Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01911585 · ClinicalTrials.gov registry record · NA
Efficacy of 60-minute Versus 90-minute Sessions in Treating PTSD Using Prolonged Exposure
A NA study, sponsored by University of Pennsylvania.
- Completed
- Registry status
- NA
- Development phase
- 160
- Enrollment target
NCT01911585: Completed NA study, sponsored by University of Pennsylvania.
NCT01911585 is a NA study that has completed, run by University of Pennsylvania. The registered enrollment target is 160 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01911585, a NA study, has completed, sponsored by University of Pennsylvania.
- COMPLETED
- Registry status
- NA
- Development phase
- 160 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether 60-minute sessions of prolonged exposure (PE) are as effective as the standard 90-minute session for treating posttraumatic stress disorder (PTSD). Participants will include patients ages 18 or older with a current diagnosis of PTSD who are seeking treatment in our clinic. Patients who have current substance dependence, psychosis, and suicidal ideation with intent and plan may not be suitable for receiving PE and may be offered another treatment or referred to a different treatment center. Participants will be randomized to receive either the 90- minute or 60-minute PE session. A blind evaluator will assess for pre-treatment, post-treatment, and follow-up levels of symptom severity using the PTSD Symptoms Scale Interview (PSS-I). Participants will attend weekly treatment sessions with any of our faculty members and will complete self-report measures at every session (see below).
Interventions
- BEHAVIORAL Prolonged Exposure Therapy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 160 participants |
| Start Date | 2013-09 |
| Est. Completion | 2021-06-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01911585
The ClinicalTrials.gov registry entry for NCT01911585 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Prolonged Exposure Therapy is the first listed.
NCT01911585 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01911585 about?
NCT01911585 is a clinical study titled "Efficacy of 60-minute Versus 90-minute Sessions in Treating PTSD Using Prolonged Exposure". The purpose of this study is to determine whether 60-minute sessions of prolonged exposure (PE) are as effective as the standard 90-minute session for treating posttraumatic stress disorder (PTSD). Participants will include patients ages 18 or older with a current diagnosis of PTSD who are seeking t...
What is the current status of trial NCT01911585?
This trial is currently completed. It is a NA study. The enrollment target is 160 participants. The study started on 2013-09. Estimated completion is 2021-06-30.
What interventions are being tested in trial NCT01911585?
The interventions under investigation include: Prolonged Exposure Therapy (BEHAVIORAL).
Who is sponsoring clinical trial NCT01911585?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.