search
Back to results

A Randomized-Controlled Trial to Investigate the Effect of a Novel Music Therapy Application to Reduce Anxiety and Stress

Primary Purpose

Anxiety, Depression, Stress

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
SoundMind App
Spotify Playlist
Sponsored by
SoundMind
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Anxiety

Eligibility Criteria

18 Years - 28 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Male or female Between 18-28 years of age Self-reported concerns around anxiety, stress, or depression Generally healthy - don't live with any uncontrolled chronic disease Must have headphones Exclusion Criteria: Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders Women who are pregnant, breastfeeding or attempting to become pregnant Unwilling to follow the study protocol Testing any other product for any other research studies at the same time History of epilepsy or seizures

Sites / Locations

  • Citruslabs

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

No Intervention

Arm Label

Intervention Group

Spotify Group

Control Group

Arm Description

Participants will listen to the SoundMind app for 20 minutes per day, ideally during a moment of stress.

Participants will listen to a specified Spotify playlist for 20 minutes per day, ideally during a moment of stress.

This group will have no tasks prescribed.

Outcomes

Primary Outcome Measures

Change in scores on the Generalized Anxiety Disorder 7-item scale (GAD-7). [Baseline to Week 6]
The GAD-7 is a self-report questionnaire used to assess the severity of generalized anxiety disorder. It consists of seven questions that ask about the frequency and intensity of common symptoms of anxiety over the past two weeks. Each question is scored on a scale from 0 to 3, with the total scores ranging from 0 to 21. The scoring is typically interpreted as follows: 0-4: Minimal anxiety 5-9: Mild anxiety 10-14: Moderate anxiety 15-21: Severe anxiety
Change in scores on the Patient Health Questionnaire-9 (PHQ-9). [Baseline to Week 6]
The PHQ-9 is a self-report questionnaire used to assess the severity of depression symptoms. Each question is scored on a scale from 0 to 3, with the total scores ranging from 0 to 27. The scoring is typically interpreted as follows: 0-4: Minimal depression 5-9: Mild depression 10-14: Moderate depression 15-19: Moderately severe depression 20-27: Severe depression
Change in scores on the Perceived Stress Scale (PSS). [Baseline to Week 6]
The PSS is a widely used self-report questionnaire designed to measure an individual's perception of stress in their life. Higher scores indicate higher perceived stress.
Change in scores on the World Health Organization Well-Being Index (WHO-5). [Baseline to Week 6]
The WHO-5, or World Health Organization Well-Being Index, is a self-reported questionnaire used to measure psychological well-being and mood. Respondents are asked to rate statements on a scale from 0 to 5, where 0 indicates "at no time" and 5 indicates "all of the time." The scores are summed, resulting in a total score that can range from 0 to 25. A total score of 0-13 suggests poor well-being and a higher risk of depression. A total score of 14-17 indicates moderate well-being. A total score of 18-25 suggests good well-being.

Secondary Outcome Measures

Changes in participant-perceived sleep quality. [Baseline to Week 6]
Survey-based assessment of participants' perception of their sleep quality.

Full Information

First Posted
August 27, 2023
Last Updated
August 27, 2023
Sponsor
SoundMind
Collaborators
Citruslabs
search

1. Study Identification

Unique Protocol Identification Number
NCT06021821
Brief Title
A Randomized-Controlled Trial to Investigate the Effect of a Novel Music Therapy Application to Reduce Anxiety and Stress
Official Title
A Randomized-Controlled Trial to Investigate the Effect of a Novel Music Therapy Application to Reduce Anxiety and Stress
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
May 29, 2023 (Actual)
Primary Completion Date
July 26, 2023 (Actual)
Study Completion Date
July 26, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
SoundMind
Collaborators
Citruslabs

4. Oversight

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

5. Study Description

Brief Summary
This virtual, open-label, three-group, randomized-controlled trial will last six weeks. Participants will be allocated into three groups; the Intervention Group, Spotify Group, and Control Group. All participants will complete a baseline questionnaire before completing their designated regime daily for six weeks. In addition, participants will complete study-specific surveys and validated questionnaires at the end of each week (Week 1, 2, 3, 4, 5 & 6). The study will include 75 [participants in total, 25 per group, who all have self-reported concerns around anxiety, stress, or depression. Questionnaires will be used to monitor sleep, cognitive ability, and changes in symptoms of anxiety, depression, and stress. Both study-specific questionnaires and validated questionnaires will be utilized, including the Generalized Anxiety Disorder Assessment (GAD-7), the 9-question Patient Health Questionnaire (PHQ-9), Perceived Stress Scale (PSS), and The World Health Organisation- Five Well-Being Index (WHO-5). Likert scale responses will be examined from baseline to each check-in. Participant responses on product feedback will be presented as % scores.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Depression, Stress

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Three-group study.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
Participants will listen to the SoundMind app for 20 minutes per day, ideally during a moment of stress.
Arm Title
Spotify Group
Arm Type
Active Comparator
Arm Description
Participants will listen to a specified Spotify playlist for 20 minutes per day, ideally during a moment of stress.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
This group will have no tasks prescribed.
Intervention Type
Other
Intervention Name(s)
SoundMind App
Intervention Description
he SoundMind application uses binaural beats to encourage relaxation, focus, and alertness.
Intervention Type
Other
Intervention Name(s)
Spotify Playlist
Intervention Description
Participants will listen to a "calm vibes" playlist by Spotify.
Primary Outcome Measure Information:
Title
Change in scores on the Generalized Anxiety Disorder 7-item scale (GAD-7). [Baseline to Week 6]
Description
The GAD-7 is a self-report questionnaire used to assess the severity of generalized anxiety disorder. It consists of seven questions that ask about the frequency and intensity of common symptoms of anxiety over the past two weeks. Each question is scored on a scale from 0 to 3, with the total scores ranging from 0 to 21. The scoring is typically interpreted as follows: 0-4: Minimal anxiety 5-9: Mild anxiety 10-14: Moderate anxiety 15-21: Severe anxiety
Time Frame
6 weeks
Title
Change in scores on the Patient Health Questionnaire-9 (PHQ-9). [Baseline to Week 6]
Description
The PHQ-9 is a self-report questionnaire used to assess the severity of depression symptoms. Each question is scored on a scale from 0 to 3, with the total scores ranging from 0 to 27. The scoring is typically interpreted as follows: 0-4: Minimal depression 5-9: Mild depression 10-14: Moderate depression 15-19: Moderately severe depression 20-27: Severe depression
Time Frame
6 weeks
Title
Change in scores on the Perceived Stress Scale (PSS). [Baseline to Week 6]
Description
The PSS is a widely used self-report questionnaire designed to measure an individual's perception of stress in their life. Higher scores indicate higher perceived stress.
Time Frame
6 weeks
Title
Change in scores on the World Health Organization Well-Being Index (WHO-5). [Baseline to Week 6]
Description
The WHO-5, or World Health Organization Well-Being Index, is a self-reported questionnaire used to measure psychological well-being and mood. Respondents are asked to rate statements on a scale from 0 to 5, where 0 indicates "at no time" and 5 indicates "all of the time." The scores are summed, resulting in a total score that can range from 0 to 25. A total score of 0-13 suggests poor well-being and a higher risk of depression. A total score of 14-17 indicates moderate well-being. A total score of 18-25 suggests good well-being.
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Changes in participant-perceived sleep quality. [Baseline to Week 6]
Description
Survey-based assessment of participants' perception of their sleep quality.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
28 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or female Between 18-28 years of age Self-reported concerns around anxiety, stress, or depression Generally healthy - don't live with any uncontrolled chronic disease Must have headphones Exclusion Criteria: Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders Women who are pregnant, breastfeeding or attempting to become pregnant Unwilling to follow the study protocol Testing any other product for any other research studies at the same time History of epilepsy or seizures
Facility Information:
Facility Name
Citruslabs
City
Santa Monica
State/Province
California
ZIP/Postal Code
90404
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

A Randomized-Controlled Trial to Investigate the Effect of a Novel Music Therapy Application to Reduce Anxiety and Stress

We'll reach out to this number within 24 hrs