- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06513858
Evaluating the Community Drum Circle
Evaluating the Impact of Community-Based Mindfulness and Musical Programs on Psychiatric Measures, Drum Circle Study 2c.
Mental health vulnerability due to stress is increased America due to disproportionate effects of social factors such as racism, poverty, education, and criminal justice sentencing. Various meditation and mindfulness approaches have provided evidence of measured reductions in multiple negative dimensions of stress. However, the majority of these studies do not have an adequate representation of Persons of African Descent(PAD) or other marginalized groups and are not designed to be culturally relevant or community based. Music has been shown to alleviate multiple symptoms of stress and has been shown to be a preferred and effective support for meditation and mindfulness. However, its role in stress management in PADs engaged in meditation or mindfulness is seldom studied. This study aims to evaluate the effects of a community-based music mindfulness program on stress management in PAD community members with anxiety and depression during COVID19.
Component 2c. Drum Circle Study: Investigators will study the impact of participation in drum circles on anxiety and feelings of connectedness.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The investigators also propose a study to investigate the effects of communal drumming in reducing anxiety and increasing connectedness within drum circle community. Investigators hypothesize that these intervention will lead to reductions in scores on stress scales and will provide preliminary data for studies evaluating these types of community programs as an adjunct to the standard of care.
Individuals who attend periodic (i.e. weekly) drum circles will be recruited to join an 8-week paradigm. Drum circle sessions may audio recorded and participants will be informed of this during the consent process. Participants may be asked to undergo Electroencepholography, functional Near Infrared Spectroscopy, and/or other physiological measures before, during, and after the circles. Upon completion of the experiments, participants will be asked to take part in a focus group that will provide valuable feedback on their experience with the mindfulness intervention. Focus groups will last 30-minutes to 1 hour and will occur in-person.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Connecticut
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New Haven, Connecticut, United States, 06515
- BLOOM
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New Haven, Connecticut, United States, 06520
- Musical Intervention Studios
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- ages 16 and older
Exclusion Criteria:
- ages 15 and younger
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: Drum Circle- Cohort 1
Cohort 1 will listen together to recordings of drumming and be allowed to drum along while listening. The facilitator will lead participants in procedures such as checking in (e.g. "How are you doing today?" before and after the circle) and breathing exercise. |
Communal drumming
Recordings of drumming taken from the music made during a previous component of the study
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Active Comparator: Drum Circle Control Group- Cohort 2
Control investigations will also be conducted to better understand the contribution communal drumming has on effects of anxiety and connectedness.
All control investigations will take place in the same space and at the same frequency as the associated experimental arm but with no drumming.
All participants will be asked to complete the same surveys and at the same frequency to those completed in the experimental arm.
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Recordings of drumming taken from the music made during a previous component of the study
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rating of Absorption in music pre vs post sessions
Time Frame: Baseline on day of study visit before drum circle, during drum circle (45min), 30 min after music listening
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These ratings are classified on a scale from 0 to 1, with 0 indicating no absorption and 1 indicating complete absorption.
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Baseline on day of study visit before drum circle, during drum circle (45min), 30 min after music listening
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Altered States of Consciousness Rating Scale
Time Frame: Baseline on day of study visit before drum circle, during drum circle (45min), 30 min after music listening
|
This scale has 94 statements and below each statement is a line with the endpoints "No, not more than usually" and "Yes, much more than usually."
Each participant will rate to what extent the statements apply to their particular experience, compared to normal waking consciousness, by making a vertical mark on the line below the statements.
Normal waking consciousness corresponds to a mark at the very left end of the scale, i.e.: "No, not more than usually."
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Baseline on day of study visit before drum circle, during drum circle (45min), 30 min after music listening
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: AZA Allsop, MD, PhD, Yale University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2000028866_c
- 2R25MH071584-11 (U.S. NIH Grant/Contract)
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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