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NCT03384706 · ClinicalTrials.gov registry record · NA
A Comparison of CPT Versus ART Versus WL
A NA study of Posttraumatic Stress Disorder, sponsored by University of Cincinnati.
- Completed
- Registry status
- NA
- Development phase
- 187
- Enrollment target
- 2
- Study locations
NCT03384706 is a NA study of Posttraumatic Stress Disorder that has completed, run by University of Cincinnati. The registered enrollment target is 187 participants, above the 110-participant average among 117 other Posttraumatic Stress Disorder trials with a reported enrollment target (70% higher). The trial reports 2 study locations across 1 state.
The verdict
NCT03384706, a NA study of Posttraumatic Stress Disorder, has completed, sponsored by University of Cincinnati.
- COMPLETED
- Registry status
- NA
- Development phase
- 187 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this research study is to compare the effectiveness of two treatments for the symptoms of Posttraumatic Stress Disorder (PTSD) with a no therapy, wait-list control condition. The two treatments are Cognitive Processing Therapy (CPT) as compared to Accelerated Resolution Therapy (ART). Both have been found to be effective with veterans and civilians in prior studies but they have never been compared to one another. Participants will be 280 males and females ages 18 and older who meet criteria for PTSD (or subthreshold PTSD). PTSD is a condition that can occur after a trauma experience such as combat, sexual abuse, physical abuse, or natural disasters.
Conditions Studied
Interventions
- BEHAVIORAL Cognitive Processing Therapy (CPT)
- BEHAVIORAL Accelerated Resolution Therapy (ART)
Study Locations (2)
Ohio
- University of Cincinnati - Cincinnati
- Cincinnati VA Medical Center - Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 187 participants |
| Start Date | 2017-09-06 |
| Est. Completion | 2021-03-15 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03384706
The ClinicalTrials.gov registry entry for NCT03384706 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 187 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 110-participant average among 117 other Posttraumatic Stress Disorder trials with a reported enrollment target (70% higher). The listed sponsor is University of Cincinnati, which has 245 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Posttraumatic Stress Disorder appearing as the primary indexed condition, and to 2 interventions - of which Cognitive Processing Therapy (CPT) is the first listed.
NCT03384706 reports 2 study locations spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT03384706 about?
NCT03384706 is a clinical study titled "A Comparison of CPT Versus ART Versus WL". The purpose of this research study is to compare the effectiveness of two treatments for the symptoms of Posttraumatic Stress Disorder (PTSD) with a no therapy, wait-list control condition. The two treatments are Cognitive Processing Therapy (CPT) as compared to Accelerated Resolution Therapy (ART)....
What is the current status of trial NCT03384706?
This trial is currently completed. It is a NA study. The enrollment target is 187 participants. The study started on 2017-09-06. Estimated completion is 2021-03-15.
What conditions does trial NCT03384706 study?
This clinical trial studies the following conditions: Posttraumatic Stress Disorder.
What interventions are being tested in trial NCT03384706?
The interventions under investigation include: Cognitive Processing Therapy (CPT) (BEHAVIORAL), Accelerated Resolution Therapy (ART) (BEHAVIORAL).
Who is sponsoring clinical trial NCT03384706?
This trial is sponsored by University of Cincinnati, which has 245 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03384706 being conducted?
This trial has 2 study locations across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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