App boosts therapy for depressed veterans?
NCT ID NCT04002063
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether adding a smartphone app (CBT MobileWork-V) to standard cognitive behavioral therapy helps veterans with depression learn and use therapy skills better. Fifteen OEF/OIF/OND veterans with depression took part. The app was designed to make it easier to practice CBT skills at home.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CBT MobileWork-V smartphone app plus cognitive behavioral therapy
- What this could lead to
- If it works, this could give veterans a convenient tool to practice therapy skills and potentially improve depression recovery.
- What could go wrong
- This was a very small pilot study with only 15 participants, so results may not apply widely. The app is an add-on, not a standalone treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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15 people
The number who actually took part.
- Started
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Oct 2022
- Finished
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Mar 2024
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Veteran of OEF/OIF/OND deployments * Depressive severity of at least 10 on the PHQ-9 at screening (Patient may also have a DSM-5 56 diagnosis of unipolar Major Depression; PTSD; any anxiety disorder; substance/alcohol abuse; or adjustment disorder) * Ability to read at the eighth grade level and to provide informed consent * Patients may be taking antidepressants or antianxiety medications where dose has been stable for at least 4 weeks prior to screening evaluation * Must have an Android smartphone * Must be willing to be audio-taped for fidelity ratings Exclusion Criteria: * Diagnoses of schizophrenia, schizo-affective, bipolar, or other psychotic disorder * Serious suicidal risk (Patient responds positively to PHQ-9 question #9) See B.3.4.1. * Severe PTSD (Score greater than 51 on PTSD Checklist for DSM-5) * Severe substance or alcohol dependence (meets DSM-5 criteria of severe)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Clement J. Zablocki VA Medical Center, Milwaukee, WI
Milwaukee, Wisconsin, 53295-0001, United States
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Coatesville VA Medical Center, Coatesville, PA
Coatesville, Pennsylvania, 19320-2040, United States
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Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
Philadelphia, Pennsylvania, 19104-4551, United States
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Jesse Brown VA Medical Center, Chicago, IL
Chicago, Illinois, 60612, United States
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Minneapolis VA Health Care System, Minneapolis, MN
Minneapolis, Minnesota, 55417-2309, United States
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Rehabilitation R&D Service, Baltimore, MD
Baltimore, Maryland, 21202, United States
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VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX
Dallas, Texas, 75216-7167, United States
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VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
Pittsburgh, Pennsylvania, 15240, United States
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Washington DC VA Medical Center, Washington, DC
Washington D.C., District of Columbia, 20422-0001, United States
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