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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01093053
Other study ID # 08144040
Secondary ID
Status Completed
Phase N/A
First received March 24, 2010
Last updated January 27, 2014
Start date September 2010
Est. completion date September 2013

Study information

Verified date January 2014
Source The Center for Mind-Body Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether participation in mind-body skills groups by veterans who have experienced a stressful war-related situation and have symptoms of posttraumatic stress disorder (PTSD), will improve symptoms of PTSD, depression and anxiety, reduce anger, improve quality of life, quality of sleep and result in posttraumatic growth (a positive change that people can experience when they have been in a traumatic situation).


Description:

The study will be a randomized controlled study where participants will be randomly selected to either participate in the mind-body skills program and to answer questionnaires before and after the program and again 6 months later or, if they are not randomized to the mind-body skills group program, they will answer the questionnaires during the same time periods without participating in the program. Both groups will also continue their medical treatment as usual. The mind-body skills group intervention consists of groups of 8-10 participants. Two formats will be offered. (1) A 2 hour group session once a week for 10 weeks or (2) Weekend groups which will be run on alternating Saturdays, with a 2 hour session in the morning and another 2 hour session in the afternoon. The groups will be run for a total of 5 Saturday sessions. Additional "reunion" groups will be held at 1 month, 3 months, and 6 months in order to reinforce skills and to provide continuing social support.


Recruitment information / eligibility

Status Completed
Enrollment 108
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- having experienced a deployment-related criterion A stressor and reporting post deployment stress symptoms which include: clinically diagnosed posttraumatic stress disorder (PTSD), or subthreshold PTSD symptoms

- comorbid conditions may also include mild traumatic brain injury, or clinically significant levels of depression or anxiety.

Exclusion Criteria:

- current uncontrolled psychotic or bipolar disorder

- significant cognitive impairment

- moderate or severe TBI

- substance dependence

- suicidal or homicidal ideation

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Behavioral:
Mind-Body Skills Groups
The mind-body skills group program teaches participants how to do meditation, guided imagery, breathing techniques, and biofeedback. These mind-body techniques are taught and practiced in small groups of 8 to 10 people and also contain an element of social support.
Other:
Standard Treatment
May include individual or group psychotherapy consisting of cognitive behavioral therapy or present-centered (i.e. unrelated to mindfulness) psychotherapy as well as medication management. Medications for depression, anxiety, and sleep disorders are the most commonly used in standard treatment.

Locations

Country Name City State
United States Southeast Louisiana Veterans Healthcare System New Orleans Louisiana

Sponsors (3)

Lead Sponsor Collaborator
The Center for Mind-Body Medicine Southeast Louisiana Veterans Health Care System, U.S. Army Medical Research and Materiel Command

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary PTSD checklist - military version The PTSD checklist contains 17 items corresponding to the DSM-IV criteria for PTSD. Past month symptom severity is indicated using a 5 point scale. Baseline; 12 weeks; 20 weeks No
Secondary State-Trait Anger Expression Inventory-2 This is a 57 item consisting of a 4 point scale that measures the intensity of anger as an emotional state at a particular time (State Anger) and how often angry feelings are experienced over time as a personality trait (Trait Anger). There are 4 additional subscales which measure the outward expression of anger (Anger Expression-Out), holding or suppressing angry feelings (Anger Expression-In); controlling angry feelings by preventing the outward expression of anger (Anger Control-Out); and controlling anger feeling by calming down (Anger Control-In) Baseline;12 weeks; 20 weeks No
Secondary The Pittsburgh Sleep Quality Index This 9 item questionnaire using a 4 point scale measures seven areas of sleep: subjective sleep quality, sleep latency, sleep duration, habitual seep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction. Baseline;12 weeks; 20 weeks No
Secondary The Patient Health Questionnaire-9 The Patient Health Questionnaire-9 is a 9 item self-report measure and is a widely used screening tool for depression. Baseline;12 weeks; 20 weeks No
Secondary State-Trait Anxiety Inventory The State anxiety subscale will be used. It has 20 questions and uses a 4 point scale. Baseline; 12 weeks; 20 weeks No
Secondary The Posttraumatic Growth Inventory The Posttraumatic Growth Inventory measures positive change that people can experience when they have been in a traumatic situation. It is a 21 item self report scale that includes five subscales: relating to others, new possibilities, personal strength, spiritual challenge, and appreciation of life. Baseline;12 weeks; 20 weeks No
Secondary The Medical Outcomes Study Short Form SF-36 The SF-36 has 36 questions and measures functional status in eight dimensions: physical functioning, social functioning, role functioning-physical, role functioning-emotional, vitality, mental health, bodily pain, and general health perception. Baseline; 12 weeks; 20 weeks No
Secondary The Inventory of Functional Impairment The Inventory of Functional Impairment is an 87-item self-report measure designed to assess multiple dimensions of functional impairment experienced by active duty service members and veterans. Baseline;12 weeks; 20 weeks No
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