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Optimizing Posttraumatic Stress Disorder Treatment: Prolonged Exposure (PE) Versus PE Plus Sertraline (OPT)

Primary Purpose

Posttraumatic Stress Disorder

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Prolonged exposure (PE)
PE plus Sertraline
Sponsored by
Case Western Reserve University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Posttraumatic Stress Disorder focused on measuring PTSD, Antidepressants, Cognitive behavior therapy

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • DSM-IV (Diagnostic & Statistical Manual of Mental Disorders) diagnosis of PTSD (with severity threshold)
  • Experienced traumatic event at least 12 weeks prior to study entry
  • Willingness to discontinue current CBT or antidepressant treatment if needed

Exclusion Criteria:

  • Current diagnosis of schizophrenia or delusional disorder
  • Medically unstable bipolar disorder, depression with psychotic features, or depression requiring immediate psychiatric treatment
  • No clear trauma memory or trauma before age 3
  • Current diagnosis of alcohol or substance dependence within 3 months prior to study entry
  • Ongoing intimate relationship with the perpetrator of the traumatic event
  • History of nonresponse to adequate trial of either CBT or sertraline
  • Medical contraindication for sertraline
  • Current high dose use of benzodiazepines
  • Pregnant or sexually active female without adequate birth control

Sites / Locations

  • Psychological Sciences Department Case Western Reserve University
  • Psychology Department of University of Washington

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Choice: Prolonged exposure (PE)

Choice: PE plus sertraline

No choice: Prolonged exposure (PE)

No Choice: PE plus sertraline

Arm Description

Participants randomized to "choice" who choose prolonged exposure (PE).

Participants randomized to "choice" who choose PE plus sertraline.

Participants randomized to "no choice" who are then randomized to PE.

Participants randomized to "no choice" who are then randomized to PE plus sertraline.

Outcomes

Primary Outcome Measures

Posttraumatic stress disorder (PTSD) Symptoms
Interview measure to assess PTSD symptoms.

Secondary Outcome Measures

Depression symptoms
Clinical assessment of depression symptoms.

Full Information

First Posted
May 11, 2012
Last Updated
August 2, 2021
Sponsor
Case Western Reserve University
Collaborators
University of Washington, National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT01600456
Brief Title
Optimizing Posttraumatic Stress Disorder Treatment: Prolonged Exposure (PE) Versus PE Plus Sertraline
Acronym
OPT
Official Title
Optimizing PTSD Treatment: PE Versus PE Plus Sertraline
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
January 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Case Western Reserve University
Collaborators
University of Washington, National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The specific aims of this study are: To compare the effectiveness of a cognitive behavioral therapy (prolonged exposure, PE) to that of PE and medication (sertraline). To compare the durability of PE gains to that of PE and sertraline at 3, 6, and 9 months post-treatment. To compare those who have chosen their treatment to those who have not in terms of completion of treatment, treatment satisfaction, and short- and long-term effectiveness of the treatment. To examine cost effectiveness of treatment delivery to trauma survivors with PTSD.
Detailed Description
Exposure to traumatic events, such as automobile accidents and physical or sexual assault, can cause individuals to develop persistent psychological difficulties such as post-traumatic stress disorder (PTSD). PTSD is an anxiety disorder characterized by avoidance, hyperarousal symptoms, and mental re-experiencing of the traumatic event. PTSD is a serious condition that may cause social and psychological impairment; therefore, safe and effective treatments are needed. Both CBT (cognitive behavior therapy) and antidepressant therapy have been shown to effectively treat PTSD symptoms; however, comparisons of the treatments are limited. This study will compare the short- and long-term effectiveness of prolonged exposure and prolonged exposure plus the antidepressant sertraline. Participants will either be randomly assigned to prolonged exposure (PE) or PE plus sertraline, or they will be able to choose one of the two treatments,which will be given for 10 weeks, followed by 9 months of follow-up assessments. Participants in the PE group will have 10 weekly sessions of therapy. During the therapy sessions, participants will be encouraged to confront their general fears and the memory of their trauma through repeated storytelling. Participants will also be encouraged to practice the techniques learned in therapy in everyday life. Participants in the PE plus sertraline group receive the same treatment as the PE group plus they will take sertraline daily for 10 weeks. These participants will be seen regularly by a psychiatrist who will offer general encouragement and support, monitor response to medication, and record any side effects participants may be experiencing. The medication may be adjusted according to a dosing schedule and based on the study doctor's judgment. At the end of 10 weeks, participants in the PE plus sertraline group will have the choice of either tapering the medication gradually to minimize the chance of withdrawal symptoms or staying on the medication for up to 9 months. Participants who do not respond to their assigned or chosen treatment will be offered booster sessions or the other treatment for 10 weeks. Self-report scales and questionnaires will be used to assess participants' PTSD symptoms, depression, anxiety, and social functioning. These assessments will occur at 3, 6, and 9 months after the study treatment period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic Stress Disorder
Keywords
PTSD, Antidepressants, Cognitive behavior therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Choice: Prolonged exposure (PE)
Arm Type
Active Comparator
Arm Description
Participants randomized to "choice" who choose prolonged exposure (PE).
Arm Title
Choice: PE plus sertraline
Arm Type
Active Comparator
Arm Description
Participants randomized to "choice" who choose PE plus sertraline.
Arm Title
No choice: Prolonged exposure (PE)
Arm Type
Active Comparator
Arm Description
Participants randomized to "no choice" who are then randomized to PE.
Arm Title
No Choice: PE plus sertraline
Arm Type
Active Comparator
Arm Description
Participants randomized to "no choice" who are then randomized to PE plus sertraline.
Intervention Type
Behavioral
Intervention Name(s)
Prolonged exposure (PE)
Intervention Description
PE will include 10 weekly sessions of individual cognitive behavioral therapy.
Intervention Type
Other
Intervention Name(s)
PE plus Sertraline
Other Intervention Name(s)
Zoloft
Intervention Description
PE plus sertraline will include 10 weeks of prolonged exposure therapy plus sertraline. The sertraline dose will be up to 200 mg daily for 10 weeks. There will also be frequent meetings with study psychiatrist. PE will be provided 1x weekly for 10 weeks.
Primary Outcome Measure Information:
Title
Posttraumatic stress disorder (PTSD) Symptoms
Description
Interview measure to assess PTSD symptoms.
Time Frame
Measured up to 9 months.
Secondary Outcome Measure Information:
Title
Depression symptoms
Description
Clinical assessment of depression symptoms.
Time Frame
Measured up to 9 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: DSM-IV (Diagnostic & Statistical Manual of Mental Disorders) diagnosis of PTSD (with severity threshold) Experienced traumatic event at least 12 weeks prior to study entry Willingness to discontinue current CBT or antidepressant treatment if needed Exclusion Criteria: Current diagnosis of schizophrenia or delusional disorder Medically unstable bipolar disorder, depression with psychotic features, or depression requiring immediate psychiatric treatment No clear trauma memory or trauma before age 3 Current diagnosis of alcohol or substance dependence within 3 months prior to study entry Ongoing intimate relationship with the perpetrator of the traumatic event History of nonresponse to adequate trial of either CBT or sertraline Medical contraindication for sertraline Current high dose use of benzodiazepines Pregnant or sexually active female without adequate birth control
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Norah C Feeny, PhD
Organizational Affiliation
Case Western Reserve University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lori A Zoellner, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Psychological Sciences Department Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Psychology Department of University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
34672659
Citation
Rosencrans PL, Zoellner LA, Feeny NC. A network approach to posttraumatic stress disorder: Comparing interview and self-report networks. Psychol Trauma. 2021 Oct 21:10.1037/tra0001151. doi: 10.1037/tra0001151. Online ahead of print.
Results Reference
derived
Links:
URL
http://www.ptsdoptions.com
Description
Optimizing PTSD Treatment's Homepage

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Optimizing Posttraumatic Stress Disorder Treatment: Prolonged Exposure (PE) Versus PE Plus Sertraline

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