- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06542003
The Impact of Performing Arts on Mental Health, Social Connection, and Creativity in University Students
Movin' & Groovin' for Wellness: A Drumming and Dancing Program to Support Well-being in NUS Students
The goal of this clinical trial is to investigate whether the "Movin' & Groovin' for Wellness" (MGW) performing arts program is able to support mental, social, and emotional health in NUS students. It will also assess the program's impact on students' well-being. The main questions it aims to answer are:
- Does participation in the program decrease depressive symptoms, stress levels and anxiety?
- Does the program foster creative expression among participants?
- Does the program foster social connections among participants?
Researchers compare the effects of the facilitated music and dance sessions (MGW program) to a Control group that does not participate in these activities. Participants are randomly assigned into either the Experimental (MGW) group or Control group.
Those in the Experimental group are randomly allocated to one of two subgroups, where participants either experience drumming or dancing sessions first (for 5 weeks), followed by the other activity (e.g., the only difference between subgroups is the order in which they experience the facilitated sessions). Both the drumming and dancing sessions are led by trained professionals. The sessions are held weekly for 10 weeks in dedicated performance rooms. Participants also complete questionnaires, and have the opportunity to participate in a focus group discussion to provide feedback about the program.
Control group participants complete the same questionnaires at the same time points without participating in the activities. The program aims to evaluate the effectiveness of music and dance in promoting mental health, social well-being, and creativity among university students.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Singapore, Singapore, 117376
- YST Conservatory, 3 Conservatory Drive
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Be currently enrolled in NUS
- Be between the ages of 18-40 years old
- Be fluent (speak and write) in English
- Able to commit to attending the live sessions for the entire 10-week period
- Have normal or corrected-to-normal hearing and vision
Exclusion Criteria:
- Have been diagnosed with a neurological or hearing impairment, or a physical impairment that would prevent moving/dancing
- Are taking medicine to treat their mental health (as this would be a confound in the study)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MGW Drum and Dance Group
Participants in the intervention group engage in a 10-week program that includes both drumming and dancing sessions.
The group is further divided into two subgroups due to logistical reasons, with one subgroup attending five weeks of drumming sessions followed by five weeks of dancing sessions, and the other subgroup attending sessions in the opposite order.
All participants in this arm participate in both drumming and dancing sessions.
|
Movin' and Groovin' for Wellness (MGW) is a 10-week program consisting of facilitated drumming and dancing sessions.
The sessions include guided activities involving drumming, dancing, and group improvisation.
Each session lasts approximately 1.5 hours, with activities designed to improve mental well-being, enhance social connections, and foster creative expression.
The sessions are guided by professional facilitators.
|
|
No Intervention: No-treatment Control Group
Participants in the control group do not participate in the drumming and dancing sessions.
They represent "normal student life".
They only complete the same questionnaires at the same time points as the intervention group to serve as a baseline comparison for evaluating the impact of the interventions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in depressive symptoms, stress levels and anxiety levels
Time Frame: Baseline, Week 5, Week 10
|
Measurement of participants' depressive symptoms, stress levels and anxiety levels using the Depression, Anxiety, and Stress Scale (DASS-21).
The scores from the DASS-21 questionnaire are used to assess these changes.
Depression/Anxiety/Stress sub-scales' scores can range from 0-21 with higher scores indicating worse symptoms.
|
Baseline, Week 5, Week 10
|
|
Changes in quality of life
Time Frame: Baseline, Week 5, Week 10
|
Measurement of participants' quality of life using the WHO Quality of Life-BREF (WHOQOL-BREF).
This measure captures physical health, psychological health, social relationships, and environmental domains.
The physical, psychological, social, and environmental domain scores each range from 4-20 with higher scores indicating a higher quality of life.
|
Baseline, Week 5, Week 10
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Participant experience
Time Frame: Week 5, Week 10
|
Collection of participants' experience in the program.
The bespoken survey asks about students' experiences in the program, spanning artistic engagement, creative expression, comfort, mood, sense of well-being, and social aspects of the program.
|
Week 5, Week 10
|
|
Qualitative feedback from focus group discussion
Time Frame: Within two weeks post-program completion
|
Collection of lived experience from focus group discussion (FGD) about the program's impact on mental health, social connection, and creativity, as well as general feedback about the MGW program.
|
Within two weeks post-program completion
|
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Changes in social connection
Time Frame: Baseline, Week 5, Week 10
|
Measurement of participants' social networks using the Short Form Lubben Social Network Scale.
This scale evaluates the frequency and quality of participants' social interactions.
The Friend sub-scale scores range from 0-15 with higher scores indicating more social connection with friends.
The Family sub-scale scores range from 0-15 with higher scores indicating greater social connection with family.
|
Baseline, Week 5, Week 10
|
|
Changes in creativity
Time Frame: Baseline, Week 5, Week 10
|
Measurement of participants' creative experiences using the Experience of Creation Scale.
This scale assesses the impact of creative activities on participants' feelings of empowerment, freedom to decide, impact, and creativity.
The scores range from 4-20 with higher scores indicating better experience of creation.
|
Baseline, Week 5, Week 10
|
|
Changes in resilience
Time Frame: Baseline, Week 5, Week 10
|
Measurement of emotional resilience using the Brief Resilient Coping Scale.
This scale measures participants' ability to cope with stress and adapt to changes, with higher scores indicating better resilience.
The scores range from 4-20 with higher scores indicating high resilient copers.
|
Baseline, Week 5, Week 10
|
|
Changes in mood regulation through music
Time Frame: Baseline, Week 5, Week 10
|
Measurement of participants' use of music for mood regulation using the Brief Music in Mood Regulation Scale (B-MMR).
This scale evaluates various strategies of music listening that individuals use to manage their mood and emotions.
For each sub-scale, the scores range from 3-15 with higher scores indicating greater use of that listening strategy for mood regulation.
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Baseline, Week 5, Week 10
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Kathleen R Agres, PhD, National University of Singapore
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- NUS-IRB-2023-3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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