Loving-kindness Meditation for Posttraumatic Stress Disorder (PTSD)
Primary Purpose
Posttraumatic Stress Disorder
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
loving-kindness meditation
Sponsored by
About this trial
This is an interventional treatment trial for Posttraumatic Stress Disorder focused on measuring posttraumatic stress, depression
Eligibility Criteria
Inclusion Criteria:
- posttraumatic stress disorder
Exclusion Criteria:
- psychosis
- borderline personality disorder
Sites / Locations
- VA Puget Sound
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
loving-kindness meditation
Arm Description
Outcomes
Primary Outcome Measures
change in PTSD symptoms
The PTSD symptom-scale interview was performed
change in depressive symptoms
The PROMIS measure for depression was administered
Secondary Outcome Measures
Full Information
NCT ID
NCT01607632
First Posted
May 23, 2012
Last Updated
May 24, 2012
Sponsor
Seattle Institute for Biomedical and Clinical Research
1. Study Identification
Unique Protocol Identification Number
NCT01607632
Brief Title
Loving-kindness Meditation for Posttraumatic Stress Disorder (PTSD)
Official Title
An Open Pilot Study of Loving-Kindness Meditation for PTSD
Study Type
Interventional
2. Study Status
Record Verification Date
May 2012
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seattle Institute for Biomedical and Clinical Research
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic Stress Disorder
Keywords
posttraumatic stress, depression
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
42 (Actual)
8. Arms, Groups, and Interventions
Arm Title
loving-kindness meditation
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
loving-kindness meditation
Intervention Description
A 12-week duration, 90 minute per session loving-kindness meditation course
Primary Outcome Measure Information:
Title
change in PTSD symptoms
Description
The PTSD symptom-scale interview was performed
Time Frame
baseline, post-intervention, 3-month follow-up
Title
change in depressive symptoms
Description
The PROMIS measure for depression was administered
Time Frame
baseline, post-intervention, 3-month follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
posttraumatic stress disorder
Exclusion Criteria:
psychosis
borderline personality disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Kearney, MD
Organizational Affiliation
VA Puget Sound
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Puget Sound
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Loving-kindness Meditation for Posttraumatic Stress Disorder (PTSD)
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