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Comparison of Two Treatments for Post-Traumatic Stress Disorder

Primary Purpose

Post-Traumatic Stress Disorder

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Sertraline
Cognitive behavioral therapy (CBT)
Sponsored by
Case Western Reserve University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-Traumatic Stress Disorder focused on measuring Antidepressants, Cognitive behavior therapy

Eligibility Criteria

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

Inclusion Criteria: DSM-IV diagnosis of PTSD Experienced traumatic event at least 12 weeks prior to study entry Willingness to discontinue current CBT or antidepressant treatment Exclusion Criteria: Current diagnosis of schizophrenia or delusional disorder Medically unstable bipolar disorder, depression with psychotic features, or depression requiring psychiatric treatment 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 either CBT or sertraline Medical contraindication for sertraline

Sites / Locations

  • Department of Psychology, 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

CBT no choice

CBT choice

sertraline no choice

sertraline choice

Arm Description

Participants will receive no choice cognitive behavioral therapy (CBT no choice)

Participants will receive choice cognitive behavioral therapy (CBT choice)

Participants will receive no choice sertraline (sertraline no choice)

Participants will receive choice sertraline (sertraline choice)

Outcomes

Primary Outcome Measures

PTSD Symptoms
total score, range from 0-80, higher scores are more severe
Depression Symptoms
Hamilton Depression Rating Scale (HAMD), total score, scoring range 0-50, with higher scores more severe depression
State Anxiety
State-Trait Anxiety Inventory - State version, total score, scoring range, 0-63, with higher scores more severe

Secondary Outcome Measures

Quality of Life Functioning
Sheehan Disability Scale (SDS), total score, scoring range 0-30 , higher scores indicative of worse functional impairment

Full Information

First Posted
August 5, 2005
Last Updated
April 28, 2022
Sponsor
Case Western Reserve University
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00127673
Brief Title
Comparison of Two Treatments for Post-Traumatic Stress Disorder
Official Title
Effectiveness of PTSD Treatment: CBT Versus Sertraline
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
September 2004 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
August 2011 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will compare the short- and long-term effectiveness of two different treatments for people with post-traumatic stress disorder.
Detailed Description
Exposure to traumatic events, such as automobile accidents and 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 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 CBT and the antidepressant sertraline. Participants will either be randomly assigned to CBT or sertraline, or they will be able to choose one of the two treatments, which will be given for 10 weeks, followed by 24 months of follow-up assessments. Participants in the CBT 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 antidepressant group will take sertraline daily for 10 weeks. These participants will be seen weekly 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 antidepressant 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 24 months. Participants who do not respond to their assigned or chosen treatment will be offered 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, 12, and 24 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
Post-Traumatic Stress Disorder
Keywords
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
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CBT no choice
Arm Type
Active Comparator
Arm Description
Participants will receive no choice cognitive behavioral therapy (CBT no choice)
Arm Title
CBT choice
Arm Type
Active Comparator
Arm Description
Participants will receive choice cognitive behavioral therapy (CBT choice)
Arm Title
sertraline no choice
Arm Type
Active Comparator
Arm Description
Participants will receive no choice sertraline (sertraline no choice)
Arm Title
sertraline choice
Arm Type
Active Comparator
Arm Description
Participants will receive choice sertraline (sertraline choice)
Intervention Type
Drug
Intervention Name(s)
Sertraline
Other Intervention Name(s)
Zoloft
Intervention Description
The dose of sertraline will be up to 200 mg daily for 10 weeks. There will also be weekly meetings with study psychiatrist.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive behavioral therapy (CBT)
Other Intervention Name(s)
Prolonged exposure (PE)
Intervention Description
CBT will include 10 weekly sessions of individual cognitive behavioral therapy.
Primary Outcome Measure Information:
Title
PTSD Symptoms
Description
total score, range from 0-80, higher scores are more severe
Time Frame
Post-treatment, ten weeks
Title
Depression Symptoms
Description
Hamilton Depression Rating Scale (HAMD), total score, scoring range 0-50, with higher scores more severe depression
Time Frame
Measured at Post-Treatment, at 10 weeks
Title
State Anxiety
Description
State-Trait Anxiety Inventory - State version, total score, scoring range, 0-63, with higher scores more severe
Time Frame
Measured at Post-Treatment, at 10 weeks
Secondary Outcome Measure Information:
Title
Quality of Life Functioning
Description
Sheehan Disability Scale (SDS), total score, scoring range 0-30 , higher scores indicative of worse functional impairment
Time Frame
Measured at Post-Treatment, at 10 weeks

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 diagnosis of PTSD Experienced traumatic event at least 12 weeks prior to study entry Willingness to discontinue current CBT or antidepressant treatment Exclusion Criteria: Current diagnosis of schizophrenia or delusional disorder Medically unstable bipolar disorder, depression with psychotic features, or depression requiring psychiatric treatment 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 either CBT or sertraline Medical contraindication for sertraline
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Norah C. Feeny, PhD
Organizational Affiliation
Department of Psychology, Case Western Reserve University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lori A. Zoellner, PhD
Organizational Affiliation
Department of Psychology, University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Psychology, 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
PubMed Identifier
32662191
Citation
Graham B, Garcia NM, Bergman HE, Feeny NC, Zoellner LA. Prolonged Exposure and Sertraline Treatments for Posttraumatic Stress Disorder Also Improve Multiple Indicators of Social Functioning. J Trauma Stress. 2020 Aug;33(4):488-499. doi: 10.1002/jts.22570. Epub 2020 Jul 13.
Results Reference
derived
PubMed Identifier
30336702
Citation
Zoellner LA, Roy-Byrne PP, Mavissakalian M, Feeny NC. Doubly Randomized Preference Trial of Prolonged Exposure Versus Sertraline for Treatment of PTSD. Am J Psychiatry. 2019 Apr 1;176(4):287-296. doi: 10.1176/appi.ajp.2018.17090995. Epub 2018 Oct 19.
Results Reference
derived
PubMed Identifier
29541927
Citation
Le QA, Doctor JN, Zoellner LA, Feeny NC. Effects of treatment, choice, and preference on health-related quality-of-life outcomes in patients with posttraumatic stress disorder (PTSD). Qual Life Res. 2018 Jun;27(6):1555-1562. doi: 10.1007/s11136-018-1833-4. Epub 2018 Mar 14.
Results Reference
derived
PubMed Identifier
24717377
Citation
Le QA, Doctor JN, Zoellner LA, Feeny NC. Cost-effectiveness of prolonged exposure therapy versus pharmacotherapy and treatment choice in posttraumatic stress disorder (the Optimizing PTSD Treatment Trial): a doubly randomized preference trial. J Clin Psychiatry. 2014 Mar;75(3):222-30. doi: 10.4088/JCP.13m08719.
Results Reference
derived
PubMed Identifier
23587015
Citation
Le QA, Doctor JN, Zoellner LA, Feeny NC. Minimal clinically important differences for the EQ-5D and QWB-SA in Post-traumatic Stress Disorder (PTSD): results from a Doubly Randomized Preference Trial (DRPT). Health Qual Life Outcomes. 2013 Apr 12;11:59. doi: 10.1186/1477-7525-11-59.
Results Reference
derived
Links:
URL
http://faculty.washington.edu/zoellner/PTSDTx.htm
Description
Click here for more information about the effectiveness of CBT and sertraline for PTSD

Learn more about this trial

Comparison of Two Treatments for Post-Traumatic Stress Disorder

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