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A Randomized Controlled Trial of Meditation Compared to Exposure Therapy and Education Control on PTSD in Veterans

Primary Purpose

Post-traumatic Stress Disorder

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Transcendental Meditation
Prolonged Exposure
Educational control
Sponsored by
United States Department of Defense
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Post-traumatic Stress Disorder focused on measuring post-traumatic stress disorder, transcendental meditation, cognitive behavioral therapy, prolonged exposure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Current medical diagnosis of PTSD
  2. A symptom severity score of 45 or higher on the Clinically Administered PTSD Scale (CAPS)
  3. Three or more months since service-related trauma
  4. If being treated with psychoactive medication, a stable regimen (no change in drugs or dose) for at least 2 months before enrollment
  5. Age: 18 years or older
  6. Language: English literate -

Exclusion Criteria:

1. Current unstable or uncontrolled psychotic symptoms, mania or bipolar disorder 2. Current suicidal or homicidal ideation 3. Moderate or greater cognitive impairment indicated by chart diagnosis or observable cognitive difficulties 4. Having received Prolonged Exposure therapy or having been instructed in Transcendental Meditation.

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Sites / Locations

  • San Diego VA Healthcare System

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Transcendental Meditation

Prolonged Exposure

Educational Control

Arm Description

TM is a simple, natural, effortless mental technique practiced with eyes closed sitting for 20 minutes twice a day. This allows the practitioner to experience lesser excited levels of the mind and correspondingly greater degrees of physical relaxation. TM is a traditional meditation technique that has its origin in the ancient Vedic tradition of India.

Prolonged Exposure (PE) is a specialized type of Cognitive Behavorial Therapy employing a manualized, trauma-focused behavioral treatment for PTSD and is based on exposure principles and emotional processing theory.

Didactic based instructional classes will provide health education which will include the benefits of proper diet, exercise, and reducing smoking and alcohol. No stress management techniques will be taught.

Outcomes

Primary Outcome Measures

Clinically Administered PTSD Scale (CAPS)
This scale is currently the gold standard for assessing the severity of post-traumatic stress disorder (PTSD) using a face-to-face interview with the patient and a professionally trained medical/psychiatric administrator.

Secondary Outcome Measures

Self-Report Symptoms of PTSD
The PTSD Checklist- Military version (PCL-M) will assess PTSD symptoms in response to stressful military experiences. The Patient Health Questionnaire (PHQ)-9 will be used to evaluate clinical depression. The Profile of Mood States (POMS - will be used to evaluate total mood disturbance (TMD) main scale and tension/anxiety, depression/dejection, and anger/hostility subscales. The Social Support Questionnaire (SSQ) will be used to evaluate level of social support. The Quality of Life Enjoyment and Satisfaction Questionnaire-Short Form will used to assess overall quality of life.

Full Information

First Posted
May 24, 2013
Last Updated
November 21, 2018
Sponsor
United States Department of Defense
Collaborators
San Diego Veterans Healthcare System, Maharishi University of Management Research Institute, University of California, San Diego
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1. Study Identification

Unique Protocol Identification Number
NCT01865123
Brief Title
A Randomized Controlled Trial of Meditation Compared to Exposure Therapy and Education Control on PTSD in Veterans
Official Title
A Randomized Controlled Trial of Meditation Compared to Exposure Therapy and Education Control on PTSD in Veterans
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
June 2013 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
United States Department of Defense
Collaborators
San Diego Veterans Healthcare System, Maharishi University of Management Research Institute, University of California, San Diego

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to compare the effectiveness of the Transcendental Meditation (TM) program to the more standard Cognitive Behavioral Therapy with Prolonged Exposure (CBT-PE) in treating posttraumatic stress disorder (PTSD) in war Veterans over a three month treatment period.
Detailed Description
Posttraumatic stress disorder (PTSD) is a common and debilitating anxiety condition that affects up to 20% of war Veterans. PTSD is often a chronic problem for Veterans, affecting reintegration into society, family and marital relationships, sleep, employment stability, substance abuse rates, and risk for depression and suicide, among other areas. Although several effective therapies exist to treat PTSD, research shows that up to half of patients completing these treatments continue to have elevated symptoms indicating the important need for developing additional treatment options. In the current trial, we propose to test one such new treatment, specifically a meditation practice known as Transcendental Meditation. The Transcendental Meditation (TM) program will be compared to one of the best and most standard of PTSD therapies (Prolonged Exposure therapy), and a educational control group. This study will recruit 210 War Veterans clinically diagnosed with PTSD from the San Diego VA Healthcare System over a 4 year study period. The intervention period will be 3 months. Study participants will be randomized equally to one of three study groups, either Transcendental Meditation (TM) or Cognitive Behavioral Therapy with Prolonged Exposure (CBT-PE) or Educational control group. The primary outcome will be scores on the Clinically Administered PTSD Scale (CAPS). Secondary outcomes will includes scores on PTSD symptoms including depression, anger, mood disturbance and quality of life. Behavioral or lifestyle factors will also be measured including smoking, alcohol, and non-described drug usage along with compliance with each treatment. Physiological markers of stress and disease risk will include cortisol, blood pressure, inflammatory markers and body mass. If successful, these research findings will serve to provide key data on the feasibility and efficacy of the TM program as an alternative therapy for PTSD. The results will serve to inform policy decisions on the study and application of standardized and validated stress reduction programs in veteran populations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-traumatic Stress Disorder
Keywords
post-traumatic stress disorder, transcendental meditation, cognitive behavioral therapy, prolonged exposure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Transcendental Meditation
Arm Type
Experimental
Arm Description
TM is a simple, natural, effortless mental technique practiced with eyes closed sitting for 20 minutes twice a day. This allows the practitioner to experience lesser excited levels of the mind and correspondingly greater degrees of physical relaxation. TM is a traditional meditation technique that has its origin in the ancient Vedic tradition of India.
Arm Title
Prolonged Exposure
Arm Type
Active Comparator
Arm Description
Prolonged Exposure (PE) is a specialized type of Cognitive Behavorial Therapy employing a manualized, trauma-focused behavioral treatment for PTSD and is based on exposure principles and emotional processing theory.
Arm Title
Educational Control
Arm Type
Placebo Comparator
Arm Description
Didactic based instructional classes will provide health education which will include the benefits of proper diet, exercise, and reducing smoking and alcohol. No stress management techniques will be taught.
Intervention Type
Behavioral
Intervention Name(s)
Transcendental Meditation
Other Intervention Name(s)
meditation, mantra meditation, stress management
Intervention Description
A standard 7 step course will be offered including an introductory and preparatory lectures, personal one-on-one instruction with a certified TM teacher followed by 3 consecutive days of classes on how to meditate correctly and effortlessly, how to understand mechanisms of stress release and sequential development to higher levels of human consciousness and enjoying ones full potential. Followup meetings will provide checking of TM practice, sharing of group experiences with the TM practice and knowledge to motivate and inspire continued regularity with the practice. The certified TM instructor will have experience with PTSD in this veteran population.
Intervention Type
Behavioral
Intervention Name(s)
Prolonged Exposure
Other Intervention Name(s)
Cognitive Behavioral Therapy
Intervention Description
Prolonged exposure therapy, a specific form of cognitive behavioral therapy, is considered the standard psychotherapy treatment for PTSD . The delivery of PE will be by a trained study therapist. There will be 16 individual sessions provided to each participant. Homework will include relaxation and breathing exercises and anxiety diaries.
Intervention Type
Behavioral
Intervention Name(s)
Educational control
Other Intervention Name(s)
Health Education
Intervention Description
This group will receive group-administered didactic health education specific to the PTSD veterans population. It will include emphasis on healthy lifestyle changes to promote more positive mental and physical health. The classes will be matched with the TM and PE interventions to control for time, instructor attention and other non-specific factors.
Primary Outcome Measure Information:
Title
Clinically Administered PTSD Scale (CAPS)
Description
This scale is currently the gold standard for assessing the severity of post-traumatic stress disorder (PTSD) using a face-to-face interview with the patient and a professionally trained medical/psychiatric administrator.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Self-Report Symptoms of PTSD
Description
The PTSD Checklist- Military version (PCL-M) will assess PTSD symptoms in response to stressful military experiences. The Patient Health Questionnaire (PHQ)-9 will be used to evaluate clinical depression. The Profile of Mood States (POMS - will be used to evaluate total mood disturbance (TMD) main scale and tension/anxiety, depression/dejection, and anger/hostility subscales. The Social Support Questionnaire (SSQ) will be used to evaluate level of social support. The Quality of Life Enjoyment and Satisfaction Questionnaire-Short Form will used to assess overall quality of life.
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Behavioral Measures
Description
For substance usage, participants will be evaluated by the Weekly Recall (WR) method on alcohol, non-prescribed drugs, and smoking
Time Frame
3 months
Title
Biomarkers of Stress
Description
Blood Pressure will be measured three times with a mercury sphygmomanometer after five minutes rest. Three readings will be taken one minute apart. The latter two will be averaged for clinic visit mean. Participants will complete a 24-hour urine collection for catecholamine levels as a marker of chronic sympathetic nervous system activation and cortisol as a marker for hypothalamic-pituitary-adrenal (HPA) axis activation. Inflammatory biomarkers relevant to PTSD and cardiovascular disease will be assayed including C-Reactive Protein(CRP), Tumor Necrosis Factor(TNF-a), and Interleukin-6(IL-6).
Time Frame
3 months
Title
Treatment Adherence
Description
Adherence with the study interventions will be assessed through multiple measures in the two study groups. Adherence with health education and the stress reduction practice will be measured by: 1) daily home practice logs; 2) basic and follow-up meetings attended; and 3) random phone calls to participants by staff to determine recent practice of participants' respective programs. The Patient Satisfaction Questionnaire will also be used to evaluate the TM and CBT-PE programs.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Current medical diagnosis of PTSD A symptom severity score of 45 or higher on the Clinically Administered PTSD Scale (CAPS) Three or more months since service-related trauma If being treated with psychoactive medication, a stable regimen (no change in drugs or dose) for at least 2 months before enrollment Age: 18 years or older Language: English literate - Exclusion Criteria: 1. Current unstable or uncontrolled psychotic symptoms, mania or bipolar disorder 2. Current suicidal or homicidal ideation 3. Moderate or greater cognitive impairment indicated by chart diagnosis or observable cognitive difficulties 4. Having received Prolonged Exposure therapy or having been instructed in Transcendental Meditation. -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sanford I Nidich, EdD
Organizational Affiliation
Maharishi University of Management Research Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thomas Rutledge, PhD
Organizational Affiliation
San Diego VA Healthcare System
Official's Role
Principal Investigator
Facility Information:
Facility Name
San Diego VA Healthcare System
City
La Jolla
State/Province
California
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
25066921
Citation
Rutledge T, Nidich S, Schneider RH, Mills PJ, Salerno J, Heppner P, Gomez MA, Gaylord-King C, Rainforth M. Design and rationale of a comparative effectiveness trial evaluating transcendental meditation against established therapies for PTSD. Contemp Clin Trials. 2014 Sep;39(1):50-6. doi: 10.1016/j.cct.2014.07.005. Epub 2014 Jul 25.
Results Reference
background
PubMed Identifier
30449712
Citation
Nidich S, Mills PJ, Rainforth M, Heppner P, Schneider RH, Rosenthal NE, Salerno J, Gaylord-King C, Rutledge T. Non-trauma-focused meditation versus exposure therapy in veterans with post-traumatic stress disorder: a randomised controlled trial. Lancet Psychiatry. 2018 Dec;5(12):975-986. doi: 10.1016/S2215-0366(18)30384-5. Epub 2018 Nov 15.
Results Reference
result

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A Randomized Controlled Trial of Meditation Compared to Exposure Therapy and Education Control on PTSD in Veterans

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