Actively Recruiting
Efficacy of a Novel Web-based Fatigue and Cognitive Assessment Platform in Detecting Fatigue and Depression
Led by Brijesh Patel · Updated on 2026-02-25
100
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
Sponsors
B
Brijesh Patel
Lead Sponsor
S
SmartTec Inc
Collaborating Sponsor
AI-Summary
What this Trial Is About
This observational study evaluates the accuracy of the Okaya AI platform in detecting fatigue and depression among cardiology patients. It compares the platform's assessments to standard screening tools like the PHQ-9 and Fatigue Assessment Scale (FAS). The study aims to address underdiagnosis of these symptoms by using advanced technology to analyze facial and vocal biomarkers during conversations. Participants will complete a single baseline check-in using the Okaya platform, which collects facial expressions, eye contact, speech pitch, volume, and patterns. These features are processed by computer vision and natural language processing to create an AI-based score that reflects fatigue and depression levels. Participants also complete the PHQ-9 and FAS questionnaires for comparison. No treatments or interventions are provided. During the study visit, participants undergo the Okaya assessment and complete the PHQ-9 and FAS questionnaires. Researchers will measure how well the AI-based score correlates with the traditional assessments and evaluate the usability and patient satisfaction with the platform. The study involves a one-time visit and concludes with analysis of baseline data. The total duration of participation is limited to this single assessment.
CONDITIONS
Brief Title
AI Platform for Fatigue and Depression Detection
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age �318 years
- English-speaking
- Able to consent
You will not qualify if you...
- Active substance use
- Nonverbal
- Cognitive disability
- Active suicidal or homicidal ideation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants complete a single baseline check-in using the Okaya platform and standard questionnaires to assess fatigue and depression.
1 visit (in-person or remote)
Trial Site Locations
Total: 2 locations
1
Indiana University
Indianapolis, Indiana, United States, 46074
Not Yet Recruiting
2
Methodist Hospital
Indianapolis, Indiana, United States, 46202
Actively Recruiting
Research Team
B
Brijesh Patel, DO
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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