Brief Internet Based Treatment for PTSD

Internet Based Treatment Using Virtual Reality in the Prevention of PTSD

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01760213

Enrollment

900

Registered

2013-01-04

Start date

2013-01-31

Completion date

2015-08-31

Last updated

2013-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

PTSD

Brief summary

The goal of the project is to overcome some of the common barriers to treatment amongst recent survivors of traumatic events, by combining the world of evidence-based intervention with that of modern Internet technology. Specifically, it aims to test the feasibility and effectiveness of an Internet delivery of early-intervention trauma-focused cognitive behavioral therapy (CBT) for preventing post-traumatic stress disorder (PTSD). Over the course of the study the following objectives will be achieved: 1. The development of an Internet-based Virtual Reality intervention for preventing PTSD among patients who have recently experienced a traumatic event. 2. The evaluation of the feasibility of administering this intervention, and 3. The evaluation of the efficacy of this Internet based intervention in the prevention of PTSD in recent trauma survivors.

Interventions

OTHERCBT delivered via Internet

Study design

Allocation

RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Inclusion criteria

* Exposed to a traumatic event that meets DSM Criteria (objectively could cause physical injury; * Subjectively involves helplessness or fear); * Aged over 18; Aged under 65; * Hebrew speaking; Suffering from PTSD (without the time criteria i.e. less than one month of symptoms); * Able to give informed consent.

Exclusion criteria

* Suffering from, or have suffered from in the past, bipolar disorder; * Suffering from, or have suffered from in the past, psychotic disorder; * Suffering from, or have suffered from in the past, substance abuse; * Suffering from PTSD; * Suffering from another Axis I anxiety disorder that requires immediate treatment; * Currently presents as a suicide risk, requiring hospitalization.

Design outcomes

Primary

Measure	Time frame	Description
Levels of PTSD symptoms	12 months after end of treatment	the main outcome measure will be PTSD symptoms as measured by the CAPS.

Countries

Israel

Contacts

Primary ContactRena Cooper, MD

crena@hadassah.org.il

Backup ContactSara Freedman, PhD

sarafreedman@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026