Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00837382 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by US Department of Veterans Affairs.

Terminated
Registry status
NA
Development phase
7
Enrollment target

NCT00837382: Clinical Trial NA study, sponsored by US Department of Veterans Affairs.

NCT00837382 is a NA study that was terminated before completion, run by US Department of Veterans Affairs. The registered enrollment target is 7 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00837382, a NA study, was terminated before completion, sponsored by US Department of Veterans Affairs.

TERMINATED
Registry status
NA
Development phase
7 participants
Enrollment target

Study 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.

Interventions

  • BEHAVIORAL MEDVAMC Nightmare Treatment
  • BEHAVIORAL Telepsychiatry Nightmare Treatment

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2010-01
Est. Completion 2010-08
Phase NA
US Department of Veterans Affairs

632 total trials

Why NCT00837382 stopped before completion

NCT00837382 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 2 interventions - of which MEDVAMC Nightmare Treatment is the first listed.

NCT00837382 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00837382 about?

NCT00837382 is a clinical study titled "Imagery Rescripting for Posttraumatic Nightmares in Rural Operation Enduring Freedom (OEF)/Operation Iraqi Freedom (OIF) Veterans With Posttraumatic Stress Disorder (PTSD)". 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...

What is the current status of trial NCT00837382?

This trial is currently terminated. It is a NA study. The enrollment target is 7 participants. The study started on 2010-01. Estimated completion is 2010-08.

What interventions are being tested in trial NCT00837382?

The interventions under investigation include: MEDVAMC Nightmare Treatment (BEHAVIORAL), Telepsychiatry Nightmare Treatment (BEHAVIORAL).

Who is sponsoring clinical trial NCT00837382?

This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00837382's enrollment target sits among peer trials

7 1982nd of 2000 higher than 18 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00837382, the US trial registry maintained by the National Library of Medicine. NCT00837382 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.