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Healthy Young AdultsNCT07267520

The Effects of Quartz Crystal Singing Bowl Music and Guided Relaxation on Mood and Sleep in Rangatahi (Young Adults)

A study testing Quartz Crystal Singing Bowl music and Progressive Muscle Relaxation in people with Healthy Young Adults, run by The University of Waikato at 1 site in New Zealand.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 16 to 25 yearsHealthy volunteers can take part
Conditions the study is for
Healthy Young Adults
What is being tested?
Quartz Crystal Singing Bowl music and Progressive Muscle Relaxation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
108 participants
Where
1 siteNew Zealand
Study dates
22 Mar 2024to 31 Dec 2024
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 16 to 25 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • age 16-25 years

Who cannot join

  • undergoing psychiatric/psychological treatment
  • participation in guided relaxation more than once a month
  • listened to singing bowls more than once a month

Trial locations and contacts

1 site in 1 country.

New Zealand1 site
  • School of Psychological and Social Sciences

    Hamilton, Waikato Region, 3204

Other trials in New Zealand

About this study

Official title: 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.

Read more

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.

Being tested
Quartz Crystal Singing Bowl music, Progressive Muscle Relaxation
Keywords
Mood, Crystal singing bowls, Progressive muscle relaxation, online intervention

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Quartz Crystal Singing Bowl musicBehavioural

    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

  • Progressive Muscle RelaxationBehavioural

    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

Study groups in NCT07267520
Study groupRoleWhat they receive
Quartz Crystal Singing Bowls musicExperimentalNot described
Receives: Behavioral: Quartz Crystal Singing Bowl music
Progressive Muscle RelaxationActive comparatorNot described
Receives: Behavioral: Progressive Muscle Relaxation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in total mood disturbance (TMD) score between 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

    Measured: Baseline, 4 weeks and 8 weeks

  2. Change in total mood disturbance (TMD) score between 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

    Measured: Baseline, 4 weeks and 8 weeks

Secondary outcomes (3)
  1. Change in POMS subscale scores at 4 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.

    Measured: Baseline, 4 weeks and 8 weeks

  2. Overall sleep quality

    Rating of overall sleep quality from the Auckland Sleep questionnaire. Higher ratings (on a 1-4 scale) indicate poorer sleep quality

    Measured: Baseline, 4 weeks, 8 weeks

  3. Visual analogues scales - immediately before and after a session

    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)

    Measured: Once a week for 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Dec 2025
  2. Study start22 Mar 2024
  3. Primary completion11 Oct 2024
  4. Study completion31 Dec 2024

Resources

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
108 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07267520
Sponsor's protocol ID
HREC(Health)2024#3
Status last verified
Dec 2025
First submitted
24 Nov 2025
Last updated
15 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: All data are available from the PI upon reasonable request

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.

    PubMed 27694559
  • 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

Questions about this trial

What is this clinical trial studying?

A study testing Quartz Crystal Singing Bowl music and Progressive Muscle Relaxation in people with Healthy Young Adults, run by The University of Waikato at 1 site in New Zealand.

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 1 inclusion and 3 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 15 Dec 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 New Zealand. 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?

Change in total mood disturbance (TMD) score between baseline, 4 weeks and 8 weeks (time frame: Baseline, 4 weeks and 8 weeks). The study lists 2 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 NCT07267520, which also lists 2 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 15 Dec 2025.

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