Could a 5-Session writing exercise ease PTSD in pregnant teens?
NCT ID NCT06771817
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tests whether a short, 5-session writing therapy called Written Exposure Therapy (WET) is practical and helpful for pregnant or postpartum adolescents and young adults (ages 15-24) with PTSD. The therapy involves writing about traumatic experiences with minimal therapist time, making it potentially useful in low-resource settings. The study will measure how many participants complete treatment and whether PTSD symptoms improve.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Written Exposure Therapy (WET) - a brief, 5-session writing-based therapy with minimal therapist involvement
- What this could lead to
- If successful, this could offer a simple, short-term therapy option for PTSD in pregnant and postpartum youth, especially in low-resource settings.
- What could go wrong
- This is a very small pilot study (30 participants) with no control group, so results may not be generalizable. It only tests feasibility, not proven effectiveness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2025
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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15 to 24 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Stated willingness to comply with all study procedures and availability for the duration of the study 2. Have been referred by a clinician to the study or receiving standard of care treatment for pregnancy or post-partum follow-up 3. Aged 15-24 at time of screening 4. Either have Gestational age \>12 weeks or be \<1 year postpartum at time of screening 5. Able and willing to provide informed consent if 18 years of age or above or the legal guardian must be able and willing to provide informed consent if participant is less than 18 years of age and participant willing and able to provide assent if less than 18 years of age 6. Able to read, write and speak in English and Spanish; if the participant is under age 18, parents must be able to understand spoken or written English or Spanish. 7. Have the ability to complete clinical evaluations and self-report measures. 8. Meet diagnostic or subthreshold criteria for PTSD. Exclusion Criteria: 1. Have any condition for which, in the opinion of the investigator or designee, study participation would not be in their best interest (including but not limited to cognitive impairment, unstable general medical condition, intoxication, active psychosis) or that could prevent, limit, or confound the protocol-specified assessments. 2. Have current mania, hypomania, or psychosis 3. Be at serious suicidal risk that cannot be managed in the outpatient setting 4. Pervasive or intellectual developmental disorder requiring substantial or very substantial support. 5. Currently receiving or having received course of exposure-based therapy (e.g. WET, PE, CPT, or TF-CBT) in the past six months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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UT Southwestern Center for Depression Research and Clinical Care
Dallas, Texas, 75247, United States
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