ArtNCT05945589
The Singapore Art-Health Study
A study testing Singapore A-Health Intervention in people with Art and Wellness, Psychological, run by Nanyang Technological University at 1 site in Singapore.
Trial summary
The goal of the Singapore Art-Health RCT is to examine the effect of a standardized 12-week museum -based participatory art program on health condition, well-being, and quality of life in older community dweller, one that adheres to the Montreal Art-Health framework with culturally specific modifications that are… Read more about this study
- Who is it for?
- Ages 60 to 99 yearsHealthy volunteers can take part
- Conditions the study is for
- Art, Wellness, Psychological, Frailty
- What is being tested?
- Singapore A-Health Intervention
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 112 participants
- Where
- 1 siteSingapore
- Study dates
- 2 Mar 2021to 31 Dec 2021
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 60 to 99 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- individuals above the age of 60,
- fluent in English
- able to access the internet to complete the online psychometric assessments
Who cannot join
- unable to provide informed consent
- diagnosed with mental health conditions
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effects of Participatory Art-Based Activity On Health of Older Community-Dwellers: The Singapore Art-Health Randomized Control Trial Study
The goal of the Singapore Art-Health RCT is to examine the effect of a standardized 12-week museum -based participatory art program on health condition, well-being, and quality of life in older community dweller, one that adheres to the Montreal Art-Health framework with culturally specific modifications that are fitting to the local Singaporean context.
Participants will be randomized into an intervention group of a passive control group. Participants in the intervention group will be invited to participate in the 12-week Singapore Art-Health Intervention held at the National Gallery Singapore. All participants will be invited to complete four online psychometric assessments. Participants in the intervention group will be invited to completed an additional post-intervention survey and a feasibility focus group.
Read the detailed description
Background: Population aging continues to be global health challenge. The prevalence of longstanding age-related conditions such as worsening physical, social, and mental health is expected to increase exponentially with a rapidly ageing population. The practice of participatory art in various settings has been found to be effective in the promotion, prevention and management of health and wellbeing conditions across the life span. However, its effect on health condition among the older population, particularly in the Asian context remains to be investigated. In Montreal, findings from a pilot study provided strong evidence to show that a 12-week, standardized "Art-Health" participatory art program had multidimensional positive effects on the health outcomes of older community dwelling participants including improvements in wellbeing, quality of life, and frail condition.
Current Proposal: The current research will adopt and modify the Montreal Art-Health participatory art framework with local cultural specificity (i.e. The Singapore Art-Health Intervention), and tests its effectiveness in healthy and wellness promotion among a sample of Singaporean older adults via a randomized control trial.
Research Design: The study adopts a participatory action research paradigm and a single-site, open-label Randomized Control Trial (RCT) design to develop and examine the effect of a standardized 12-week museum-based participatory art activity on health condition, wellbeing, and quality of life in older community dwellers.
Sampling and Randomization: Allowing for an attrition rate of 5% at follow-up, a target sample of 110 provides 90% power to detect an effect size of 0.55 (based on the results of the pilot study) between the intervention group and the control group at 5% level of significance (two-tailed test). Participants will be randomized into an intervention group of a passive control group. Participants in the intervention group will be invited to participate in the 12-week Singapore A-Health Intervention held at the National Gallery Singapore.
Intervention Design: The Singapore Art-Health Intervention will span 12 weeks, with each weekly session lasting for two hours. The program is designed to impart basic art appreciation skill (formal analysis in art) and art making techniques to participants through engagement with the collection at the museum.
Outcome measures and Data Analysis: All participants will be invited to complete four online psychometric assessments. Participants in the intervention group will be invited to completed an additional post-intervention survey and a feasibility focus group. For the quantitative data, between and within comparisons of outcomes will be conducted by mixed model analysis of variance (ANOVA), repeated measures ANOVA, and pairwise t-tests with Bonferroni correction. The focus group discussions will be analyzed using thematic analysis with a grounded theory approach to provide insights to the participant's experience and impact of the Singapore Art-Health Intervention.
Importance of Research: The current research will develop and test the effectiveness of a culturally-specific Art-Health participatory art program on health and wellness promotion among a sample of Singaporean older adults. Working collaboratively with the National Gallery Singapore in program development and implementation will serve to ensure program sustainability upon research completion. This collaboration will also foster practice and knowledge transfer to accelerate creative ageing in the local society. Moreover, the findings will contribute to an international RCT for evaluating a standardized participatory art framework to address the impact of population ageing. It will be a potential breakthrough in the development of an efficient art and museum program for older adults locally and internationally.
- Conditions
- Art, Wellness, Psychological, Frailty, Quality of Life
- Being tested
- Singapore A-Health Intervention
- Keywords
- Art, Museum, Quality of Life, Frailty
- Medical subject headings
- Psychological Well-Being, Frailty
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Singapore A-Health InterventionBehavioural
The Singapore A-Health Intervention spanned 12 weeks, with each weekly session lasting for two hours. The program is structured around three thematic domains of the past, present, and future. In each thematic domain consisting of four weeks, participants were tasked with creating an artwork related to the theme and incorporating the learned art techniques. The structure of each thematic domain follows the same structure: the first week involved a 45-minute docent-led gallery tour on three selected pieces of artworks, followed by a 75-minute artist-led brainstorming session where participants were introduced to the techniques and discuss ideas on the artwork to be created. The subsequent three sessions involved further guidance from the artist and a scaffolded delivery of art techniques for participants to incorporate their learning to their artwork. At the end of each domain, there was a showcase where participants present their artwork.
| Study group | Role | What they receive |
|---|---|---|
| Singapore A-Health Group | Experimental | A 12-week professionally led participatory art program at the gallery with each week comprising one 2-hour art session, totaling 24 hours of museum tours and participatory art activities. Receives: Behavioral: Singapore A-Health Intervention |
| Control Group | No intervention | No art-based activities offered and advised not to participate in concurrent health and art-based interventions during the 12-week research period. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Quality of Life (EQ5D)
Quality of life will be assessed by EuroQol-5D (EQ5D) which comprised of two parts: (1) 5-item scale on mobility, self-care, daily activities, pain, and depressive symptoms, (2) a visual analog scale of the participant's perceived health ranging from 0 (worst health) to 100 (best health one can imagine)
Measured: Baseline
Change in Quality of Life (EQ5D)
Quality of life will be assessed by EuroQol-5D (EQ5D) which comprised of two parts: (1) 5-item scale on mobility, self-care, daily activities, pain, and depressive symptoms, (2) a visual analog scale of the participant's perceived health ranging from 0 (worst health) to 100 (best health one can imagine)
Measured: 5-week follow-up
Change in Quality of Life (EQ5D)
Quality of life will be assessed by EuroQol-5D (EQ5D) which comprised of two parts: (1) 5-item scale on mobility, self-care, daily activities, pain, and depressive symptoms, (2) a visual analog scale of the participant's perceived health ranging from 0 (worst health) to 100 (best health one can imagine)
Measured: 9-week follow-up
Change in Quality of Life (EQ5D)
Quality of life will be assessed by EuroQol-5D (EQ5D) which comprised of two parts: (1) 5-item scale on mobility, self-care, daily activities, pain, and depressive symptoms, (2) a visual analog scale of the participant's perceived health ranging from 0 (worst health) to 100 (best health one can imagine)
Measured: 12-week follow-up
Mental Wellbeing (WEMWBS)
Mental Wellbeing will be assessed by Warwick-Edinburgh Mental Wellbeing Scales (WEMWBS), a 14-item scale assessing various domains of wellbeing.
Measured: Baseline
Change in Mental Wellbeing (WEMWBS)
Mental Wellbeing will be assessed by Warwick-Edinburgh Mental Wellbeing Scales (WEMWBS), a 14-item scale assessing various domains of wellbeing.
Measured: 5-week follow-up
Change in Mental Wellbeing (WEMWBS)
Mental Wellbeing will be assessed by Warwick-Edinburgh Mental Wellbeing Scales (WEMWBS), a 14-item scale assessing various domains of wellbeing.
Measured: 9-week follow-up
Change in Mental Wellbeing (WEMWBS)
Mental Wellbeing will be assessed by Warwick-Edinburgh Mental Wellbeing Scales (WEMWBS), a 14-item scale assessing various domains of wellbeing.
Measured: 12-week follow-up
Frailty (CESAM)
Frailty will be assessed by the Centre of Excellence on Longevity Self-administered Questionnaire (CESAM). It is a 20-item scale assessing multiple aspects of health such as drug intake, memory complaints, health service utilization, and activities of daily living.
Measured: Baseline
Change in Frailty (CESAM)
Frailty will be assessed by the Centre of Excellence on Longevity Self-administered Questionnaire (CESAM). It is a 20-item scale assessing multiple aspects of health such as drug intake, memory complaints, health service utilization, and activities of daily living.
Measured: 5-week follow-up
Change in Frailty (CESAM)
Frailty will be assessed by the Centre of Excellence on Longevity Self-administered Questionnaire (CESAM). It is a 20-item scale assessing multiple aspects of health such as drug intake, memory complaints, health service utilization, and activities of daily living.
Measured: 9-week follow-up
Change in Frailty (CESAM)
Frailty will be assessed by the Centre of Excellence on Longevity Self-administered Questionnaire (CESAM). It is a 20-item scale assessing multiple aspects of health such as drug intake, memory complaints, health service utilization, and activities of daily living.
Measured: 12-week follow-up
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Jul 2023
- Study start2 Mar 2021
- Primary completion30 Nov 2021
- Study completion31 Dec 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for ArtStudies 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
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Intervention group participants will be invited to engaged in a 12-week participatory art program at the gallery. Participants in the control condition will not offered any art-based activities. All participants were advised not to participate in concurrent health art-based interventions during the research period.
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 112 participants (actual)
Sponsor and investigators
- Lead sponsor
- Nanyang Technological University
- Sponsor type
- University, hospital or other
- Collaborators
- National Gallery Singapore, Singapore, Sheffield Hallam University, Université de Montréal
- Responsible party
- Principal investigator, Andy Hau Yan Ho, PhD, EdD, Nanyang Technological University
- Investigators
- Andy HY Ho, PhD, EdD, Principal investigator, Nanyang Technological University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05945589
- Sponsor's protocol ID
- IRB-2020-02-005
- Status last verified
- Jul 2023
- First submitted
- 5 Jul 2023
- Last updated
- 14 Jul 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: There are currently no plans o make individual participant data (IPD) available to other researchers.
Publications
Beauchet O, Cooper-Brown LA, Hayashi Y, Deveault M, Ho AHY, Launay CP. Health benefits of "Thursdays at the Montreal Museum of Fine Arts": Results of a randomized clinical trial. Maturitas. 2021 Nov;153:26-32. doi: 10.1016/j.maturitas.2021.07.013. Epub 2021 Jul 31.
PubMed 34654525Beauchet O, Bastien T, Mittelman M, Hayashi Y, Hau Yan Ho A. Participatory art-based activity, community-dwelling older adults and changes in health condition: Results from a pre-post intervention, single-arm, prospective and longitudinal study. Maturitas. 2020 Apr;134:8-14. doi: 10.1016/j.maturitas.2020.01.006. Epub 2020 Jan 13.
PubMed 32143777Ho AHY, Ma SHX, Tan MKB, Bajpai R, Goh SSN, Yeo G, Teng A, Yang Y, Galery K, Beauchet O. Effects of participatory 'A'rt-Based Activity On 'Health' of Older Community-Dwellers: results from a randomized control trial of the Singapore A-Health Intervention. Front Med (Lausanne). 2023 Dec 21;10:1238562. doi: 10.3389/fmed.2023.1238562. eCollection 2023.
PubMed 38188333
Study at a glance
From the registry record, last updated by the sponsor on 14 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Participatory Art-Based Activity On Health of Older Community-Dwellers: The Singapore Art-Health Randomized Control Trial Study
- ClinicalTrials.gov ID
- NCT05945589
- Acronym / sponsor ID
- IRB-2020-02-005
- Conditions
- Art, Wellness, Psychological, Frailty, Quality of Life
- Keywords
- Art, Museum, Quality of Life, Frailty
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 112 participants (actual)
- Lead sponsor
- Nanyang Technological UniversityUniversity, hospital or other
- Collaborators
- National Gallery Singapore, Singapore, Sheffield Hallam University, Université de Montréal
- Study start
- 2 Mar 2021 (actual)
- Primary completion
- 30 Nov 2021 (actual)
- Study completion
- 31 Dec 2021 (actual)
- First posted
- 14 Jul 2023 (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 goal of the Singapore Art-Health RCT is to examine the effect of a standardized 12-week museum -based participatory art program on health condition, well-being, and quality of life in older community dweller, one that adheres to the Montreal Art-Health framework with culturally specific modifications that are fitting to the local Singaporean context.
Participants will be randomized into an intervention group of a passive control group. Participants in the intervention group will be invited to participate in the 12-week Singapore Art-Health Intervention held at the National Gallery Singapore. All participants will be invited to complete four online psychometric assessments. Participants in the intervention group will be invited to completed an additional post-intervention survey and a feasibility focus group.
Detailed description
Background: Population aging continues to be global health challenge. The prevalence of longstanding age-related conditions such as worsening physical, social, and mental health is expected to increase exponentially with a rapidly ageing population. The practice of participatory art in various settings has been found to be effective in the promotion, prevention and management of health and wellbeing conditions across the life span. However, its effect on health condition among the older population, particularly in the Asian context remains to be investigated. In Montreal, findings from a pilot study provided strong evidence to show that a 12-week, standardized "Art-Health" participatory art program had multidimensional positive effects on the health outcomes of older community dwelling participants including improvements in wellbeing, quality of life, and frail condition.
Current Proposal: The current research will adopt and modify the Montreal Art-Health participatory art framework with local cultural specificity (i.e. The Singapore Art-Health Intervention), and tests its effectiveness in healthy and wellness promotion among a sample of Singaporean older adults via a randomized control trial.
Research Design: The study adopts a participatory action research paradigm and a single-site, open-label Randomized Control Trial (RCT) design to develop and examine the effect of a standardized 12-week museum-based participatory art activity on health condition, wellbeing, and quality of life in older community dwellers.
Sampling and Randomization: Allowing for an attrition rate of 5% at follow-up, a target sample of 110 provides 90% power to detect an effect size of 0.55 (based on the results of the pilot study) between the intervention group and the control group at 5% level of significance (two-tailed test). Participants will be randomized into an intervention group of a passive control group. Participants in the intervention group will be invited to participate in the 12-week Singapore A-Health Intervention held at the National Gallery Singapore.
Intervention Design: The Singapore Art-Health Intervention will span 12 weeks, with each weekly session lasting for two hours. The program is designed to impart basic art appreciation skill (formal analysis in art) and art making techniques to participants through engagement with the collection at the museum.
Outcome measures and Data Analysis: All participants will be invited to complete four online psychometric assessments. Participants in the intervention group will be invited to completed an additional post-intervention survey and a feasibility focus group. For the quantitative data, between and within comparisons of outcomes will be conducted by mixed model analysis of variance (ANOVA), repeated measures ANOVA, and pairwise t-tests with Bonferroni correction. The focus group discussions will be analyzed using thematic analysis with a grounded theory approach to provide insights to the participant's experience and impact of the Singapore Art-Health Intervention.
Importance of Research: The current research will develop and test the effectiveness of a culturally-specific Art-Health participatory art program on health and wellness promotion among a sample of Singaporean older adults. Working collaboratively with the National Gallery Singapore in program development and implementation will serve to ensure program sustainability upon research completion. This collaboration will also foster practice and knowledge transfer to accelerate creative ageing in the local society. Moreover, the findings will contribute to an international RCT for evaluating a standardized participatory art framework to address the impact of population ageing. It will be a potential breakthrough in the development of an efficient art and museum program for older adults locally and internationally.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- Intervention group participants will be invited to engaged in a 12-week participatory art program at the gallery. Participants in the control condition will not offered any art-based activities. All participants were advised not to participate in concurrent health art-based interventions during the research period.
| Arm | Type | Receives |
|---|---|---|
| Singapore A-Health Group | Experimental | Behavioral: Singapore A-Health InterventionA 12-week professionally led participatory art program at the gallery with each week comprising one 2-hour art session, totaling 24 hours of museum tours and participatory art activities. |
| Control Group | No intervention | –No art-based activities offered and advised not to participate in concurrent health and art-based interventions during the 12-week research period. |
Who may qualify
- Ages
- 60 to 99 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- individuals above the age of 60,
- fluent in English
- able to access the internet to complete the online psychometric assessments
Key exclusion criteria (2 listed)
- unable to provide informed consent
- diagnosed with mental health conditions
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 |
|---|---|---|
| Singapore A-Health InterventionThe Singapore A-Health Intervention spanned 12 weeks, with each weekly session lasting for two hours. The program is structured around three thematic domains of the past, present, and future. In each thematic domain consisting of four weeks, participants were tasked with creating an artwork related to the theme and incorporating the learned art techniques. The structure of each thematic domain follows the same structure: the first week involved a 45-minute docent-led gallery tour on three selected pieces of artworks, followed by a 75-minute artist-led brainstorming session where participants were introduced to the techniques and discuss ideas on the artwork to be created. The subsequent three sessions involved further guidance from the artist and a scaffolded delivery of art techniques for participants to incorporate their learning to their artwork. At the end of each domain, there was a showcase where participants present their artwork. | Behavioural | Singapore A-Health Group |
Primary outcome
Quality of Life (EQ5D)
Time frame: Baseline
Quality of life will be assessed by EuroQol-5D (EQ5D) which comprised of two parts: (1) 5-item scale on mobility, self-care, daily activities, pain, and depressive symptoms, (2) a visual analog scale of the participant's perceived health ranging from 0 (worst health) to 100 (best health one can imagine)
Change in Quality of Life (EQ5D)
Time frame: 5-week follow-up
Quality of life will be assessed by EuroQol-5D (EQ5D) which comprised of two parts: (1) 5-item scale on mobility, self-care, daily activities, pain, and depressive symptoms, (2) a visual analog scale of the participant's perceived health ranging from 0 (worst health) to 100 (best health one can imagine)
Change in Quality of Life (EQ5D)
Time frame: 9-week follow-up
Quality of life will be assessed by EuroQol-5D (EQ5D) which comprised of two parts: (1) 5-item scale on mobility, self-care, daily activities, pain, and depressive symptoms, (2) a visual analog scale of the participant's perceived health ranging from 0 (worst health) to 100 (best health one can imagine)
Change in Quality of Life (EQ5D)
Time frame: 12-week follow-up
Quality of life will be assessed by EuroQol-5D (EQ5D) which comprised of two parts: (1) 5-item scale on mobility, self-care, daily activities, pain, and depressive symptoms, (2) a visual analog scale of the participant's perceived health ranging from 0 (worst health) to 100 (best health one can imagine)
Mental Wellbeing (WEMWBS)
Time frame: Baseline
Mental Wellbeing will be assessed by Warwick-Edinburgh Mental Wellbeing Scales (WEMWBS), a 14-item scale assessing various domains of wellbeing.
Change in Mental Wellbeing (WEMWBS)
Time frame: 5-week follow-up
Mental Wellbeing will be assessed by Warwick-Edinburgh Mental Wellbeing Scales (WEMWBS), a 14-item scale assessing various domains of wellbeing.
Change in Mental Wellbeing (WEMWBS)
Time frame: 9-week follow-up
Mental Wellbeing will be assessed by Warwick-Edinburgh Mental Wellbeing Scales (WEMWBS), a 14-item scale assessing various domains of wellbeing.
Change in Mental Wellbeing (WEMWBS)
Time frame: 12-week follow-up
Mental Wellbeing will be assessed by Warwick-Edinburgh Mental Wellbeing Scales (WEMWBS), a 14-item scale assessing various domains of wellbeing.
Frailty (CESAM)
Time frame: Baseline
Frailty will be assessed by the Centre of Excellence on Longevity Self-administered Questionnaire (CESAM). It is a 20-item scale assessing multiple aspects of health such as drug intake, memory complaints, health service utilization, and activities of daily living.
Change in Frailty (CESAM)
Time frame: 5-week follow-up
Frailty will be assessed by the Centre of Excellence on Longevity Self-administered Questionnaire (CESAM). It is a 20-item scale assessing multiple aspects of health such as drug intake, memory complaints, health service utilization, and activities of daily living.
Change in Frailty (CESAM)
Time frame: 9-week follow-up
Frailty will be assessed by the Centre of Excellence on Longevity Self-administered Questionnaire (CESAM). It is a 20-item scale assessing multiple aspects of health such as drug intake, memory complaints, health service utilization, and activities of daily living.
Change in Frailty (CESAM)
Time frame: 12-week follow-up
Frailty will be assessed by the Centre of Excellence on Longevity Self-administered Questionnaire (CESAM). It is a 20-item scale assessing multiple aspects of health such as drug intake, memory complaints, health service utilization, and activities of daily living.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jul 2023.
- Background: PubMed 34654525Beauchet O, Cooper-Brown LA, Hayashi Y, Deveault M, Ho AHY, Launay CP. Health benefits of "Thursdays at the Montreal Museum of Fine Arts": Results of a randomized clinical trial. Maturitas. 2021 Nov;153:26-32. doi: 10.1016/j.maturitas.2021.07.013. Epub 2021 Jul 31.
- Background: PubMed 32143777Beauchet O, Bastien T, Mittelman M, Hayashi Y, Hau Yan Ho A. Participatory art-based activity, community-dwelling older adults and changes in health condition: Results from a pre-post intervention, single-arm, prospective and longitudinal study. Maturitas. 2020 Apr;134:8-14. doi: 10.1016/j.maturitas.2020.01.006. Epub 2020 Jan 13.
- Derived from this study: PubMed 38188333Ho AHY, Ma SHX, Tan MKB, Bajpai R, Goh SSN, Yeo G, Teng A, Yang Y, Galery K, Beauchet O. Effects of participatory 'A'rt-Based Activity On 'Health' of Older Community-Dwellers: results from a randomized control trial of the Singapore A-Health Intervention. Front Med (Lausanne). 2023 Dec 21;10:1238562. doi: 10.3389/fmed.2023.1238562. eCollection 2023.
- Individual participant dataSharing planned: No. There are currently no plans o make individual participant data (IPD) available to other researchers.
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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.
Andy HY Ho, PhD, EdD principal investigator
Nanyang Technological University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Singapore A-Health Intervention in people with Art and Wellness, Psychological, run by Nanyang Technological University 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?
The sponsor lists 3 inclusion and 2 exclusion criteria. 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: finished, as of the sponsor's last update on 14 Jul 2023. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Quality of Life (EQ5D) (time frame: Baseline). The study lists 12 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05945589, which also lists 3 linked publications.
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 14 Jul 2023.