- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07267520
The Effects of Quartz Crystal Singing Bowl Music and Guided Relaxation on Mood and Sleep in Rangatahi (Young Adults)
The Effects of Quartz Crystal Singing Bowl Music and Guided Relaxation on Mood and Sleep in Young Adults
The number of people reporting poor mental wellbeing is increasing, with rates exceeding 25% of the population. Rates of psychological distress in young people (aged 15-24 years) are rapidly increasing but many cannot access professional help. Self-help options such as meditation and mindfulness are effective in decreasing stress and enhancing mood, but time, practice, self-motivation and patience are required to fully realise the benefits. Thus, there is a need to explore alternate treatment options.
This study seeks to determine if the effects of listening to quartz crystal singing bowl music (CSBs) are equivalent to that of progressive guided muscle relaxation on self-report measures of mood, stress and sleep in young adults at 4- and 8- weeks post intervention. The intervention will be delivered online.
The main question it aims to answer is:
Are the effects of listening to singing bowl music equivalent to that of progressive guided muscle relaxation (PMR) on self-report measures of mood in young adults (Total Mood Disturbance of the POMS) at 4- and 8- weeks post intervention.
Does listening to singing bowls result in improved sleep and stress, similar to the effects of PMR.
Participants will be allocated to either the singing bowls or progressive muscle relaxation group. They will be sent a link to listen to the intervention 3 times a week for the first 4 weeks, and then weekly for the next 4 weeks. They will be asked to compete an online questionnaire at baseline, 4 weeks and 8 weeks.
At the end of the trial (8 weeks), participants will be given access to both singing bowls and progressive muscle relaxation interventions to use as often as they like.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Waikato Region
-
Hamilton, Waikato Region, New Zealand, 3204
- School of Psychological and Social Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- age 16-25 years
Exclusion Criteria:
- undergoing psychiatric/psychological treatment
- participation in guided relaxation more than once a month
- listened to singing bowls more than once a month
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Progressive Muscle Relaxation
|
A guided progressive muscle relaxation audio (recorded by the NZ Cancer Society https://www.youtube.com/watch?v=Zydrp3rfJdY) and similar to the PMR script from the Anxiety and Phobia Workbook by Edmund Bourne was used.
The session took approximately 12 minutes.
Participants were instructed to start by sitting or lying comfortably, taking some deep breaths and then tense and relax muscles in a sequential manner from the head to the feet.
The audio was presented online via Qualtrics software
|
|
Experimental: Quartz Crystal Singing Bowls music
|
The quartz crystal singing bowls audio track used in the current study was "Tranquility" by Annie Jameson.
The audio track was 570 seconds (9.5 minutes) for all sessions.
Annie Jameson composed the track herself and gave permission for its use.
The full Tranquility track can be found on YouTube (https://www.youtube.com/watch?v=0mX3Vqvo5k4) or Spotify.
The audio was accessed online via the Qualtrics platform
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in total mood disturbance (TMD) score between baseline, 4 weeks and 8 weeks
Time Frame: Baseline, 4 weeks and 8 weeks
|
The TMD is derived from the profile of mood states questionnaire (abbreviated version).
Participants are presented with a list of 40 words that describe feelings people have.
They are asked to circle the number that best describes how they feel right now from 0 (not at all), 1 (a little), 2 (moderately), 3 (quite a lot) to 4 (extremely).
Seven subscales are calculated by summing the relevant items (Tension, Anger, Fatigue, Depression, Esteem related affect, Vigour and Confusion).
A Total Mood Disturbance score (TMD) is also calculated by summing the totals for the negative subscales (Tension, Depression, Anger, Fatigue, Confusion), and subtracting the totals for the positive scales (Vigour, Esteem-related Affect [Note that 2 items are reverse scored for the ERA subscale].
A higher score reflects a more negative mood state
|
Baseline, 4 weeks and 8 weeks
|
|
Change in total mood disturbance (TMD) score between baseline, 4 weeks and 8 weeks
Time Frame: Baseline, 4 weeks and 8 weeks
|
The TMD is derived from the profile of mood states questionnaire (abbreviated version).
Participants are presented with a list of 40 words that describe feelings people have.
They are asked to circle the number that best describes how they feel right now from 0 (not at all), 1 (a little), 2 (moderately), 3 (quite a lot) to 4 (extremely).
Seven subscales are calculated by summing the relevant items (Tension, Anger, ERA-score range 0-24; Fatigue, Vigour, Confusion- score range 0-20; Depression - score range 0-28 ).
A Total Mood Disturbance score (TMD) is also calculated by summing the totals for the negative subscales (Tension, Depression, Anger, Fatigue, Confusion), and subtracting the totals for the positive scales (Vigour, Esteem-related Affect).
A constant (100) can be added to eliminate negative values.
Scores (including the constant) range from 52-216.
A higher score reflects a more negative mood state
|
Baseline, 4 weeks and 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in POMS subscale scores at 4 and 8 weeks
Time Frame: Baseline, 4 weeks and 8 weeks
|
The POMS has seven subscales: Tension, Anger, Fatigue, Depression, Esteem related affect, Vigour and Confusion.
For the negative subscales (Tension, fatigue, confusion, depression and anger), a higher score indicates poorer mood.
For the positive subscales (vigour and esteem related affect), a high score indicates a more positive mood.
|
Baseline, 4 weeks and 8 weeks
|
|
Overall sleep quality
Time Frame: Baseline, 4 weeks, 8 weeks
|
Rating of overall sleep quality from the Auckland Sleep questionnaire.
Higher ratings (on a 1-4 scale) indicate poorer sleep quality
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Baseline, 4 weeks, 8 weeks
|
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Visual analogues scales - immediately before and after a session
Time Frame: Once a week for 8 weeks
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To assess the acute effects of the intervention, participants will be asked to complete ratings of overall mood, relaxation, and stress before and after one session one session each week.
Participants are asked to rate how they are feeling right now using a visual analogue scale (VAS) from 0 (worst I've ever felt not relaxed, not stressed,) to 100 (very stressed, very relaxed, best I've ever felt)
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Once a week for 8 weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Nicola J Starkey, Starkey, University of Waikato
- Principal Investigator: Michael Jameson, University of Auckland, New Zealand
Publications and helpful links
General Publications
- Goldsby TL, Goldsby ME, McWalters M, Mills PJ. Effects of Singing Bowl Sound Meditation on Mood, Tension, and Well-being: An Observational Study. J Evid Based Complementary Altern Med. 2017 Jul;22(3):401-406. doi: 10.1177/2156587216668109. Epub 2016 Sep 30.
- Matthews A, Phillips MC, Matthews LR, Kumar S, Pillai A, Jameson MB. A Pilot Study Evaluating the Effects of Relaxation Music Played on Quartz Crystal Singing Bowls on Mood in Teenage Males. J Psychiatry Behav Sci. 2023;6(2):1085
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 (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HREC(Health)2024#3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
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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