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Sound Healing for Anxiety: A Randomized Controlled Trial

Primary Purpose

Anxiety, Mental Health Issue, Anxiety Generalized

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Biofield tuning
Sponsored by
Consciousness and Healing Initiative
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Be 18 years or older (≥ 18) Biofield-tuning naive (have never had a session of biofield tuning before) Speak and understand English at a native level Have a score ≥10 on the Generalized Anxiety Disorder 7-item (GAD-7) scale Have regular access to a computer Have experience using a computer Be comfortable using Zoom and completing data collection activities online and over the phone Exclusion Criteria: Suffering from any severe psychological, physical, or cognitive disease or impairment. An active diagnosis or history of suicidality, Post-Traumatic Stress Disorder (PTSD), schizophrenia, or psychotic disorders. This includes history or current suicidality, suicide ideation, and intent to harm self or others. Women who are pregnant or nursing. Having an electronically implanted device, excluding cochlear implants. Currently seeking treatment for an active cancer. Currently has an untreated serious illness (e.g. heart disease, diabetes, etc.).

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Intervention

    Waitlist control

    Arm Description

    Biofield Tuning is a non-invasive, non-medical therapeutic practice in which a resonating tuning fork is used to identify and re-balance off-the-body sites at which perturbations in the tuning fork sound are detected. The description of the intervention has been provided by Biofield Tuning Practitioners and thus describes the practitioner's experience and process while performing the intervention. For this study, the Biofield Tuning practitioner will be using a "hologram" of the participant's body since the intervention will be performed remotely. A "hologram" is when a BT practitioner imagines the body of the participant on the table in front of them. This approach was used successfully for our last feasibility study suggesting an impact of the virtually delivered BT intervention on anxiety.

    The waitlist control group will complete the same weekly self-report questionnaires outlined in the protocol as the intervention group and weekly audio recordings. Following their one-month follow-up questionnaire, those in the waitlist group will be offered a BT session at no cost.

    Outcomes

    Primary Outcome Measures

    Anxiety
    The main objective is to assess whether virtually-delivered biofield tuning can significantly reduce moderate to high levels of generalized anxiety as measured by the State Trait Anxiety Index (STAI).

    Secondary Outcome Measures

    Anxiety 1-month
    We also aim to understand how long BT intervention effects may last with a 1-month follow up as measured by the STAI.
    Positive and Negative Affect
    as measured by the Positive and Negative Affect Scale-Short Form (PANAS)
    Interoceptive awareness
    as measured by the Multidimensional Assessment of Interoceptive Awareness, Version 2 (MAIA-2)
    mental health recovery
    as measured by the Recovery Assessment Scale- Revised (RAS-r). Scores range from 24 to 120. Items are rated from 1 to 5. Higher scores indicate higher levels of recovery.
    stress
    as measured by the Perceived Stress Scale (PSS). Individual scores on the PSS can range from 0 to 40 with higher scores indicating higher perceived stress.
    self compassion
    as measured by the Self-Compassion Scale-Short Form (SCS-SF). The total score is an overall indication of self-compassion, with a higher score indicating more self-compassion.
    perceived social support
    as measured by the Multidimensional Scale of Perceived Social Support (MSPSS)
    relationship with practitioner
    as measured by a Practitioner Relationship questionnaire
    depressive symptoms
    as measured by the PHQ-9

    Full Information

    First Posted
    October 16, 2023
    Last Updated
    October 19, 2023
    Sponsor
    Consciousness and Healing Initiative
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06100406
    Brief Title
    Sound Healing for Anxiety: A Randomized Controlled Trial
    Official Title
    Sound Healing for Anxiety: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 2024 (Anticipated)
    Primary Completion Date
    August 2025 (Anticipated)
    Study Completion Date
    December 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Consciousness and Healing Initiative

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    The goal of this randomized controlled trial is to compare a novel sound healing approach, biofield tuning, to a waitlist control group in a healthy adult population naive to the intervention. The main questions it aims to answer are: Is there a significant reduction in state and trait anxiety as measured by the State-Trait Anxiety Index (STAI) with biofield tuning compared to waitlist control? Are there significant reductions in negative affect, as well as increases in self-compassion, positive affect, and interoceptive awareness in the intervention group? What are the relationships between changes in anxiety symptoms, negative affect words, and microbiome changes in participants who have undergone this biofield intervention? Participants will be: Randomized to intervention/control Recieve 5 sound healing interventions weekly Asked to complete surveys and audio prompts throughout the intervention Asked to provide a microbiome sample pre- and post-intervention
    Detailed Description
    There is an increasing rate of anxiety among the US population, without adequate amounts of resources for treatment. Current pharmacological and psychological treatments for generalized anxiety disorder delivered by doctors, nurses, and clinical psychologists are often expensive and not freely available for many who need effective interventions for anxiety. A novel sound healing approach, Biofield Tuning (BT), has suggested potential benefits to those suffering from generalized anxiety. This intervention, while requiring training and certification, allows for holistic health practitioners to treat anxiety as a complementary mind-body therapy for those seeking relief for anxiety. Intervention. BT is a non-invasive, non-medical therapeutic practice developed by Eileen Day McKusick. BT Practitioners use a tuning fork to identify off-the-body sites at which perturbations in the tuning fork sound are detected. Such sites are described by BT practitioners as storing health-related information within the human biofield. Practitioners describe the process of BT as assessing and clearing perturbations in the human biofield to foster healing. Previous Feasibility Study. Our initial cohort study showed that conducting research for this novel sound healing approach online was feasible and suggested clinical benefits for people struggling with moderate to severe generalized anxiety, as noted in our peer-reviewed scientific publication. This RCT is designed to build upon the previous cohort study by comparing this intervention with a control group to further determine the effectiveness of BT compared to treatment as usual.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Anxiety, Mental Health Issue, Anxiety Generalized, Anxiety State

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Intervention versus waitlist control. The control group will have the option to receive the intervention after the study is completed.
    Masking
    Outcomes Assessor
    Masking Description
    Once randomized, the participants will know they are receiving the intervention. Outcomes assessor will be masked for data analysis.
    Allocation
    Randomized
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention
    Arm Type
    Experimental
    Arm Description
    Biofield Tuning is a non-invasive, non-medical therapeutic practice in which a resonating tuning fork is used to identify and re-balance off-the-body sites at which perturbations in the tuning fork sound are detected. The description of the intervention has been provided by Biofield Tuning Practitioners and thus describes the practitioner's experience and process while performing the intervention. For this study, the Biofield Tuning practitioner will be using a "hologram" of the participant's body since the intervention will be performed remotely. A "hologram" is when a BT practitioner imagines the body of the participant on the table in front of them. This approach was used successfully for our last feasibility study suggesting an impact of the virtually delivered BT intervention on anxiety.
    Arm Title
    Waitlist control
    Arm Type
    No Intervention
    Arm Description
    The waitlist control group will complete the same weekly self-report questionnaires outlined in the protocol as the intervention group and weekly audio recordings. Following their one-month follow-up questionnaire, those in the waitlist group will be offered a BT session at no cost.
    Intervention Type
    Other
    Intervention Name(s)
    Biofield tuning
    Other Intervention Name(s)
    sound healing
    Intervention Description
    Biofield Tuning is a non-invasive, non-medical therapeutic practice in which a resonating tuning fork is used to identify and re-balance off-the-body sites at which perturbations in the tuning fork sound are detected.
    Primary Outcome Measure Information:
    Title
    Anxiety
    Description
    The main objective is to assess whether virtually-delivered biofield tuning can significantly reduce moderate to high levels of generalized anxiety as measured by the State Trait Anxiety Index (STAI).
    Time Frame
    Baseline, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks
    Secondary Outcome Measure Information:
    Title
    Anxiety 1-month
    Description
    We also aim to understand how long BT intervention effects may last with a 1-month follow up as measured by the STAI.
    Time Frame
    1-month post-intervention
    Title
    Positive and Negative Affect
    Description
    as measured by the Positive and Negative Affect Scale-Short Form (PANAS)
    Time Frame
    Baseline, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 1-month post-intervention
    Title
    Interoceptive awareness
    Description
    as measured by the Multidimensional Assessment of Interoceptive Awareness, Version 2 (MAIA-2)
    Time Frame
    Baseline, at 5 weeks
    Title
    mental health recovery
    Description
    as measured by the Recovery Assessment Scale- Revised (RAS-r). Scores range from 24 to 120. Items are rated from 1 to 5. Higher scores indicate higher levels of recovery.
    Time Frame
    Baseline, at 3 weeks, 5 weeks and 1-month post-intervention
    Title
    stress
    Description
    as measured by the Perceived Stress Scale (PSS). Individual scores on the PSS can range from 0 to 40 with higher scores indicating higher perceived stress.
    Time Frame
    Baseline, at 3 weeks, 5 weeks and 1-month post-intervention
    Title
    self compassion
    Description
    as measured by the Self-Compassion Scale-Short Form (SCS-SF). The total score is an overall indication of self-compassion, with a higher score indicating more self-compassion.
    Time Frame
    Baseline, at 3 weeks, 5 weeks and 1-month post-intervention
    Title
    perceived social support
    Description
    as measured by the Multidimensional Scale of Perceived Social Support (MSPSS)
    Time Frame
    Baseline, at 3 weeks, 5 weeks and 1-month post-intervention
    Title
    relationship with practitioner
    Description
    as measured by a Practitioner Relationship questionnaire
    Time Frame
    at 1 week, 3 weeks, and 5 weeks
    Title
    depressive symptoms
    Description
    as measured by the PHQ-9
    Time Frame
    Baseline, at 3 weeks, 5 weeks and 1-month post-intervention
    Other Pre-specified Outcome Measures:
    Title
    Spoken Language
    Description
    As measured by a spoken prompt that will be recorded
    Time Frame
    Baseline, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 1-month post-intervention
    Title
    Microbiome changes
    Description
    as measured by a microbiome sample
    Time Frame
    Baseline and 5 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Be 18 years or older (≥ 18) Biofield-tuning naive (have never had a session of biofield tuning before) Speak and understand English at a native level Have a score ≥10 on the Generalized Anxiety Disorder 7-item (GAD-7) scale Have regular access to a computer Have experience using a computer Be comfortable using Zoom and completing data collection activities online and over the phone Exclusion Criteria: Suffering from any severe psychological, physical, or cognitive disease or impairment. An active diagnosis or history of suicidality, Post-Traumatic Stress Disorder (PTSD), schizophrenia, or psychotic disorders. This includes history or current suicidality, suicide ideation, and intent to harm self or others. Women who are pregnant or nursing. Having an electronically implanted device, excluding cochlear implants. Currently seeking treatment for an active cancer. Currently has an untreated serious illness (e.g. heart disease, diabetes, etc.).
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Lorna C Ciccone, ND
    Phone
    512-284-3655
    Email
    lorna@chi.is
    First Name & Middle Initial & Last Name or Official Title & Degree
    Chloe Tanega
    Email
    chloe@chi.is
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Shamini Jain, PhD
    Organizational Affiliation
    Consciousness and Healing Initiative
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Hemal H Patel, PhD
    Organizational Affiliation
    University of California, San Diego
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Cassandra Vieten, PhD
    Organizational Affiliation
    University of California, San Diego
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    No individual data or identifiers will be shared with other researchers.
    IPD Sharing Time Frame
    2 years
    IPD Sharing Access Criteria
    Subject code blinded. Treatment code blinded and unblinded for analyses.
    Citations:
    PubMed Identifier
    26665043
    Citation
    Jain S, Hammerschlag R, Mills P, Cohen L, Krieger R, Vieten C, Lutgendorf S. Clinical Studies of Biofield Therapies: Summary, Methodological Challenges, and Recommendations. Glob Adv Health Med. 2015 Nov;4(Suppl):58-66. doi: 10.7453/gahmj.2015.034.suppl. Epub 2015 Nov 1.
    Results Reference
    background
    PubMed Identifier
    37023932
    Citation
    Jain S, McKusick E, Ciccone L, Sprengel M, Ritenbaugh C. Sound healing reduces generalized anxiety during the pandemic: A feasibility study. Complement Ther Med. 2023 Jun;74:102947. doi: 10.1016/j.ctim.2023.102947. Epub 2023 Apr 5.
    Results Reference
    result

    Learn more about this trial

    Sound Healing for Anxiety: A Randomized Controlled Trial

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