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Examining Written Disclosure as a Treatment for Post-Traumatic Stress Disorder

Examining Written Disclosure as an Intervention for Posttraumatic Stress Disorder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00862498
Enrollment
48
Registered
2009-03-17
Start date
2008-08-31
Completion date
2011-08-31
Last updated
2018-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-Traumatic Stress Disorder

Keywords

PTSD, Written Disclosure, Written Emotional Disclosure, Narrative Exposure, Narrative Writing, Motor Vehicle Accident

Brief summary

This study will test the effectiveness of writing about a traumatic incident to treat post-traumatic stress disorder in people who have been in car accidents.

Detailed description

Post-traumatic stress disorder (PTSD) is a chronic and debilitating disorder caused by experiencing a stressful or traumatic event. Although there is evidence that treatments for PTSD are effective, many people do not seek treatment or seek treatment only after their PTSD has become severe. This study will test a low-cost, brief, and easily implemented treatment that may encourage people to seek treatment for PTSD. The treatment, called written disclosure (WD), involves writing about the traumatic event that caused a person's PTSD. In this study, people who have PTSD as the result of a motor vehicle accident will test two versions of WD, one administered in a clinic and the other administered over the phone. Participation in this study will last 5 weeks, with follow-up assessments continuing until 6 months after treatment. After screening, participants will be assigned to one of three conditions: WD treatment delivered in the clinic, WD treatment delivered via phone, and waitlist. The WD treatment involves five weekly writing sessions. During the first session, trauma reactions and the rationale for WD will be explained to all participants, and then participants will write for 30 minutes about their motor vehicle accident. The next four sessions will involve only writing for 30 minutes. For those receiving treatment in the clinic, a therapist will communicate directions and explanations to participants, and participants will have their heart rate activity recorded continuously for 5 minutes prior to writing and during the 30 minutes of writing. For those receiving treatment over the phone, explanations of the study will be provided in writing, and a study staff member will call participants before and after each writing session to ensure that participants understand the directions and are not experiencing any unexpected negative reactions after writing. Participants in the waitlist condition will not receive treatment for the first 4 months. After that period, they will be offered the WD treatment. Assessments of all participants will occur at baseline, after treatment, and 3 months after treatment. Participants assigned to receive WD treatment, either in a clinic or via phone, will also be assessed 6 months after treatment. Assessments administered at these points will involve semi-structured clinical interviews, self-report questionnaires, and measures of mood-related symptoms. Participants receiving treatment will also complete self-report measurements of emotional response after each writing session and the Daily Experiences Questionnaire every day during the 5 weeks of treatment. Participants on the waitlist will also undergo assessments of suicidal thoughts and PTSD symptoms every 2 weeks.

Interventions

OTHERWritten Disclosure

Five sessions, each spaced 1 week apart, during which participants are asked to write about their motor vehicle accident for 30 minutes. The first session of the intervention also involves a description of common reactions to a motor vehicle accident and the rationale for this treatment.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Boston University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Primary diagnosis of post-traumatic stress disorder * Involved in motor vehicle accident that occurred at least 3 months ago

Exclusion criteria

* Current diagnosis of mania, hypomania, bipolar depression, psychotic disorder, substance abuse disorder, or severe depression * History of psychosis * Active suicidality or history of two or more suicide gestures or attempts in the past year * Significant cognitive impairment * Current participation in a psychosocial treatment, such as individual or group therapy led by a clinician

Design outcomes

Primary

MeasureTime frame
Clinician-Administered Posttraumatic Stress Disorder ScaleMeasured at baseline, post-treatment, and at 3- and 6-month follow-ups

Secondary

MeasureTime frame
Posttraumatic Cognitions InventoryMeasured at baseline, post-treatment, and at 3- and 6-month follow-ups
Anxious Driving QuestionnaireMeasured at baseline, post-treatment, and at 3- and 6-month follow-ups
Client Satisfaction QuestionnaireMeasured at the end of the last treatment session
Daily Experiences QuestionnaireMeasured every day during the 5-week treatment period
Oswestry Disability IndexMeasured at baseline, post-treatment, and at 3- and 6-month follow-ups
Beck Depression Inventory - Second EditionMeasured at baseline, post-treatment, and at 3- and 6-month follow-ups
Self-Assessment ManikinMeasured after each writing session
Last Day of Writing QuestionnaireMeasured after the last writing session
Follow-Up Writing QuestionnaireMeasured after the 3-month follow-up assessment
Alcohol Use Disorders Identification TestMeasured at baseline, post-treatment, and at 3- and 6-month follow-ups
Posttraumatic Stress Disorder Checklist - Civilian VersionMeasured at baseline, post-treatment, and at 3- and 6-month follow-ups
Quality of Life InventoryMeasured at baseline, post-treatment, and at 3- and 6-month follow-ups

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026