Augmented Depression Therapy (ADepT) Case Series
Part of paid clinical trials in Columbus, Ohio.
- Sponsor
- Ohio State University
- Study ID
- NCT07733310
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Depression / Major Depressive Disorder
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Augmented Depression Therapy (ADepT) — BEHAVIORALADepT is a solution-focused behavioral health intervention that blends techniques from cognitive, behavioral, and acceptance-based treatments to help patients manage symptoms of depression and increase wellbeing. It consists of 15 acute treatment sessions and up to 5 booster sessions.
Study Details
This research study plans to examine the use of Augmented Depression Therapy (ADepT) in order to evaluate what patients think about ADepT and how well it works. ADepT is a type of therapy that builds wellbeing and is being provided to you as standard of care. ADepT treatment consists of 15 therapy sessions (typically provided weekly) with each session lasting around 60 minutes. Following these sessions, you can receive five optional booster sessions over the next 12 months with each of these lasting around 60 minutes. Ultimately, the timing and duration of these sessions will be determined between you and your provider and scheduled accordingly. As part of this study you will be randomized (randomly assigned) to different research assessment lengths before the start of treatment and then will complete assessments for the 12 months following the end of the weekly portion of ADepT treatment. The length of your participation will be between 70 weeks to 82 weeks.
Key Dates
- First listed
- Jul 29, 2026
- Start date
- Aug 1, 2026
- Status verified
- Jul 2026
- Primary completion
- Aug 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: 3 week baseline + ADepTBaseline assessments will be made weekly for 3 weeks, followed by a standard course of ADepT.
- Experimental: 4 week baseline + ADepTBaseline assessments will be made weekly for 4 weeks, followed by a standard course of ADepT.
- Experimental: 5 week baseline + ADepTBaseline assessments will be made weekly for 5 weeks, followed by a standard course of ADepT.
- Experimental: 6 week baseline + ADepTBaseline assessments will be made weekly for 6 weeks, followed by a standard course of ADepT.
- Experimental: 7 week baseline + ADepTBaseline assessments will be made weekly for 7 weeks, followed by a standard course of ADepT.
- Experimental: 8 week baseline + ADepTBaseline assessments will be made weekly for 8 weeks, followed by a standard course of ADepT.
Primary Outcome Measure
Acceptability [ Time Frame: From enrollment to the end of treatment at 82 weeks ]
Central Contacts
- Jay Fournier, Ph.D.614-814-6485
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The Ohio State University Wexner Medical Center | Columbus | Ohio | 43214 |
Find similar trials in Columbus, OH
Related Studies
- Neural Correlates of Suicidal Behavior in YouthNot Yet Recruiting · The Cleveland Clinic · Cleveland, Ohio
- Youth Suicide Prevention: CAMS-BI vs. Safety Planning in a Randomized TrialNot Yet Recruiting · The Cleveland Clinic · Cleveland, Ohio
- Lumateperone for Late-Life DepressionPHASE3 · Not Yet Recruiting · Eric Lenze · Tucson, Arizona
- Intern Health Study 2026Enrolling By Invitation · University of Michigan · Ann Arbor, Michigan