- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01628809
Mindfulness-Based Meditation to Treat Stress in Unemployed Community Adults
Stress Reduction and Healthy Living in Pittsburgh
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Chronic stress has been shown to be a significant risk factor for increased morbidity and mortality. Eight-week Mindfulness-Based Meditation programs (MBSR) have been shown to improve participants' health and well-being, including reducing inflammation and slowing the progression of chronic diseases such as HIV. The purpose of this study is to evaluate the potential benefits of a three-day mindfulness-based meditation retreat program (vs. an active rest and relaxation retreat control condition) on a highly stressed, unemployed, community adult population.
Participants are recruited from the Pittsburgh area and are randomly assigned to either the mindfulness-based retreat program or the rest and relaxation retreat program. All participants complete a psychosocial survey, blood work, and a baseline fMRI before completing the intervention. Participants complete a second fMRI immediately following the intervention and then additional blood work and psychosocial surveys at a four month follow-up timepoint. At each fMRI appointment, participants will complete neuroimaging tasks (where they will be presented with words, picture, and sounds) that will assess neuroreactivity, regulation responses, and brain volume before and after mindfulness meditation training.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- English-speaking adults between the ages of 24 and 52 years at time of entry
- non-pregnant women only
- currently unemployed
- high levels of self-reported stress
- geographically accessible and willing to travel to and attend all study sessions
Exclusion Criteria:
- not able to attend scheduled three-day retreat
- have regularly (>1 time per week) practiced a mind-body therapy anytime in the last six months (e.g., meditation, yoga, tai chi)
- indicate any major physical health problems in the last six months
- have more than 15 alcoholic drinks in the average week
- have been diagnosed with a chronic disease (e.g. HIV, diabetes, arthritis)
- use medications affecting cardiovascular or endocrine function
- are left-handed
- have metal in their bodies (including pacemakers and permanent piercings (e.g., bellyrings, but not dental fillings))
- indicate regular use of psychotropic medication or psychotherapy in the last six months
- cognitive impairment as indicated by a score lower than 23 on the Mini-Mental State examination
- demonstrate low levels of stress due to unemployment
- smokers
- indicate use of recreational drugs in the past month
- indicate feeling claustrophobic in confined spaces, such as an fMRI scanner
- weigh over 350 lbs
- have any neurological disorders
- indicate any use of doctor prescribed cholesterol lowering medications (e.g., statins)
- currently employed
- not currently looking for a job
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Rest and Relaxation
three-day relaxation retreat without mindfulness components
|
three-day mindfulness-based meditation retreat program
Other Names:
|
|
Experimental: Mindfulness-Based Meditation
three-day mindfulness-based meditation retreat
|
three-day mindfulness-based meditation retreat program
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Neural Activity
Time Frame: Change from randomization to 1 week
|
Neural response to emotionally evocative stimuli including stressors related to be unemployed
|
Change from randomization to 1 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Brain volume
Time Frame: Change from randomization to 1 week
|
Change in volume of brain areas associated with emotional reactivity
|
Change from randomization to 1 week
|
|
Pro-inflammation
Time Frame: from baseline to four-month follow-up
|
Change in protein measures of inflammation
|
from baseline to four-month follow-up
|
|
Psychological Distress
Time Frame: baseline to four month follow-up
|
self-reported psychological distress
|
baseline to four month follow-up
|
|
Cortisol Levels
Time Frame: 1 day
|
Levels of cortisol were assessed from a small sample of participants' hair
|
1 day
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Taren AA, Gianaros PJ, Greco CM, Lindsay EK, Fairgrieve A, Brown KW, Rosen RK, Ferris JL, Julson E, Marsland AL, Creswell JD. Mindfulness Meditation Training and Executive Control Network Resting State Functional Connectivity: A Randomized Controlled Trial. Psychosom Med. 2017 Jul/Aug;79(6):674-683. doi: 10.1097/PSY.0000000000000466.
- Creswell JD, Taren AA, Lindsay EK, Greco CM, Gianaros PJ, Fairgrieve A, Marsland AL, Brown KW, Way BM, Rosen RK, Ferris JL. Alterations in Resting-State Functional Connectivity Link Mindfulness Meditation With Reduced Interleukin-6: A Randomized Controlled Trial. Biol Psychiatry. 2016 Jul 1;80(1):53-61. doi: 10.1016/j.biopsych.2016.01.008. Epub 2016 Jan 29.
- Taren AA, Gianaros PJ, Greco CM, Lindsay EK, Fairgrieve A, Brown KW, Rosen RK, Ferris JL, Julson E, Marsland AL, Bursley JK, Ramsburg J, Creswell JD. Mindfulness meditation training alters stress-related amygdala resting state functional connectivity: a randomized controlled trial. Soc Cogn Affect Neurosci. 2015 Dec;10(12):1758-68. doi: 10.1093/scan/nsv066. Epub 2015 Jun 5.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HLS-2011
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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