PTSD Clinical Trial
Official title:
A Pilot Study of Big Mind for Veterans With PTSD
Verified date | April 2016 |
Source | VA Salt Lake City Health Care System |
Contact | n/a |
Is FDA regulated | No |
Health authority | Unspecified |
Study type | Interventional |
A variety of mindfulness-based interventions, such as Mindfulness-Based Stress Reduction and
Mindfulness-Based Cognitive Therapy have been shown to be beneficial for individuals
experiencing mood and anxiety symptoms. The aim of this pilot study is to test the
feasibility of using a similar intervention, known as Big Mind, for veterans with PTSD and
other psychological symptoms.
Big Mind is a method of self-exploration that utilizes a voice dialog technique to help
individuals see the world and themselves from a variety of perspectives. The investigators
hypothesize that this process will increase mindfulness and decrease self-referential
thinking, which is associated with negative affect.
To test the feasibility of using this method, veterans with PTSD will complete a four-week
group Big Mind class with a total of four sessions. The investigators will use a single
group design with pre and post-intervention measures to assess tolerability and acceptance
of the intervention. Secondary outcome measures will evaluate symptom improvement and
increased mindfulness.
If this project demonstrates that using this intervention for veterans with PTSD is
feasible, then more rigorous clinical trials will be warranted.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | April 2016 |
Est. primary completion date | April 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - male and female veterans with PTSD - age 18 - 65 - ability to provide informed consent Exclusion Criteria: - diagnosis of any psychotic disorder - psychotic symptoms secondary to a mood disorder or other condition - diagnosis of cognitive impairment or dementia - currently on facility suicide high-risk list - pregnancy - impaired decision-making capacity |
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | George E. Whalen VAMC | Salt Lake City | Utah |
Lead Sponsor | Collaborator |
---|---|
VA Salt Lake City Health Care System |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Feasibility | The investigators will assess tolerability and acceptance of the intervention via subjective feedback from each participant at the end of week 4, and monitor drop out rates. | 4 weeks | No |
Secondary | Improvement of PTSD symptoms | Improvement of PTSD symptoms will be measured via PCL-5 questionnaire. | 4 weeks | No |
Secondary | Increase in mindfulness | Increase in mindfulness will be measured via the Five Facet Mindfulness Questionnaire. | 4 weeks | No |
Secondary | Improvement of depressive symptoms | Improvement of depressive symptoms will be measured via HAM-D rating scale for depression. | 4 weeks | No |
Secondary | Improvement of anxiety | Improvement of anxiety will be measured via HAM-A rating scale for anxiety. | 4 weeks | No |
Secondary | Improvement of sleep | Improvement of sleep will be measured via Sleep Scale from the Medical Outcomes Study. | 4 weeks | No |
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