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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04874077
Other study ID # 2021/03/20
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 21, 2021
Est. completion date September 4, 2021

Study information

Verified date June 2022
Source Kintsugi Mindful Wellness, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Major Depressive Disorder (MDD) is the leading cause of disability worldwide. Depression and anxiety disorders are among the most prevalent of all mental disorders, with an estimated annual prevalence of 9.7% and 18.1% respectively. It has been known for the last 100 years that depression and anxiety both likely affect vocal acoustic properties. In 1921, Emil Kraepelin, characterized depressed patient's voices as having a lower pitch, lower volume, lower rate of speech, more monotony of prosody as well as more hesitations, stuttering, and whispering. Mechanistically, it is possible that the neural circuitry involved in the pathophysiology of mood and anxiety disorders impinge upon the neural circuit involved in speech production, affecting qualities that include rate, prosody, speech latency and other paralinguistic features. Thus, acoustic features of speech may be one of the more readily accessible biomarkers for these conditions. Given this understanding, the investigators sought to develop a passive vocal biomarker instrument for depression and anxiety screening that could markedly expand access as well as standardize the quality of screening in primary care settings.


Recruitment information / eligibility

Status Completed
Enrollment 97
Est. completion date September 4, 2021
Est. primary completion date September 4, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Adult males and or females over the age of 18 at the time of informed consent - Access to a laptop, smartphone or tablet with a functioning microphone - Stated willingness to comply with all study procedures and availability for the duration of the study - Fluency in English - For depressed participant group: Current diagnosis of depression - For non-depressed participant group: No current or prior diagnosis of depression Exclusion Criteria: - Visual impairment that would make it difficult for the participant to follow the instructions - Motor impairment that would make it difficult for the participant to follow the instructions - Any known history of neurodegenerative or Central Nervous System disorders (e.g. MS, Dementia, TBI, Stroke, etc.) - Any known history of major psychiatric disorder other than depression (e.g. Bipolar Disorder, Schizophrenia, etc.) - Any known history of substance abuse

Study Design


Locations

Country Name City State
United States Frontier Psychiatry Billings Montana
United States San Francisco Psychiatrists, Inc. San Francisco California

Sponsors (3)

Lead Sponsor Collaborator
Kintsugi Mindful Wellness, Inc. Frontier Psychiatry, San Francisco Psychiatry Group

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sensitivity and specificity of the Kintsugi's technology's prediction Sensitivity and specificity of the Kintsugi's technology's prediction compared to HAM-D and HAM-A scores. July 30, 2021
Secondary Sensitivity and specificity to depression at the PHQ-9 score of 10 Sensitivity and specificity of the Kintsugi's technology's prediction compared to PHQ-9 scores at a cutoff threshold of 10 July 30, 2021
Secondary Sensitivity and specificity to depression at the GAD-7 score of 10 Sensitivity and specificity of the Kintsugi's technology's prediction compared to GAD-7 scores at a cutoff threshold of 10 July 30, 2021
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