Acute Effect of Sound Healing on Pain, Fatigue and Mood

March 21, 2023 updated by: Innowage Limited

Acute Effect of Sound Healing on Pain, Fatigue and Mood: A Retrospective Community Based Study

There is evidence that sound healing improves health and well-being. However, sound healing modalities, such as tuning forks, continue to be understudied, especially among people with chronic illnesses. This study examined responses to a single session of sound healing and explored whether responses varied based on analogue pain, fatigue, and mood.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

63

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

People aged between 18-85, having long term illnesses for more than 6-month, completed 30-mins selected sound healing track with tuning forks virtually and shared their impact post session, were evaluated retrospectively.

Description

Inclusion Criteria:

  • People with long term illnesses who attended 'Tuning for Health' virtual session

Exclusion Criteria:

  • Who did not complete 30-mins Sound Healing

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Tuning for Health
Community based group 'Tuning for Health' was set up to provide chronic condition self-management support to people. Trained, experienced therapist-led group used half an hour of sound healing in virtual session.
Over the course of a half-hour virtual session, a specially developed "triple OM track" created by tuning forks was played.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Pain Intensity
Time Frame: From baseline to 30-minutes post intervention
Visual Analogical Scale (VAS) from 0 to 10 scores where 0 describes no pain and 10 worst pain.
From baseline to 30-minutes post intervention
Change in Fatigue
Time Frame: From baseline to 30-minutes post intervention
Visual Analogue Scale for Fatigue (VAS-F) with18 items relating to the subjective experience of fatigue, with each item representing how they currently feel along a visual analogue scale extending between two extremes (e.g., "not at all tired" to "extremely tired").
From baseline to 30-minutes post intervention
Change in Mood
Time Frame: From baseline to 30-minutes post intervention
Visual Analogue Mood Scale using vertical 100 mm lines and schematic faces representing the following mood states: sad, afraid, angry, tired, energetic, happy, and confused.
From baseline to 30-minutes post intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patients Satisfaction
Time Frame: From baseline to 30-minutes post intervention
Patients Satisfaction was measured using 5-Linkert Scale (Very dissatisfied, Somewhat dissatisfied, Neutral, Somewhat satisfied, Very satisfied)
From baseline to 30-minutes post intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Debbi Walker, Suara Sound Academy
  • Principal Investigator: Neha Sharma, PhD, Aarogyam UK CIC

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 24, 2023

Primary Completion (Actual)

March 4, 2023

Study Completion (Actual)

March 5, 2023

Study Registration Dates

First Submitted

March 21, 2023

First Submitted That Met QC Criteria

March 21, 2023

First Posted (Actual)

April 3, 2023

Study Record Updates

Last Update Posted (Actual)

April 3, 2023

Last Update Submitted That Met QC Criteria

March 21, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Inn-AA-SS-002

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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