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NCT01619384 · ClinicalTrials.gov registry record · NA
Mindfulness-Based Stress Reduction and the Microbiome
A NA study of Posttraumatic Stress Disorder and Irritable Bowel Syndrome, sponsored by Seattle Institute for Biomedical and Clinical Research.
- Completed
- Registry status
- NA
- Development phase
- 55
- Enrollment target
- 1
- Study location
NCT01619384 is a NA study of Posttraumatic Stress Disorder and Irritable Bowel Syndrome that has completed, run by Seattle Institute for Biomedical and Clinical Research. The registered enrollment target is 55 participants, below the 111-participant average among 117 other Posttraumatic Stress Disorder trials with a reported enrollment target (50% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01619384, a NA study of Posttraumatic Stress Disorder and Irritable Bowel Syndrome, has completed, sponsored by Seattle Institute for Biomedical and Clinical Research.
- COMPLETED
- Registry status
- NA
- Development phase
- 55 participants
- Enrollment target
- 1
- Study location
Study Summary
This proposed study aims to determine whether decreasing stress levels in persons with posttraumatic stress disorder (PTSD) can lead to a change in the intestinal microbiota, assessed 8 weeks after enrollment.
Conditions Studied
Interventions
- BEHAVIORAL Mindfulness-Based Stress Reduction
Study Locations (1)
Washington
- VA Puget Sound - Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 55 participants |
| Start Date | 2010-07 |
| Est. Completion | 2013-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01619384
The ClinicalTrials.gov registry entry for NCT01619384 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 55 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 111-participant average among 117 other Posttraumatic Stress Disorder trials with a reported enrollment target (50% lower). The listed sponsor is Seattle Institute for Biomedical and Clinical Research, which has 43 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Posttraumatic Stress Disorder appearing as the primary indexed condition, and to 1 intervention - of which Mindfulness-Based Stress Reduction is the first listed.
NCT01619384 reports 1 study location spanning 1 distinct geographic area - top geographies include Washington.
Frequently Asked Questions
What is clinical trial NCT01619384 about?
NCT01619384 is a clinical study titled "Mindfulness-Based Stress Reduction and the Microbiome". This proposed study aims to determine whether decreasing stress levels in persons with posttraumatic stress disorder (PTSD) can lead to a change in the intestinal microbiota, assessed 8 weeks after enrollment.
What is the current status of trial NCT01619384?
This trial is currently completed. It is a NA study. The enrollment target is 55 participants. The study started on 2010-07. Estimated completion is 2013-12.
What conditions does trial NCT01619384 study?
This clinical trial studies the following conditions: Posttraumatic Stress Disorder, Irritable Bowel Syndrome.
What interventions are being tested in trial NCT01619384?
The interventions under investigation include: Mindfulness-Based Stress Reduction (BEHAVIORAL).
Who is sponsoring clinical trial NCT01619384?
This trial is sponsored by Seattle Institute for Biomedical and Clinical Research, which has 43 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01619384 being conducted?
This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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