Ignite Creation Date:
2024-05-06 @ 8:25 PM
Last Modification Date:
2024-10-26 @ 3:27 PM
Study NCT ID:
NCT06374056
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-04-19
First Post:
2024-04-09
Brief Title:
Kintsugi Voice Device Pilot Study
Sponsor:
Kintsugi Mindful Wellness Inc
Organization:
Kintsugi Mindful Wellness Inc
Study Overview
Official Title:
Kintsugi Voice Device SCID-5-CT Pilot Study
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
A prospective single arm non-randomized pilot clinical validation study to evaluate the ability of the Kintsugi Voice Device the Device to aid clinical assessment for depression by comparing its output with a diagnosis made by a clinician using the Structured Clinical Interview for DSM-5 SCID-5-CT for up to 500 English speaking adult patients ages 22 and older living in the United States Recruitment will occur for 1 year and participation will be for up to 2 weeks
Detailed Description:
Depression affects approximately 30 of people every year in the United States Detecting mental health conditions early can help patients get the help they need sooner Machine Learning Devices may be one way to help clinicians identify patients with mental health conditions Clinicians may then be able to help patients receive the right level of care earlier Many researchers are working to increase mental health screening Machine Learning can detect subtle patterns like changes in the voice when someone is experiencing mental health conditions Changes in the voice associated with a mental health condition are voice biomarkers
The purpose of this study is to find correlations between voice and how people sound with clinical diagnoses Kintsugi Mindful Wellness Inc has developed a tool the Kintsugi Voice Device that assesses mental health and conditions like depression by studying the voice The studys goal is to test the ability of the Device to identify depressive symptoms
Up to 500 people will take part in this research Subject recruitment is expected to take up to 1 year Completion of the study activities may take about 2 hours but subjects may stay enrolled for up to 2 weeks based on clinician availability for scheduling the Structured Clinical Interview for DSM-5 SCID interview
Study participants will
Answer brief self-reported eligibility confirmation questionnaires These answers help the researchers understand participant health history
Schedule a teleconference with a licensed Clinical Psychologist to evaluate their mental health over Zoom The Clinical Psychologist will guide participants through the Structured Clinical Interview for DSM-5 Clinical Trials Version SCID-5-CT The Clinical Psychologist will be licensed in the participants state of residence This assessment will be video and audio recorded for quality assurance purposes If participants do not agree to being videotaped andor audio recorded they will be unable to join the study The SCID-5-CT assessment is for research purposes only and is not intended for treatment purposes The results of the SCID will not be shared with participants
On the day of the teleconference with a licensed Clinical Psychologist participants will
Complete three brief self-assessment surveys asking about their electronic device mental health and quality of life the Patient Health Questionnaire-9 PHQ- Generalized Anxiety Disorder-7 GAD-7 and the World Health Organization Quality of Life WHOQOL These assessments will take approximately 15 minutes in total
Participants will provide an audio recording in response to 3 prompts of their choosing The audio recording will be inputted to the Kintsugi Voice Device to receive a prediction of current signs of depression The Kintsugi Voice Device Prediction is for research purposes only and will not be shared with participants
Complete the SCID-5-CT while being videotaped and audio recorded with a licensed psychologist or psychiatrist and participant responses will be recorded The SCID will allow the clinician to assess participants current mental status
This study is intended for research purposes and is not intended for treatment andor diagnostic purposes The risks to this study are minimal andor temporary and short lived The study team has implemented procedures to minimize them wherever possible There is always the potential for breach of confidentiality To minimize this risk all entries are encrypted Researchers de-identify personal information using IDs Researchers will store all data in a secure password protected database and Google Cloud Platform bucket Participation may bring up emotional content which could temporarily impact mood To minimize this risk everyone will be emailed a list of mental health resources
There is no cost to subjects for participation There may be no direct benefit from participation Indirect benefits may include reduction in stress learning more about mental health Knowledge gained from the study could potentially benefit patients in the future
Only personal and health information directly related to the research is collected for safety purposes or as required to provide participants with payment including
Name
Age
Address
Phone Number
Email Address
Demographic information eg race gender and ethnicity
English Proficiency
Emergency Contact Information
Audio recording of the SCID-5-CT
Video recording of the SCID-5CT
Audio recordings in response to prompts
Brief Medical History and Medications
Results of the SCID-5-CT
Device Information
PHQ-9 Responses
GAD-7 Responses
Behavioral and Quality of Life Survey Responses
Identifiable data will be kept for 7 years De-identified data will be kept indefinitely
The purpose of this study is to find correlations between voice and how people sound with clinical diagnoses Kintsugi Mindful Wellness Inc has developed a tool the Kintsugi Voice Device that assesses mental health and conditions like depression by studying the voice The studys goal is to test the ability of the Device to identify depressive symptoms
Up to 500 people will take part in this research Subject recruitment is expected to take up to 1 year Completion of the study activities may take about 2 hours but subjects may stay enrolled for up to 2 weeks based on clinician availability for scheduling the Structured Clinical Interview for DSM-5 SCID interview
Study participants will
Answer brief self-reported eligibility confirmation questionnaires These answers help the researchers understand participant health history
Schedule a teleconference with a licensed Clinical Psychologist to evaluate their mental health over Zoom The Clinical Psychologist will guide participants through the Structured Clinical Interview for DSM-5 Clinical Trials Version SCID-5-CT The Clinical Psychologist will be licensed in the participants state of residence This assessment will be video and audio recorded for quality assurance purposes If participants do not agree to being videotaped andor audio recorded they will be unable to join the study The SCID-5-CT assessment is for research purposes only and is not intended for treatment purposes The results of the SCID will not be shared with participants
On the day of the teleconference with a licensed Clinical Psychologist participants will
Complete three brief self-assessment surveys asking about their electronic device mental health and quality of life the Patient Health Questionnaire-9 PHQ- Generalized Anxiety Disorder-7 GAD-7 and the World Health Organization Quality of Life WHOQOL These assessments will take approximately 15 minutes in total
Participants will provide an audio recording in response to 3 prompts of their choosing The audio recording will be inputted to the Kintsugi Voice Device to receive a prediction of current signs of depression The Kintsugi Voice Device Prediction is for research purposes only and will not be shared with participants
Complete the SCID-5-CT while being videotaped and audio recorded with a licensed psychologist or psychiatrist and participant responses will be recorded The SCID will allow the clinician to assess participants current mental status
This study is intended for research purposes and is not intended for treatment andor diagnostic purposes The risks to this study are minimal andor temporary and short lived The study team has implemented procedures to minimize them wherever possible There is always the potential for breach of confidentiality To minimize this risk all entries are encrypted Researchers de-identify personal information using IDs Researchers will store all data in a secure password protected database and Google Cloud Platform bucket Participation may bring up emotional content which could temporarily impact mood To minimize this risk everyone will be emailed a list of mental health resources
There is no cost to subjects for participation There may be no direct benefit from participation Indirect benefits may include reduction in stress learning more about mental health Knowledge gained from the study could potentially benefit patients in the future
Only personal and health information directly related to the research is collected for safety purposes or as required to provide participants with payment including
Name
Age
Address
Phone Number
Email Address
Demographic information eg race gender and ethnicity
English Proficiency
Emergency Contact Information
Audio recording of the SCID-5-CT
Video recording of the SCID-5CT
Audio recordings in response to prompts
Brief Medical History and Medications
Results of the SCID-5-CT
Device Information
PHQ-9 Responses
GAD-7 Responses
Behavioral and Quality of Life Survey Responses
Identifiable data will be kept for 7 years De-identified data will be kept indefinitely
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
True
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None