Actively Recruiting

Age: 18Years - 99Years
All Genders
ID07218263

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

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age �318 years
  • English-speaking
  • Able to consent
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

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

Loading map...

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

Similar Trials

"Breathlessness Diagnostics in a Box" (BiaB) for Primary Car...

Breathlessness

Actively Recruiting

3 locations

A Preventive, Multidisciplinary Primary Care Intervention Or...

Vascular Disease

Actively Recruiting

1 location

A Phase 1 Open-label, Multicenter Trial Evaluating Safety an...

Cardiovascular

Actively Recruiting

18 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here