provide informed consent.
Trial locations and contacts
1 site in 1 country.
About this study
The aim of the study is to evaluate the effectiveness of structured arts-based programs conducted in the selected active ageing centres (AACs), enhancing the wellbeing of seniors.
The primary objectives for this study are:
Read more
- To evaluate the effectiveness of the structured art-based programme on seniors' mental wellbeing using the 14- items Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS).
- To understand the perspectives of the seniors on the structured arts-based program and their behaviour and attitude change in further details after attending the program.
The secondary objectives of the study are:
To further understand the are participant satisfaction, depression and anxiety, health-related quality of life among the community dwelling seniors.
Read the detailed description
The study will be conducted at selected AACs. Using a mixed method design, integrating both quantitative and qualitative approaches to evaluate the effectiveness of structured arts-based programs for seniors by assessing the mental wellbeing of the seniors.
The quantitative approach of the study will recruit 239 subjects using purposive sampling. To evaluate the effectiveness of the structured arts program, among the 239 subjects, 170 subjects are actively engaged in the structured arts-based program conducted in the 14 AACs. 69 are non-participants (control) who are not participants in the structured arts-based program are recruited from different AACs which do not conduct the program in the AACs.
Both participants and non-participants (control) will complete questionnaires to evaluate the primary and secondary outcomes measures. This will be conducted in the AACs at their time of convenience upon obtaining informed consent. The questionnaires will be done on FormSG for data collection. To understand the mental wellbeing (primary outcome of the study), it is to measure using the 14-item Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS), a validated instrument measuring the different aspect of positive mental health. (Tennant et al., 2007)
The secondary outcomes are participant satisfaction, depression and anxiety, health-related quality of life, and social isolation. The scales used to measure these outcomes are the Patient Health Questionnaire (PHQ-9); EuroQol 5-Dimensional (EQ5D-5L); General Anxiety Disorder 7-Item (GAD-7); Patient-Reported Experience Measures (PREMS). These scales would be collected at baseline (T0), after 4 to 6 sessions of arts program (6 weeks after baseline for non-participants (control) (same amount of time as participants group) (T1), 6 months post-intervention (T2) except PREMS will be collected at T0 and T1. The questionnaire at T0 and T1 will be done face to face while questionnaire at T2 will be done face to face or through phone.
The qualitative approach of the study will recruit 30 participants and 6 non-participants (control) who did not participate in the structured art-based program into the focus group discussion. The focus group discussion will be conducted in group of 5-6 subjects in a conducive space within the AACs. Each will be guided with a topic guide which will take 60 - 90 mins face to face at ±14 days from T1 (Appendix).
In addition, eight artists and four stage managers involved in the structured art-based program will be recruited and interviewed through focus group discussions. These will be conducted in groups of 4-5 subjects, at a location and preferred time that is convenient for the participants. The focus group discussion will be guided with a topic guide which will take 60 -90 mins face to face.
Up to 14 AAC staffs and one producer of the structured arts program will be recruited for semi-structured interviews. The face-to-face semi-structured interviews will take 45-60 mins, following an interview guide for the AAC staffs and the artist FGD topic guide for the producer, at a preferred time and location of the participants.
All qualitative interviews will be audio-recorded and transcribed verbatim for analyses. All identifiable information will be mased or removed during transcription to ensure participant confidentiality.
For triangulation with the data from the surveys and qualitative interviews, the observation notes which the implementation team has been collecting for feedback to National Arts Council routinely since 5 November 2025 will be included during our data analyses. The observation form was adapted from the INNATE Framework (Warran, Burton and Fancourt, 2022) with additional focus on participants' and program implementers' behaviours, interactions (without personal identifiers) and environmental context relevant to the research questions.
- Conditions
- Wellbeing, Social Isolation in Older Adults, Social Prescribing, Anxiety Depression, Quality of Life (QOL)
- Being tested
- Music / Visual Arts
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Music / Visual ArtsBehavioural
Create soundscapes through the exploration of rhythms.
Enhance creativity and imagination through marking, tracing, drawing, and collage-making.
| Study group | Role | What they receive |
|---|---|---|
| Control | No intervention | The recruitment of non-participants (control) will be done in AACs that do not provide any of the structured arts-based program. |
| Music/ Visual Arts | Experimental | Participants will be assigned to attend four to six arts-incorporated sessions focused on music delivered by trained arts facilitators during their inpatient stay. These sessions are designed to promote emotional expression, cognitive engagement, and social interaction.
Participants attend 4-6 arts sessions focused on visual art led by trained art facilitators. These sessions aim to enhance promote emotional expression, cognitive engagement, and social interaction. Receives: Behavioral: Music / Visual Arts |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Mental Wellbeing (Warwick-Edinburgh Mental Wellbeing Scale -WEMWBS)
Mental wellbeing will be assessed using the WEMWBS, a 14-item validated scale measuring positive mental health. Higher scores indicate better wellbeing.
Measured: 1) Baseline (T0) 2) After 6 weeks post-planned intervention (T1) 3) After 6 months post planned intervention (T2)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Oct 2026
- Study start20 Aug 2025
- Primary completion14 Sep 2026
- Study completion28 Feb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for WellbeingStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Model description
- Control will have no intervention (Structured arts programme) Intervention will have either visual arts or music
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 239 participants (actual)
Sponsor and investigators
- Lead sponsor
- SingHealth Community Hospitals
- Sponsor type
- University, hospital or other
- Collaborators
- National Arts Council
- Responsible party
- Principal investigator, Lee Kheng Hock, SingHealth Community Hospitals
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07858955
- Sponsor's protocol ID
- 2025-0845-APP1
- Status last verified
- Sep 2026
- First submitted
- 24 Sep 2026
- Last updated
- 5 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: This is dependent on sponsor/funder's decision.
Study at a glance
From the registry record, last updated by the sponsor on 5 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Enhancing Wellbeing in Community Dwelling Seniors Through Structured Arts-Based Programmes in the Active Ageing Centres: A Mixed Method Study.
- ClinicalTrials.gov ID
- NCT07858955
- Acronym / sponsor ID
- 2025-0845-APP1
- Conditions
- Wellbeing, Social Isolation in Older Adults, Social Prescribing, Anxiety Depression, Quality of Life (QOL)
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 239 participants (actual)
- Lead sponsor
- SingHealth Community HospitalsUniversity, hospital or other
- Collaborators
- National Arts Council
- Study start
- 20 Aug 2025 (actual)
- Primary completion
- 14 Sep 2026 (actual)
- Study completion
- 28 Feb 2027 (estimated)
- First posted
- 5 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of the study is to evaluate the effectiveness of structured arts-based programs conducted in the selected active ageing centres (AACs), enhancing the wellbeing of seniors.
The primary objectives for this study are:
- To evaluate the effectiveness of the structured art-based programme on seniors' mental wellbeing using the 14- items Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS).
- To understand the perspectives of the seniors on the structured arts-based program and their behaviour and attitude change in further details after attending the program.
The secondary objectives of the study are:
To further understand the are participant satisfaction, depression and anxiety, health-related quality of life among the community dwelling seniors.
Detailed description
The study will be conducted at selected AACs. Using a mixed method design, integrating both quantitative and qualitative approaches to evaluate the effectiveness of structured arts-based programs for seniors by assessing the mental wellbeing of the seniors.
The quantitative approach of the study will recruit 239 subjects using purposive sampling. To evaluate the effectiveness of the structured arts program, among the 239 subjects, 170 subjects are actively engaged in the structured arts-based program conducted in the 14 AACs. 69 are non-participants (control) who are not participants in the structured arts-based program are recruited from different AACs which do not conduct the program in the AACs.
Both participants and non-participants (control) will complete questionnaires to evaluate the primary and secondary outcomes measures. This will be conducted in the AACs at their time of convenience upon obtaining informed consent. The questionnaires will be done on FormSG for data collection. To understand the mental wellbeing (primary outcome of the study), it is to measure using the 14-item Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS), a validated instrument measuring the different aspect of positive mental health. (Tennant et al., 2007)
The secondary outcomes are participant satisfaction, depression and anxiety, health-related quality of life, and social isolation. The scales used to measure these outcomes are the Patient Health Questionnaire (PHQ-9); EuroQol 5-Dimensional (EQ5D-5L); General Anxiety Disorder 7-Item (GAD-7); Patient-Reported Experience Measures (PREMS). These scales would be collected at baseline (T0), after 4 to 6 sessions of arts program (6 weeks after baseline for non-participants (control) (same amount of time as participants group) (T1), 6 months post-intervention (T2) except PREMS will be collected at T0 and T1. The questionnaire at T0 and T1 will be done face to face while questionnaire at T2 will be done face to face or through phone.
The qualitative approach of the study will recruit 30 participants and 6 non-participants (control) who did not participate in the structured art-based program into the focus group discussion. The focus group discussion will be conducted in group of 5-6 subjects in a conducive space within the AACs. Each will be guided with a topic guide which will take 60 - 90 mins face to face at ±14 days from T1 (Appendix).
In addition, eight artists and four stage managers involved in the structured art-based program will be recruited and interviewed through focus group discussions. These will be conducted in groups of 4-5 subjects, at a location and preferred time that is convenient for the participants. The focus group discussion will be guided with a topic guide which will take 60 -90 mins face to face.
Up to 14 AAC staffs and one producer of the structured arts program will be recruited for semi-structured interviews. The face-to-face semi-structured interviews will take 45-60 mins, following an interview guide for the AAC staffs and the artist FGD topic guide for the producer, at a preferred time and location of the participants.
All qualitative interviews will be audio-recorded and transcribed verbatim for analyses. All identifiable information will be mased or removed during transcription to ensure participant confidentiality.
For triangulation with the data from the surveys and qualitative interviews, the observation notes which the implementation team has been collecting for feedback to National Arts Council routinely since 5 November 2025 will be included during our data analyses. The observation form was adapted from the INNATE Framework (Warran, Burton and Fancourt, 2022) with additional focus on participants' and program implementers' behaviours, interactions (without personal identifiers) and environmental context relevant to the research questions.
Study design
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
- Model description
- Control will have no intervention (Structured arts programme) Intervention will have either visual arts or music
| Arm | Type | Receives |
|---|---|---|
| Control | No intervention | –The recruitment of non-participants (control) will be done in AACs that do not provide any of the structured arts-based program. |
| Music/ Visual Arts | Experimental | Behavioral: Music / Visual ArtsParticipants will be assigned to attend four to six arts-incorporated sessions focused on music delivered by trained arts facilitators during their inpatient stay. These sessions are designed to promote emotional expression, cognitive engagement, and social interaction. Participants attend 4-6 arts sessions focused on visual art led by trained art facilitators. These sessions aim to enhance promote emotional expression, cognitive engagement, and social interaction. |
Who may qualify
- Ages
- 50 to 100 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Music / Visual ArtsCreate soundscapes through the exploration of rhythms. Enhance creativity and imagination through marking, tracing, drawing, and collage-making. | Behavioural | Music/ Visual Arts |
Primary outcome
Change in Mental Wellbeing (Warwick-Edinburgh Mental Wellbeing Scale -WEMWBS)
Time frame: 1) Baseline (T0) 2) After 6 weeks post-planned intervention (T1) 3) After 6 months post planned intervention (T2)
Mental wellbeing will be assessed using the WEMWBS, a 14-item validated scale measuring positive mental health. Higher scores indicate better wellbeing.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Oct 2026.
- Individual participant dataSharing planned: Undecided. This is dependent on sponsor/funder's decision.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Music / Visual Arts in people with Wellbeing and Social Isolation in Older Adults, run by SingHealth Community Hospitals at 1 site in Singapore.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 5 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Singapore. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Mental Wellbeing (Warwick-Edinburgh Mental Wellbeing Scale -WEMWBS) (time frame: 1) Baseline (T0) 2) After 6 weeks post-planned intervention (T1) 3) After 6 months post planned intervention (T2)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Oct 2026.