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Pilot Study of Exposure Therapy for Posttraumatic Stress Disorder

U

University of Puerto Rico (UPR)

Status and phase

Completed
Phase 1

Conditions

Posttraumatic Stress Disorder

Treatments

Behavioral: Prolonged Exposure
Behavioral: Usual care

Study type

Interventional

Funder types

Other

Identifiers

NCT01306136
1300209

Details and patient eligibility

About

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

Full 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.

Enrollment

14 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

14 participants in 2 patient groups

Prolonged Exposure
Experimental group
Treatment:
Behavioral: Prolonged Exposure
Usual care
Active Comparator group
Treatment:
Behavioral: Usual care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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