Imagery Rescripting for Posttraumatic Nightmares in Rural Operation Enduring Freedom (OEF)/Operation Iraqi Freedom (OIF) Veterans With Posttraumatic Stress Disorder (PTSD)

NCT ID: NCT00837382

Last Updated: 2010-09-29

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 7 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-01-31
• Study Completion Date: 2010-08-31

Brief Summary

Many service members returning from Iraq and Afghanistan have difficulties adjusting back to civilian life. Research shows that symptoms of posttraumatic stress disorder (PTSD) are particularly high in returning Operation Enduring Freedom (OEF)/Operation Iraqi Freedom (OIF) veterans, and that combat-related nightmares and sleep disturbances are common in veterans with PTSD. This is of concern because people with these problems will often use unhealthy ways of coping. Although combat-related nightmares and difficulty sleeping are highly distressing, there are helpful treatments that do not involve taking medication. One of these treatments teaches specific skills to help people improve their sleep habits and to change their nightmares so that they are less upsetting. This treatment can be very helpful and research shows that people experience decreases in the frequency and severity of their nightmares, decreased symptoms of depression and PTSD, and improved sleep quality and quantity after completing treatment. However, because this treatment has only been studied with civilians, it is not clear how well this treatment works for returning veterans. This study tests how well this treatment works in treating combat nightmares in veterans who also have PTSD from experiencing a traumatic event.

Conditions

Stress Disorders, Post-Traumatic; Sleep Disorders

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

1

MEDVAMC Nightmare Treatment

Group Type: EXPERIMENTAL

MEDVAMC Nightmare Treatment

Intervention Type: BEHAVIORAL

Veteran Nightmare Treatment Using Imagery Rescripting

2

Videoconferencing nightmare Treatment

Group Type: EXPERIMENTAL

Telepsychiatry Nightmare Treatment

Intervention Type: BEHAVIORAL

Veteran Nightmare Treatment Using Imagery Rescripting Through Videoconferencing

Interventions

MEDVAMC Nightmare Treatment

Veteran Nightmare Treatment Using Imagery Rescripting

Intervention Type: BEHAVIORAL

Telepsychiatry Nightmare Treatment

Veteran Nightmare Treatment Using Imagery Rescripting Through Videoconferencing

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

Patients for the open trial will be

1. OEF/OIF veterans (aged 18-64);

2. English-speaking;

3. currently enrolled in the Trauma Recovery Program (TRP) at the Michael E. DeBakey Veteran Affairs Medical Center (MEDVAMC);

4. reporting at least one combat or war zone associated PTNM in the past week;

5. have an existing PTSD International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM); and

6. consenting to be in an open trial for treatment of PTNM. In addition, patients must agree to allow their assessment and therapy sessions to be video/audiotaped for the purposes of supervision.

Pilot Study: Patients for the pilot study will be

1. OEF/OIF veterans (aged 18-64);

2. English-speaking;

3. currently enrolled in the Conroe CBOC for their primary or mental health care;

4. reporting at least one combat or war zone associated PTNM in the past week;

5. have an existing PTSD ICD-9-CM diagnosis; and

6. consenting to be in the pilot study for treatment of PTNM. In addition, patients must agree to allow their assessment and therapy sessions to be video/audiotaped for the purposes of supervision.

Exclusion Criteria

Patients will be excluded for the following reasons:

1. current active suicidal/homicidal ideation and intent;

2. current substance dependence;

3. a diagnosis of bipolar or psychosis;

4. active participation in another psychosocial treatment for PTSD;

5. prescribed the medication Prazosin (a psychotropic medication for the treatment of nightmares).

Patients interested in receiving the intervention will not be excluded if they are taking psychotropic medication (except for Prazosin) and may continue to take their medication as prescribed throughout the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

US Department of Veterans Affairs

FED

Sponsor Role: lead

Responsible Party

Department of Veterans Affairs

Principal Investigators

Mary E. Long, PhD

Role: PRINCIPAL_INVESTIGATOR

Michael E. DeBakey VA Medical Center (152)

Locations

Michael E. DeBakey VA Medical Center (152)

Houston, Texas, United States

Countries

United States

Other Identifiers

H-24157

Identifier Type: -

Identifier Source: org_study_id