Quality of LifeNCT06489834
Group Drumming for Improving the Health of Community-Dwelling Elderly
A study testing Group Drumming in people with Quality of Life and Depression, run by KK Women's and Children's Hospital at 1 site in Singapore.
Trial summary
The study seeks to examine the effects that recreational group drumming has on the health of the community- dwelling elderly. It is hypothesized that it has positive and sustainable effects on various health outcome measures. Read more about this study
- Who is it for?
- Ages 60 to 100 yearsHealthy volunteers can take part
- Conditions the study is for
- Quality of Life, Depression, Sleep
- What is being tested?
- Group Drumming
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 300 participants
- Where
- 1 siteSingapore
- Study dates
- 1 Jul 2024to 30 Jun 2026
- 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 60 to 100 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Individuals who are:
- Aged 60 years old and above (by year of age)
- Able to understand English and/or Mandarin, and
- Able to engage in the group drumming activity conducted (e.g. capable of light exercises while seated)
Who cannot join
- Individuals who are:
- On palliative care, and/or
- Bed-bound
- Have severe hearing impairment such that they are unable to engage in group drumming sessions
Trial locations and contacts
1 site in 1 country.
About this study
The study seeks to examine the effects that recreational group drumming has on the health of the community- dwelling elderly. It is hypothesized that it has positive and sustainable effects on various health outcome measures.
Read the detailed description
The study seeks to examine the effects that recreational group drumming has on the health of the community- dwelling elderly. It is hypothesized that it has positive and sustainable effects on various health outcome measures.
One of the primary outcome measure is the quality of life of the participants, which will be measured using the European Quality of Life-5 Dimensions (EQ5D). It is a measure of health status from the EuroQoL. Group primarily designed for self-completion by respondents and is validated locally. The score ranges from 0 (death) to 1 (full health), with 5 dimensions comprising of mobility, self-care, usual activities, pain/discomfort and anxiety/ depression.
The other primary outcome measures include:
- The Geriatric Depression Scale (GDS), which is a tool used for elderly population to evaluate the level of depressive symptoms of an individual over the past week, has been validated locally. It is a self-reported questionnaire consisting of 15 items. Maximum score of 15 and minimum of 0. Score equal or greater than 6 out of 15 is considered to be indicator of depression. ii. The Pittsburgh Sleep Quality Index (PSQI) is a self-reported measure of sleep quality. It is a 19-item scale grouped into 7 equally weighted component scores. The global score ranges from 0 to 21, with poorer sleep quality indicated by a higher global score. iii. (Social Effects) The Lubben Social Network Scale (LSNS) is a self-reported measure designed to gauge social isolation in the elderly. It measures frequency, size and closeness of contacts for the participant's social network by assessing the participant's perceived level of support received from friends and families.
The secondary outcomes are broadly categorized into psychological effects, social effects, and physical effects as listed below:
- Psychological Effects The Mini Mental State Examination (MMSE) is a commonly used screening tool for cognitive impairment worldwide. A score of less than 25 out of maximum of 30 is often suggestive of an underlying cognitive impairment.
- Physical Effects
- Resting blood pressure and heart rate ii. Grip strength - popular indicator of physical functioning iii. Minnesota Manual Dexterity Test
It is hypothesized that recreational group drumming has positive and sustainable effects on various health outcome measures.
The research study will be conducted in two phases. Phase 1 is the randomized controlled study comparing the intervention with independent concurrent controls. Phase 2 will involve providing the intervention to the control subjects from phase 1, where subjects act as their own controls pre to post intervention.
Each drumming session would have 20 participants, excluding two facilitators. This 'Bridging Rhythm with Wellness Programme' will be organised by Lions Befrienders Singapore. These drumming sessions will be held in the Active Ageing Centres (AACs) under Lions Befirenders.
Recruited study participants will be issued Study ID upon enrolment into study. Phase 1 Phase 1 is a randomized controlled trial with a planned ratio of participants of 1:1 in the intervention group (Group A) and control group (Group B). Unlike the pilot study, a crossover will not be conducted in view of (i) difficulties in quantifying a sufficient washout period for such an intervention and (ii) a possible learned effect being carried over.
Participants will be recruited from senior activity centre and randomized into either group within their respective senior activity centre.
All participants in phase 1, be it those randomised into control or intervention group, will be subjected to the following study procedures.
Clinical and patient related outcome data will be collected at the participants' respective senior activity centres at 4 time points:
- At the start of the study
- Midpoint of intervention (Week 4)
- Completion of intervention (Week 8)
- 4 Weeks post-intervention (Week 12) For assessments done at first study timepoint (i.e. start of study assessments), it can be completed 2-3 weeks prior to commencement of each centre's drumming session. This is to allow study team members to have time to complete the required baseline assessments prior to commencement of study intervention.
All study assessments to be completed within study timepoint week with 3 working date window period before and after study timepoint week.
Participants will be asked to complete the following questionnaires and clinical tests:
- European Quality of Life-5 Dimensions (EQ5D)
- Geriatric Depression Scale (GDS)
- Pittsburgh Sleep Quality Index (PSQI)
- Mini Mental State Examination (MMSE)
- Lubben Social Network Scale (LSNS)
- Katz ADL
- Blood Pressure
- Heart Rate
- Grip Strength with Dynamometer
- Minnesota Manual Dexterity Test
- Study Data Collection Form Study participants may be contacted via phone calls to complete required questionnaires. Participants will be provided a research letter if any incidental finding have been found.
Phase 2 In phase 2, subjects in Group B or control group in phase 1, will be offered the opportunity to undergo the intervention at least 4 weeks after the intervention group has concluded Phase 1. Being control subjects in phase 1, these subjects have the baseline values for various measures accurately established prior to intervention. These subjects will act as their own controls, and the effect of the intervention will be assessed by comparing the post treatment values against the baseline measures prior to intervention.
Similar outcome measures will be measured at the time points relative to the baseline measurements, for both phase 1 and phase 2 studies.
Subjects (Group A of phase 1 and subjects of phase 2) will undergo a group drumming course under the Bridging Rhythm with Wellness Programme, comprising of 8 weekly sessions that last for an hour each. Participants cannot be blinded in the study as whoever playing instruments will be aware of the intervention. To protect against contamination, participants of the two groups will be assessed at different times.
In this group drumming course, a variety of percussion instruments will be used inn these sessions, including the conga, cowbell, Djembe, Ashiko, Tan-tans, Dunun, shakers and wood blocks. These instruments will be rotated among the participants from session to session. Participants will be seated comfortably in a circle on chairs within their assigned group, and the percussion instrument will be placed in front of them within reach. Each session will be led by 2 experienced artist-facilitators skilled in leading group drumming courses (1 fixed main facilitator, 1 co-facilitator). The artist-facilitators will be blinded to the participants' backgrounds, psychological and physical health profiles. Artist-facilitators will encourage free play, expression and interaction amongst participants through playing of instruments.
- Conditions
- Quality of Life, Depression, Sleep, Blood Pressure, Grip
- Being tested
- Group Drumming
- Medical subject headings
- Depression
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Group DrummingOther
Weekly group drumming for 8 weeks
| Study group | Role | What they receive |
|---|---|---|
| Drumming Arm | Active comparator | Participants in this arm will undergo weekly group drumming for 8 weeks. Receives: Other: Group Drumming |
| Waitlist Control Arm | No intervention | Participants in this arm will not undergo any intervention while the intervention arm is ongoing and assessed for comparison. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Health related quality of life
European Quality of Life-5 Dimensions (EQ5D) Will be measured. The score ranges from 0 (death) to 1 (full health), with 5 dimensions comprising of mobility, self-care, usual activities, pain/discomfort and anxiety/ depression.
Measured: 12 weeks
Depression
Geriatric Depression Scores will be measured. Scores will range from 0-15. Those will lower scores will have higher risk of depression
Measured: 12 weeks
Sleep Quality
Pittsburg Sleep quality index will be used to measure this outcome
Measured: 12 weeks
Secondary outcomes (3)
Psychological effects
Mini Mental State Examination (MMSE)will be measured. A score of less than 25 out of maximum of 30 is often suggestive of an underlying cognitive impairment.
Measured: 12 weeks
Resting Blood Pressure
Resting Blood pressure will be measured at baseline and at 12 weeks. Both systolic and diastolic pressure would be captured in mmHg
Measured: 12 weeks
Heart Rate
Resting Heart Rate will be measured at baseline and at 12 weeks. This would be in beats/minute
Measured: 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Jul 2024
- Study start1 Jul 2024
- Primary completion30 Sep 2025 (estimated)
- Study completion30 Jun 2026 (estimated)
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 Quality of LifeStudies of the same condition, open and under way.
- More trials run by KK Women's and Children's HospitalThe sponsor's other registered studies.
- 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
- Randomised
- Intervention model
- Sequential
- Model description
- Waitlist control group study with control group undergoing intervention 8 weeks after intervention group has ceased
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 300 participants (estimated)
Sponsor and investigators
- Lead sponsor
- KK Women's and Children's Hospital
- Sponsor type
- Other government
- Collaborators
- Lions Befriender, Toteboard, Institute of Mental Health, Singapore, National University of Singapore
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06489834
- Sponsor's protocol ID
- 2023-2642
- Status last verified
- Aug 2025
- First submitted
- 28 Jun 2024
- Last updated
- 3 Sep 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Yap AF, Kwan YH, Tan CS, Ibrahim S, Ang SB. Rhythm-centred music making in community living elderly: a randomized pilot study. BMC Complement Altern Med. 2017 Jun 14;17(1):311. doi: 10.1186/s12906-017-1825-x.
PubMed 28615007Smith C, Viljoen JT, McGeachie L. African drumming: a holistic approach to reducing stress and improving health? J Cardiovasc Med (Hagerstown). 2014 Jun;15(6):441-6. doi: 10.2459/JCM.0000000000000046.
PubMed 24983262Miyazaki A, Okuyama T, Mori H, Sato K, Ichiki M, Nouchi R. Drum Communication Program Intervention in Older Adults With Cognitive Impairment and Dementia at Nursing Home: Preliminary Evidence From Pilot Randomized Controlled Trial. Front Aging Neurosci. 2020 Jul 2;12:142. doi: 10.3389/fnagi.2020.00142. eCollection 2020.
PubMed 32714176
Study at a glance
From the registry record, last updated by the sponsor on 3 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Group Drumming for Improving the Health of Community-Dwelling Elderly
- ClinicalTrials.gov ID
- NCT06489834
- Acronym / sponsor ID
- 2023-2642
- Conditions
- Quality of Life, Depression, Sleep, Blood Pressure, Grip
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- KK Women's and Children's HospitalOther government
- Collaborators
- Lions Befriender, Toteboard, Institute of Mental Health, Singapore, National University of Singapore
- Study start
- 1 Jul 2024 (actual)
- Primary completion
- 30 Sep 2025 (estimated)
- Study completion
- 30 Jun 2026 (estimated)
- First posted
- 8 Jul 2024 (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 study seeks to examine the effects that recreational group drumming has on the health of the community- dwelling elderly. It is hypothesized that it has positive and sustainable effects on various health outcome measures.
Detailed description
The study seeks to examine the effects that recreational group drumming has on the health of the community- dwelling elderly. It is hypothesized that it has positive and sustainable effects on various health outcome measures.
One of the primary outcome measure is the quality of life of the participants, which will be measured using the European Quality of Life-5 Dimensions (EQ5D). It is a measure of health status from the EuroQoL. Group primarily designed for self-completion by respondents and is validated locally. The score ranges from 0 (death) to 1 (full health), with 5 dimensions comprising of mobility, self-care, usual activities, pain/discomfort and anxiety/ depression.
The other primary outcome measures include:
- The Geriatric Depression Scale (GDS), which is a tool used for elderly population to evaluate the level of depressive symptoms of an individual over the past week, has been validated locally. It is a self-reported questionnaire consisting of 15 items. Maximum score of 15 and minimum of 0. Score equal or greater than 6 out of 15 is considered to be indicator of depression. ii. The Pittsburgh Sleep Quality Index (PSQI) is a self-reported measure of sleep quality. It is a 19-item scale grouped into 7 equally weighted component scores. The global score ranges from 0 to 21, with poorer sleep quality indicated by a higher global score. iii. (Social Effects) The Lubben Social Network Scale (LSNS) is a self-reported measure designed to gauge social isolation in the elderly. It measures frequency, size and closeness of contacts for the participant's social network by assessing the participant's perceived level of support received from friends and families.
The secondary outcomes are broadly categorized into psychological effects, social effects, and physical effects as listed below:
- Psychological Effects The Mini Mental State Examination (MMSE) is a commonly used screening tool for cognitive impairment worldwide. A score of less than 25 out of maximum of 30 is often suggestive of an underlying cognitive impairment.
- Physical Effects
- Resting blood pressure and heart rate ii. Grip strength - popular indicator of physical functioning iii. Minnesota Manual Dexterity Test
It is hypothesized that recreational group drumming has positive and sustainable effects on various health outcome measures.
The research study will be conducted in two phases. Phase 1 is the randomized controlled study comparing the intervention with independent concurrent controls. Phase 2 will involve providing the intervention to the control subjects from phase 1, where subjects act as their own controls pre to post intervention.
Each drumming session would have 20 participants, excluding two facilitators. This 'Bridging Rhythm with Wellness Programme' will be organised by Lions Befrienders Singapore. These drumming sessions will be held in the Active Ageing Centres (AACs) under Lions Befirenders.
Recruited study participants will be issued Study ID upon enrolment into study. Phase 1 Phase 1 is a randomized controlled trial with a planned ratio of participants of 1:1 in the intervention group (Group A) and control group (Group B). Unlike the pilot study, a crossover will not be conducted in view of (i) difficulties in quantifying a sufficient washout period for such an intervention and (ii) a possible learned effect being carried over.
Participants will be recruited from senior activity centre and randomized into either group within their respective senior activity centre.
All participants in phase 1, be it those randomised into control or intervention group, will be subjected to the following study procedures.
Clinical and patient related outcome data will be collected at the participants' respective senior activity centres at 4 time points:
- At the start of the study
- Midpoint of intervention (Week 4)
- Completion of intervention (Week 8)
- 4 Weeks post-intervention (Week 12) For assessments done at first study timepoint (i.e. start of study assessments), it can be completed 2-3 weeks prior to commencement of each centre's drumming session. This is to allow study team members to have time to complete the required baseline assessments prior to commencement of study intervention.
All study assessments to be completed within study timepoint week with 3 working date window period before and after study timepoint week.
Participants will be asked to complete the following questionnaires and clinical tests:
- European Quality of Life-5 Dimensions (EQ5D)
- Geriatric Depression Scale (GDS)
- Pittsburgh Sleep Quality Index (PSQI)
- Mini Mental State Examination (MMSE)
- Lubben Social Network Scale (LSNS)
- Katz ADL
- Blood Pressure
- Heart Rate
- Grip Strength with Dynamometer
- Minnesota Manual Dexterity Test
- Study Data Collection Form Study participants may be contacted via phone calls to complete required questionnaires. Participants will be provided a research letter if any incidental finding have been found.
Phase 2 In phase 2, subjects in Group B or control group in phase 1, will be offered the opportunity to undergo the intervention at least 4 weeks after the intervention group has concluded Phase 1. Being control subjects in phase 1, these subjects have the baseline values for various measures accurately established prior to intervention. These subjects will act as their own controls, and the effect of the intervention will be assessed by comparing the post treatment values against the baseline measures prior to intervention.
Similar outcome measures will be measured at the time points relative to the baseline measurements, for both phase 1 and phase 2 studies.
Subjects (Group A of phase 1 and subjects of phase 2) will undergo a group drumming course under the Bridging Rhythm with Wellness Programme, comprising of 8 weekly sessions that last for an hour each. Participants cannot be blinded in the study as whoever playing instruments will be aware of the intervention. To protect against contamination, participants of the two groups will be assessed at different times.
In this group drumming course, a variety of percussion instruments will be used inn these sessions, including the conga, cowbell, Djembe, Ashiko, Tan-tans, Dunun, shakers and wood blocks. These instruments will be rotated among the participants from session to session. Participants will be seated comfortably in a circle on chairs within their assigned group, and the percussion instrument will be placed in front of them within reach. Each session will be led by 2 experienced artist-facilitators skilled in leading group drumming courses (1 fixed main facilitator, 1 co-facilitator). The artist-facilitators will be blinded to the participants' backgrounds, psychological and physical health profiles. Artist-facilitators will encourage free play, expression and interaction amongst participants through playing of instruments.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- Waitlist control group study with control group undergoing intervention 8 weeks after intervention group has ceased
| Arm | Type | Receives |
|---|---|---|
| Drumming Arm | Active comparator | Other: Group DrummingParticipants in this arm will undergo weekly group drumming for 8 weeks. |
| Waitlist Control Arm | No intervention | –Participants in this arm will not undergo any intervention while the intervention arm is ongoing and assessed for comparison. |
Who may qualify
- Ages
- 60 to 100 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Aged 60 years old and above (by year of age)
- Able to understand English and/or Mandarin, and
- Able to engage in the group drumming activity conducted (e.g. capable of light exercises while seated)
Key exclusion criteria (4 listed)
- On palliative care, and/or
- Bed-bound
- Have severe hearing impairment such that they are unable to engage in group drumming sessions
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 |
|---|---|---|
| Group DrummingWeekly group drumming for 8 weeks | Other | Drumming Arm |
Primary outcome
Health related quality of life
Time frame: 12 weeks
European Quality of Life-5 Dimensions (EQ5D) Will be measured. The score ranges from 0 (death) to 1 (full health), with 5 dimensions comprising of mobility, self-care, usual activities, pain/discomfort and anxiety/ depression.
Depression
Time frame: 12 weeks
Geriatric Depression Scores will be measured. Scores will range from 0-15. Those will lower scores will have higher risk of depression
Sleep Quality
Time frame: 12 weeks
Pittsburg Sleep quality index will be used to measure this outcome
3 secondary outcomes
Psychological effects
Time frame: 12 weeks
Resting Blood Pressure
Time frame: 12 weeks
Heart Rate
Time frame: 12 weeks
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 3 Sep 2025.
- Background: PubMed 28615007Yap AF, Kwan YH, Tan CS, Ibrahim S, Ang SB. Rhythm-centred music making in community living elderly: a randomized pilot study. BMC Complement Altern Med. 2017 Jun 14;17(1):311. doi: 10.1186/s12906-017-1825-x.
- Background: PubMed 24983262Smith C, Viljoen JT, McGeachie L. African drumming: a holistic approach to reducing stress and improving health? J Cardiovasc Med (Hagerstown). 2014 Jun;15(6):441-6. doi: 10.2459/JCM.0000000000000046.
- Background: PubMed 32714176Miyazaki A, Okuyama T, Mori H, Sato K, Ichiki M, Nouchi R. Drum Communication Program Intervention in Older Adults With Cognitive Impairment and Dementia at Nursing Home: Preliminary Evidence From Pilot Randomized Controlled Trial. Front Aging Neurosci. 2020 Jul 2;12:142. doi: 10.3389/fnagi.2020.00142. eCollection 2020.
- Individual participant dataSharing planned: No
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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 Group Drumming in people with Quality of Life and Depression, run by KK Women's and Children's Hospital 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 4 inclusion and 4 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: under way, not looking for participants, as of the sponsor's last update on 3 Sep 2025. 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?
Health related quality of life (time frame: 12 weeks). The study lists 3 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 NCT06489834, 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 3 Sep 2025; AzTrials last refreshed its copy on 7 Nov 2026.