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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01306136
Other study ID # 1300209
Secondary ID
Status Completed
Phase Phase 1
First received February 28, 2011
Last updated February 28, 2011
Start date November 2008
Est. completion date October 2010

Study information

Verified date February 2011
Source University of Puerto Rico
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this project is to examine the feasibility of a culturally adapted, manual based Prolonged Exposure therapy intervention for the treatment of Spanish-speaking Puerto Ricans with posttraumatic stress disorder


Description:

This project seeks to lay the foundation for an effectiveness trial that will lead to the advancement of treatments for PTSD among Spanish-speaking Latinos, particularly Puerto Ricans. This area of research is important in light of the limited treatment options currently available for Spanish-speakers with PTSD and the long-term negative consequences of this condition. Participants in this study are recruited by referral from mental health providers in a general health setting. Patients meeting criteria for enrollment will be randomly assigned to receive either Prolonged Exposure therapy or treatment as usual. Assessments for all participants will be collected at baseline, week 8, and week 16 after randomization.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date October 2010
Est. primary completion date March 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- diagnosis of PTSD

- CAPS score of at least 45

- 18 to 65 years old

- Spanish speaker

- competent to provide informed consent

Exclusion Criteria:

- history of bipolar disease, schizophrenia or psychotic disorder

- alcohol or drug abuse in the past three months

- moderate to severe traumatic brain injury

- applying for or receiving disability benefits

- clinically judged to have a high acute suicide risk

- life-threatening medical condition

- currently receiving psychotherapy for PTSD or changed psychotropic medication within 2 months of randomization

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Intervention

Behavioral:
Prolonged Exposure
15 psychotherapy sessions focused on helping clients overcome avoidance behaviors and emotionally process trauma-related memories
Usual care
Per usual care, patients are referred to a mental health provider within the health care setting.

Locations

Country Name City State
Puerto Rico University of Puerto Rico, Medical Sciences Campus San Juan

Sponsors (1)

Lead Sponsor Collaborator
University of Puerto Rico

Country where clinical trial is conducted

Puerto Rico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinician-Administered PTSD Scale The Clinician-Administered PTSD Scale is a semi-structured interview designed to assess posttraumatic stress disorder (PTSD) diagnostic status and symptom severity. Baseline, week 8, week 16 No
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