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Active, not recruiting Not applicable Interventional Accepts healthy volunteers

Building Experience for Treating Trauma and Enhancing Resilience (BETTER)

ClinicalTrials.gov ID: NCT05330442

Public ClinicalTrials.gov record NCT05330442. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 3:00 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Delivering Written Exposure Therapy for PTSD in Underserved Primary Care Settings

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Posttraumatic stress disorder (PTSD) is a significant problem among underserved populations who receive care in community health centers. Several evidence-based psychotherapies for PTSD are not practical given the time and resources required for these approaches. This research will examine whether Written Exposure Therapy (WET), a brief and well-tolerated therapy approach, delivered within collaborative primary care is effective and can be implemented successfully within a collaborative care (CC) intervention. The primary aims of the proposed study are to evaluate the effectiveness and implementation of delivering WET into CoCM to improve the management of PTSD among underserved primary care patients in Federally Qualified Health Centers (FQHCs).

Study identification

NCT ID
NCT05330442
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
RAND
Other
Enrollment
720 participants

Conditions and interventions

Conditions

Interventions

Behavioral

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 24, 2022
Primary completion
Jul 30, 2026
Completion
Jul 25, 2027
Last update posted
Aug 13, 2026

2022 – 2027

United States locations

U.S. sites
10
U.S. states
2
U.S. cities
6
Facility City State ZIP Site status
Oak Orchard Health Center (Albion) Albion New York 14411
Brownsville Health Center (Genesis and Ashford - BGA) Brooklyn New York 11212
Brownsville Health Center (Main) Brooklyn New York 11212
Bedford Stuyvesant Family Health Center (Main) Brooklyn New York 11216
Bedford Stuyvesant Family Health Center (Sterling and Broadway) Brooklyn New York 11216
Oak Orchard Health (Pembroke) Corfu New York 14036
Open Door Family Medical Center (Brewster/Ossining) Ossining New York 10562
Open Door Family Medical Center (Mamaroneck//Port Chester) Port Chester New York 10573
OIC Family Medical Center (Fairview) Rocky Mount North Carolina 27801
OIC Family Medical Center (Happy Hill) Rocky Mount North Carolina 27804

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05330442, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 13, 2026 · Synced Sep 2, 2026

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The complete protocol, eligibility criteria, and contact information for NCT05330442 live on ClinicalTrials.gov.

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