- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05795322
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
Intervention / Treatment
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
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Leicester, United Kingdom
- Aarogyam UK CIC
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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 |
|---|---|
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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.
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Over the course of a half-hour virtual session, a specially developed "triple OM track" created by tuning forks was played.
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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
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Visual Analogical Scale (VAS) from 0 to 10 scores where 0 describes no pain and 10 worst pain.
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From baseline to 30-minutes post intervention
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Change in Fatigue
Time Frame: From baseline to 30-minutes post intervention
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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").
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From baseline to 30-minutes post intervention
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Change in Mood
Time Frame: From baseline to 30-minutes post intervention
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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.
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From baseline to 30-minutes post intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patients Satisfaction
Time Frame: From baseline to 30-minutes post intervention
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Patients Satisfaction was measured using 5-Linkert Scale (Very dissatisfied, Somewhat dissatisfied, Neutral, Somewhat satisfied, Very satisfied)
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From baseline to 30-minutes post intervention
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
Keywords
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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