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Stress-Reducing Interventions in HIV+ Patients: Pilot (PEACH)

Kent State University logo

Kent State University

Status

Unknown

Conditions

Stress Disorders, Post-Traumatic
HIV Infections

Treatments

Behavioral: Prolonged Exposure Therapy

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00599599
R34MH071201-01A1
NIMH, 1 R34 MH071201-01A1

Details and patient eligibility

About

The primary aim of this project is to examine the efficacy of prolonged exposure (PE) therapy at reducing HIV-related PTSD symptoms, increasing adherence to antiretroviral medication regimens, and increasing health-related quality of life (QOL) in HIV+ patients.

Full description

HIV+ patients will be randomized to receive either PE therapy (up to 18 possible sessions) or weekly symptom monitoring (described below) and will complete measures of PTSD, adherence, and QOL pre- and post-intervention and at 3- and 6-month follow-up assessments. Secondary analyses will examine the impact of the intervention on disorders commonly comorbid with PTSD (i.e., anxiety, mood, and substance abuse/dependence disorders).

Enrollment

70 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Must be HIV+
  • Must meet PTSD diagnostic criteria
  • Must be taking HIV medications
  • Must be able to read and write in English

Exclusion criteria

  • Current or previous diagnosis of schizophrenia, any current diagnosis with psychotic features, or current suicidal ideation
  • Being in a current abusive relationship or ongoing intimate relationship with one's assailant
  • Mental retardation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

1
Experimental group
Description:
Prolonged Exposure Therapy.
Treatment:
Behavioral: Prolonged Exposure Therapy
2
No Intervention group
Description:
Weekly monitoring/Waitlist Control Group.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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