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Effects of Narrative Writing Duration and Post-writing Processing Instructions on PTSD

Effects of Narrative Writing Duration and Post-writing Processing Instructions on PTSD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01773811
Enrollment
49
Registered
2013-01-23
Start date
2012-02-29
Completion date
2014-05-31
Last updated
2014-05-15

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

Conditions

Posttraumatic Stress Disorder (PTSD)

Keywords

Posttraumatic Stress Disorder (PTSD), Narrative Writing

Brief summary

The current study proposes to directly measure how processing after participating in written disclosure about a traumatic life event affects physical and psychological outcomes.

Detailed description

Previous research has established the potential for narrative writing about traumatic events to result in positive benefits for physical and psychological health. Research has also provided evidence that written disclosure may reduce post-traumatic stress disorder (PTSD) symptoms. Several mechanisms of action have been proposed to explain why written disclosure produces positive benefits, but all have focused on processes occurring during the writing session. It has been suggested, however, that additional processing may occur after the writing exercises are over, yet no research has studied the influence of this processing on outcomes. The current study proposes to directly measure how processing after participating in written disclosure affects physical and psychological outcomes.

Interventions

BEHAVIORALNarrative Writing: Trauma-Assigned

Individuals will be writing about their most traumatic life event for 3 consecutive days for 20 minutes each. Those in the assigned group will be given instructions and weekly reminders to continue to think about their most traumatic event.

BEHAVIORALNarrative Writing: Trauma-Spontaneous

Individuals will be writing about their most traumatic life event for 3 consecutive days for 20 minutes each. Those in the spontaneous group will be given no further instructions.

Sponsors

University of Mississippi, Oxford
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Experienced a traumatic life event (DSM-IV-TR Criterion A) * Currently experiencing clinically significant levels of PTSD symptoms

Exclusion criteria

* Currently receiving psychotherapy * On medication that is not stable (i.e. medication has been changed within the past 6 weeks)

Design outcomes

Primary

MeasureTime frame
Level of PTSD symptoms as measured by the Clinician Administered PTSD Scale1 month after final writing session

Secondary

MeasureTime frameDescription
Physical health1 month after final writing sessionPhysical health as measured by the Pennebaker Inventory of Limibic Languidness (PILL)

Countries

United States

Outcome results

None listed

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