Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06217198

A Randomized Controlled Trial of Deprexis Evaluating a Computerized Intervention to Decrease Depression and Restore Functioning in Veterans

Led by VA Office of Research and Development · Updated on 2025-07-14

152

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Depression is a common issue among Veterans and can lead to serious difficulties in daily functioning and quality of life. This research aims to evaluate Deprexis, a self-guided internet program designed to reduce depressive symptoms and improve functioning in Veterans with mild to moderate depression. The study seeks to understand Veterans' views on Deprexis and test its effectiveness compared to usual care in a controlled trial setting. Participants will be randomly assigned to either an 8-week course of Deprexis, which includes interactive modules to help manage depression, or continue with their usual treatment. The study will first gather feedback from a smaller group of Veterans to improve the program and then conduct a larger trial to compare outcomes between those using Deprexis and those receiving standard care. Throughout the study, Veterans will complete assessments measuring depression symptoms and functional ability at the start, after 8 weeks, and again 8 weeks later. Researchers will analyze these results to see if Deprexis helps reduce symptoms and improve daily functioning. The study aims to provide accessible, low-cost support for Veterans experiencing depression, potentially helping to reduce long-term disability and suicide risk.

CONDITIONS

Brief Title

A Computerized Depression Intervention in Veterans

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female Veterans of any race or ethnicity
  • Able to understand and sign the informed consent form
  • Have reliable access to the internet and a device such as a computer, tablet, or smartphone
  • Exhibit mild to moderate depression levels
  • Stable on psychotropic medications if applicable
Not Eligible

You will not qualify if you...

  • Presence of any positive symptoms of a psychotic disorder
  • Screening positive for Bipolar I Disorder
  • Current suicidal risk reported

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) to assess eligibility

Outpatient Treatment

Duration - 8 weeks

Participants engage in an 8-week course of Deprexis, a self-guided internet-delivered behavioral intervention for depressive symptoms and related functional impairment.

Participants use the online program independently; assessments occur at baseline and post-treatment

Follow-up

Duration - 8 weeks

Participants complete follow-up assessments 8 weeks after treatment to evaluate lasting effects on depressive symptoms and functioning.

1 follow-up assessment visit (remote or in-person)

Trial Site Locations

Total: 1 location

1

Central Texas Veterans Health Care System Waco VA Medical Center, Waco, TX

Waco, Texas, United States, 76711

Actively Recruiting

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Research Team

R

Rahel R Pearson, PhD

J

Joseph F Maher

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

The Evaluation of a Web-Based Intervention (Deprexis) to Decrease Depression and Restore Functioning in Veterans: Protocol for a Randomized Controlled Trial.

Rahel Pearson, Christopher G Beevers, Joseph Mignogna...

https://pubmed.ncbi.nlm.nih.gov/39446432