Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed No phase listed Observational

Study to Evaluate Potential Predictors of Relapse in Participants With Major Depressive Disorder (MDD)

ClinicalTrials.gov ID: NCT02489305

Public ClinicalTrials.gov record NCT02489305. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 1, 2026, 7:05 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Longitudinal, Observational Study to Evaluate Potential Predictors of Relapse in Subjects With Major Depressive Disorder Who Have Responded to Antidepressant Treatment

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to identify if there are self-reported or objective measures related to mood parameters that can predict near-term relapse (within 1 month or at another identified time point before meeting the criteria for relapse) or early symptomatic changes indicative of relapse prodrome in major depressive disorder (MDD).

Study identification

NCT ID
NCT02489305
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
330 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years to 64 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 15, 2014 (Actual)
Primary completion
May 1, 2018 (Actual)
Completion
May 1, 2018 (Actual)
Last update posted
Feb 3, 2025

2014 – 2018

United States locations

U.S. sites
25
U.S. states
16
U.S. cities
25
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Glendale California — —
Not listed Oceanside California — —
Not listed San Diego California — —
Not listed Sherman Oaks California — —
Not listed Stanford California — —
Not listed Hartford Connecticut — —
Not listed Jacksonville Florida — —
Not listed Orlando Florida — —
Not listed Tampa Florida — —
Not listed Augusta Georgia — —
Not listed Chicago Illinois — —
Not listed Skokie Illinois — —
Not listed Springfield Illinois — —
Not listed Iowa City Iowa — —
Not listed Wichita Kansas — —
Not listed Worcester Massachusetts — —
Not listed Ann Arbor Michigan — —
Not listed Durham North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Philadelphia Pennsylvania — —
Not listed Charleston South Carolina — —
Not listed Dallas Texas — —
Not listed Houston Texas — —
Not listed Salt Lake City Utah — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02489305, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 3, 2025 · Synced Oct 1, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02489305 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →