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Prediction of REsponse to Depression Interventions Using Clinical and TD-fNIRS Measurements

NCT06002100 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 540

Last updated 2025-12-12

No results posted yet for this study

Summary

The purpose of the current study is to perform a unified, homogeneous data collection protocol that includes a large cohort of patients undergoing different treatment options for Major Depressive Disorder (MDD) as an avenue for investigating optimal biomarkers for depression treatments on an individual patient level.

Conditions

Interventions

OTHER

fNIRS measurement

Kernel Flow2 measurements.

Sponsors & Collaborators

  • Kernel

    lead INDUSTRY

Principal Investigators

  • Katherine Perdue, PhD · Kernel

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-14
Primary Completion
2026-08-31
Completion
2026-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06002100 on ClinicalTrials.gov