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

NCT01199107 · ClinicalTrials.gov registry record · Phase 3

Maximizing Treatment Outcome and Examining Sleep in Post-traumatic Stress Disorder (PTSD)

A Phase 3 study of Post Traumatic Stress Disorder, sponsored by Southern Methodist University.

Completed
Registry status
Phase 3
Development phase
9
Enrollment target
1
Study location

NCT01199107: Completed Phase 3 study of Post Traumatic Stress Disorder, sponsored by Southern Methodist University.

NCT01199107 is a Phase 3 study of Post Traumatic Stress Disorder that has completed, run by Southern Methodist University. The registered enrollment target is 9 participants, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01199107, a Phase 3 study of Post Traumatic Stress Disorder, has completed, sponsored by Southern Methodist University.

COMPLETED
Registry status
Phase 3
Development phase
9 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to examine the efficacy of exercise in comparison to wellness education to determine if they can improve the effects of prolonged exposure therapy (PE) in reducing symptoms of anxiety associated with Post-traumatic Stress Disorder (PTSD). In addition, the two strategies (i.e., exercise and wellness education) will be compared in terms of improvements in sleep as well as levels of brain-derived neurotrophic factor (BDNF). BDNF is a protein that helps to support the survival of existing neurons and stimulate the growth new neurons and synapses. BDNF is important to learning and memory in general and therefore may be associated with the learning and memory as it relates to PE and corresponding symptom PTSD improvement.

Primary Outcome

Self-report measure that assesses PTSD Symptoms. Will be assessed at each visit throughout the 3 month protocol.

Interventions

  • BEHAVIORAL Exercise
  • BEHAVIORAL Prolonged Exposure
  • BEHAVIORAL Wellness Intervention

Study Locations (1)

Texas

  • Southern Methodist University - Dallas

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2010-09
Est. Completion 2013-08
Phase Phase 3
Southern Methodist University

17 total trials

What the finished NCT01199107 record still lists

NCT01199107 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 3 interventions - of which Exercise is the first listed.

NCT01199107 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT01199107 about?

NCT01199107 is a clinical study titled "Maximizing Treatment Outcome and Examining Sleep in Post-traumatic Stress Disorder (PTSD)". The purpose of this study is to examine the efficacy of exercise in comparison to wellness education to determine if they can improve the effects of prolonged exposure therapy (PE) in reducing symptoms of anxiety associated with Post-traumatic Stress Disorder (PTSD). In addition, the two strategies ...

What is the current status of trial NCT01199107?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 9 participants. The study started on 2010-09. Estimated completion is 2013-08.

What conditions does trial NCT01199107 study?

This clinical trial studies the following conditions: Post Traumatic Stress Disorder.

What interventions are being tested in trial NCT01199107?

The interventions under investigation include: Exercise (BEHAVIORAL), Prolonged Exposure (BEHAVIORAL), Wellness Intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT01199107?

This trial is sponsored by Southern Methodist University, which has 17 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01199107 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Post Traumatic Stress Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01199107's enrollment target sits among peer trials

9 251st of 262 higher than 8 of 262 other Post Traumatic Stress Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder 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 NCT01199107, the US trial registry maintained by the National Library of Medicine. NCT01199107 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.