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OpenTrials
Completed

NCT Number: NCT00127673

Comparison of Two Treatments for Post-Traumatic Stress Disorder

This study will compare the short- and long-term effectiveness of two different treatments for people with post-traumatic stress disorder.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Department of Psychology, University of Washington

Seattle, Washington, 98195, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Sertraline

Drug

The dose of sertraline will be up to 200 mg daily for 10 weeks. There will also be weekly meetings with study psychiatrist.

Other names: Zoloft

Cognitive Behavioral Therapy (CBT)

Behavioral

CBT will include 10 weekly sessions of individual cognitive behavioral therapy.

Other names: Prolonged exposure (PE)

Primary outcomes

  1. PTSD Symptoms

    Time frame: Post-treatment, ten weeks

    total score, range from 0-80, higher scores are more severe

  2. Depression Symptoms

    Time frame: Measured at Post-Treatment, at 10 weeks

    Hamilton Depression Rating Scale (HAMD), total score, scoring range 0-50, with higher scores more severe depression

  3. State Anxiety

    Time frame: Measured at Post-Treatment, at 10 weeks

    State-Trait Anxiety Inventory - State version, total score, scoring range, 0-63, with higher scores more severe

Secondary outcomes

  1. Quality of Life Functioning

    Time frame: Measured at Post-Treatment, at 10 weeks

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

Sponsors and collaborators

Lead sponsor

Case Western Reserve University

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Effectiveness of PTSD Treatment: CBT Versus Sertraline

Important dates

Study start
2004
Primary completion
2011
Study completion
2011
First posted
Aug 8, 2005
Registry last updated
May 24, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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