Skip to content

Mind-Body Skills Groups for the Treatment of War Zone Stress in Military and Veteran Populations

A Randomized Controlled Study of Mind-Body Skills Groups for Treatment of War Zone Stress in Military and Veteran Populations

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01093053
Enrollment
108
Registered
2010-03-25
Start date
2010-09-30
Completion date
2013-09-30
Last updated
2014-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anger, Anxiety Disorders, Brain Injuries, Depressive Disorder, Stress Disorders, Post Traumatic

Keywords

Mind-Body Therapies

Brief 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).

Detailed 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.

Interventions

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.

OTHERStandard 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.

Sponsors

U.S. Army Medical Research and Development Command
CollaboratorFED
Southeast Louisiana Veterans Health Care System
CollaboratorFED
The Center for Mind-Body Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
PTSD checklist - military versionBaseline; 12 weeks; 20 weeksThe PTSD checklist contains 17 items corresponding to the DSM-IV criteria for PTSD. Past month symptom severity is indicated using a 5 point scale.

Secondary

MeasureTime frameDescription
The Pittsburgh Sleep Quality IndexBaseline;12 weeks; 20 weeksThis 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.
The Patient Health Questionnaire-9Baseline;12 weeks; 20 weeksThe Patient Health Questionnaire-9 is a 9 item self-report measure and is a widely used screening tool for depression.
State-Trait Anxiety InventoryBaseline; 12 weeks; 20 weeksThe State anxiety subscale will be used. It has 20 questions and uses a 4 point scale.
State-Trait Anger Expression Inventory-2Baseline;12 weeks; 20 weeksThis 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)
The Medical Outcomes Study Short Form SF-36Baseline; 12 weeks; 20 weeksThe 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.
The Inventory of Functional ImpairmentBaseline;12 weeks; 20 weeksThe 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.
The Posttraumatic Growth InventoryBaseline;12 weeks; 20 weeksThe 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026