RECRUITING

A Computerized Depression Intervention in Veterans

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Depressive symptoms are common among Veterans and associated with significant impairment. Timely intervention has the potential to improve mental health outcomes and restore functioning. Interventions delivered through the internet can be completed remotely at any time, and thus minimize burden on Veterans, however the research examining their utility in Veterans is limited. This proposed project will examine Deprexis, a self-guided internet-delivered intervention, which targets depressive symptoms and associated functional impairments. Interviews will be conducted to gain insight into Veterans' perceptions, needs, and preferences vis-a-vis Deprexis, with results informing a randomized controlled trial. Here an 8-week course of Deprexis will be compared to a treatment-as-usual (TAU) control condition to establish if Deprexis is acceptable and effective for Veterans with mild to moderate depressive symptoms. Veterans engaged in Deprexis are hypothesized to show improvements on measures of functioning and decreases in depressive symptoms compared to the TAU control group. The proposed work has great clinical utility, as it could provide a readily accessible, high-quality intervention for the many Veterans suffering from depressive symptoms, with the potential to improve functioning and long-term outcomes.

Official Title

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

Quick Facts

Study Start:2024-05-01
Study Completion:2029-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06217198

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * able to comprehend and sign the informed consent form
  2. * have reliable access to the internet and a computer, tablet and/or smartphone
  3. * exhibit mild or moderate, but not very severe, levels of depression
  4. * stable on psychotropic medications
  1. * endorse any positive symptoms of a psychotic disorder
  2. * screen positive for Bipolar I Disorder
  3. * report current suicidal risk

Contacts and Locations

Study Contact

Rahel R Pearson, PhD
CONTACT
(254) 297-5155
rahel.pearson@va.gov
Joseph F Maher
CONTACT
(254) 743-1478
Joseph.Maher@va.gov

Principal Investigator

Rahel R Pearson, PhD
PRINCIPAL_INVESTIGATOR
Central Texas Veterans Health Care System Waco VA Medical Center, Waco, TX

Study Locations (Sites)

Central Texas Veterans Health Care System Waco VA Medical Center, Waco, TX
Waco, Texas, 76711
United States

Collaborators and Investigators

Sponsor: VA Office of Research and Development

  • Rahel R Pearson, PhD, PRINCIPAL_INVESTIGATOR, Central Texas Veterans Health Care System Waco VA Medical Center, Waco, TX

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-01
Study Completion Date2029-04-30

Study Record Updates

Study Start Date2024-05-01
Study Completion Date2029-04-30

Terms related to this study

Keywords Provided by Researchers

  • Internet-Based Intervention
  • Cognitive-Behavioral Therapy

Additional Relevant MeSH Terms

  • Depression