Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID06210711

Prevention of Posttraumatic Stress: A Randomized Controlled Trial of Brief Prolonged Exposure Therapy for Injured Individuals at Level I Trauma Centers

Led by Baylor Research Institute · Updated on 2026-02-11

300

Participants Needed

3

Research Sites

26 weeks

Total Duration

On this page

Sponsors

B

Baylor Research Institute

Lead Sponsor

F

Froedtert Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating whether a brief treatment method called Brief Prolonged Exposure Therapy (Brief PE) can help prevent posttraumatic stress disorder (PTSD) and other related issues following injury. This randomized controlled trial focuses on individuals admitted to Level I Trauma Centers and aims to reduce psychological distress such as PTSD symptoms, depression, anxiety, pain, and improve quality of life up to 6 months after injury. Participants are randomly assigned to one of two groups. One group receives standard clinical care (Treatment as Usual) provided at the trauma centers, which may include evaluations and follow-up therapy or medication but no trauma-focused therapy. The other group receives the same standard care plus three 60-minute sessions of Brief PE. This therapy involves education about trauma reactions, breathing exercises, repeated exposure to trauma memories and avoided situations, and discussion to challenge unrealistic beliefs. Homework assignments support ongoing practice between sessions. During the study, participants complete assessments at baseline and at 1, 2, 3, and 6 months after starting. These include interviews and questionnaires measuring PTSD symptoms, depression, anxiety, pain, and quality of life. Researchers will monitor these outcomes to assess the therapy's impact. The study lasts up to 6 months for each participant, with ongoing follow-up to track psychological and health changes after injury.

CONDITIONS

Brief Title

Trauma BPE Prolonged Exposure Therapy for Injured Individuals Admitted to a Level I Trauma Center

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Between the ages of 18 and 75 years old.
  • Admitted to Baylor University Medical Center at Dallas, Baylor Scott & White Medical Center at Temple, or Froedtert Hospital and the Medical College of Wisconsin Level I Trauma Center.
Not Eligible

You will not qualify if you...

  • Patients in police custody.
  • Patients not fluent in English.
  • Patients with severe cognitive impairment.
  • Patients who are acutely suicidal.
  • Patients with active psychosis or acute mental health crises that would interfere with participation in the study or therapy sessions.
  • Patients unable to provide informed consent or participate in therapy due to cognitive or psychiatric conditions not otherwise specified above. (This last exclusion is inferred from the original to clarify the cognitive impairment and psychosis criteria for patient understanding.)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 3 sessions over approximately 2 weeks

Participants in the experimental group receive three 60-minute sessions of Brief Prolonged Exposure Therapy in addition to standard clinical treatment. Participants in the control group receive standard clinical treatment only.

3 therapy sessions (in-person)

Follow-up

Duration - 6 months

Participants complete follow-up assessments to monitor PTSD symptoms and other health outcomes at multiple timepoints after baseline.

Follow-up visits at 1, 2, 3, and 6 months depending on group assignment

Trial Site Locations

Total: 3 locations

1

Baylor University Medical Center

Dallas, Texas, United States, 75246

Actively Recruiting

2

Baylor Scott & White Medical Center - Temple

Temple, Texas, United States, 76508

Actively Recruiting

3

Froedtert & Medical College of Wisconsin

Milwaukee, Wisconsin, United States, 53226

Actively Recruiting

Loading map...

Research Team

A

Alexis Evans, M.S

K

Kamiah Moss, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Similar Trials

A Mechanistic Trial of the Neurobiology of Extinction Learni...

Posttraumatic Stress Disorder

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here