Multi-Omic, Clinomic and Digitomic Attributes of Major Depression for Integrative Analytics
Part of paid clinical trials in Jacksonville, Florida.
- Sponsor
- Mayo Clinic
- Study ID
- NCT05910957
- Status
- Enrolling By Invitation
Conditions
- Major Depressive Disorder
- Unipolar, Non-psychotic Major Depressive Disorder
Eligibility Criteria
- Sex
- ALL
- Age
- 20 Years - 62 Years
- Healthy Volunteers
- Not accepted
Study Details
The purpose of this research is to see if information from blood and data from smartwatches can be combined to help diagnose depression and determine if transitions between active depression and treated depression can be predicted.
Key Dates
- Start date
- Aug 2, 2023
- Status verified
- Jul 2025
- Primary completion
- Jun 6, 2026
- Completion
- Dec 6, 2026
Study Design
- Enrollment
- 40 participants (estimated)
Arms
- Arm: Non-depressed controlsSubjects without depression will fill out questionnaires about their general health and wellbeing, quality of life, mental health, emotional health, suicide risk, support system, and childhood experiences. Smartwatch data will also be collected to monitor step count, sleep quality, heart rate (resting and active), and activity rates.
- Arm: Antidepressant-treated adultsSubjects diagnosed with depression will fill out questionnaires about their general health and wellbeing, quality of life, mental health, emotional health, suicide risk, support system, and childhood experiences. Smartwatch data will also be collected to monitor step count, sleep quality, heart rate (resting and active), and activity rates.
Primary Outcome Measure
Change in Quick Inventory of Depressive Symptoms-Clinician Rated (QIDS-CR) scale [ Time Frame: Baseline, 4 weeks, and 8 weeks ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Mayo Clinic Florida | Jacksonville | Florida | 32224 | - |
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