RecruitingNot ApplicableNCT06923995

Expansion and Evaluation of AI-generated Clinical Assessment (AI-COA®) of Depression and Anxiety Severity

Symptom Evaluation and Quantification for Unified Outcomes and Individualized Assessment


Sponsor

Deliberate Solutions Inc.

Enrollment

120 participants

Start Date

Sep 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The SEQUOIA-1 study evaluates the effectiveness of Artificial Intelligence (AI) in measuring depression and anxiety severity in adults. Investigators from Deliberate Solutions, Inc. and Baylor College of Medicine are conducting this study to determine whether AI can provide reliable clinical assessments of mood and anxiety disorders. In clinical trials for new depression and anxiety treatments, human clinicians typically conduct interviews to evaluate participants' symptoms. These assessments are critical but may vary based on the clinician's experience or interview style, potentially affecting the reliability of research findings. To address this challenge, the study team developed an AI-based Clinical Outcome Assessment tool, called AICOA®, which analyzes video interviews to measure symptoms of depression and anxiety consistently and objectively. AI-COA® has been accepted by the U.S. Food and Drug Administration (FDA) into the Innovative Science and Technology Approaches for New Drugs (ISTAND) pilot program. The primary objectives of the SEQUOIA-1 study are to collect additional data to improve model accuracy and to evaluate model performance across diverse demographic groups. The study also pilots the use of an AI interviewer-an interactive digital agent-to conduct remote assessments. During the study, participants will complete questionnaires about their symptoms and perform brief tasks. Participants will also provide feedback regarding their experience interacting with the AI interviewer. All assessments will be securely video-recorded. Recorded videos will be analyzed by AICOA® to determine depression and anxiety symptom severity. These results will be compared to assessments conducted by human clinicians. The development and validation of reliable, AI-driven assessment tools through this study aim to enhance the accuracy of mental health evaluations, potentially improving the testing and approval processes for new treatments targeting depression and anxiety.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is evaluating whether an AI tool (AI-COA®) can accurately assess how severe someone's depression or anxiety is by analysing their speech and facial expressions during a video call — potentially making it easier to track treatment progress without lengthy in-person appointments. **You may be eligible if...** - You are between 18 and 65 years old - You are fluent in English - You have depression symptoms (HAM-D score above 10) - You have recently started a new treatment for depression or anxiety (within 2–3 weeks) - You have access to a laptop with a working camera and microphone and a stable internet connection - You live in the United States **You may NOT be eligible if...** - You have a cognitive impairment that prevents you from giving consent - You have a visual or hearing impairment that would prevent completing online assessments - You are in a vulnerable population (e.g., incarcerated) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERAI-driven clinical interview

AI-driven clinical interview


Locations(1)

Baylor College of Medicine

Houston, Texas, United States

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NCT06923995


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