- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01607632
Loving-kindness Meditation for Posttraumatic Stress Disorder (PTSD)
May 24, 2012 updated by: David Kearney, Seattle Institute for Biomedical and Clinical Research
An Open Pilot Study of Loving-Kindness Meditation for PTSD
A before and after study of veterans who took part in a 12-week loving-kindness meditation course as an adjunct to their usual care for posttraumatic stress disorder.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
42
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Washington
-
Seattle, Washington, United States, 98108
- VA Puget Sound
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- posttraumatic stress disorder
Exclusion Criteria:
- psychosis
- borderline personality disorder
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: loving-kindness meditation
|
A 12-week duration, 90 minute per session loving-kindness meditation course
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change in PTSD symptoms
Time Frame: baseline, post-intervention, 3-month follow-up
|
The PTSD symptom-scale interview was performed
|
baseline, post-intervention, 3-month follow-up
|
change in depressive symptoms
Time Frame: baseline, post-intervention, 3-month follow-up
|
The PROMIS measure for depression was administered
|
baseline, post-intervention, 3-month follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: David Kearney, MD, VA Puget Sound
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2010
Primary Completion (Actual)
June 1, 2011
Study Completion (Actual)
June 1, 2011
Study Registration Dates
First Submitted
May 23, 2012
First Submitted That Met QC Criteria
May 24, 2012
First Posted (Estimate)
May 30, 2012
Study Record Updates
Last Update Posted (Estimate)
May 30, 2012
Last Update Submitted That Met QC Criteria
May 24, 2012
Last Verified
May 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 00173
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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