MIND: Mindfulness Meditation in Older Adults

Sponsor
University of California, Los Angeles (Other)
Overall Status
Completed
CT.gov ID
NCT01532596
Collaborator
(none)
40
1
2
12
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Study Details

Study Description

Brief Summary

The purpose of this study is to test if an 8-week mindfulness meditation training (vs a wait-list control condition) program reduces neurobehavioral reactivity and improves affect regulation in a sample of older adults, as measured by functional magnetic resonance imaging. Additionally, we will examine if mindfulness meditation training reduces loneliness and markers of chronic inflammation.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness-Based Stress Reduction
Early Phase 1

Detailed Description

It is well established that mindfulness meditation interventions improve a wide-range of mental and physical health outcomes in stressed patient populations, although the underlying mechanisms are currently unknown. It has been suggested that mindfulness training may reduce reactivity to stimuli and improve regulation, although these mechanisms have not been examined (using functional neuroimaging). Additionally, it is well-established that loneliness and inflammation are major risk factors for morbidity and mortality in older adults, although it is currently unknown whether mindfulness meditation training may reduce these risk factors. The purpose of the proposed study is to test if mindfulness meditation training (vs a wait-list control condition) reduces neurobehavioral reactivity and improves affect regulation in a sample of healthy older adults, as measured by functional magnetic resonance imaging. Additionally, we will examine whether mindfulness meditation training reduces loneliness and markers of inflammation.

Participants will be recruited in the Los Angeles area and randomly assigned to the 8-week Mindfulness-Based Stress Reduction (MBSR) intervention or to a wait-list. All participants will provide a blood sample and complete a psychosocial survey before and after the intervention, and complete a 60-minute neuroimaging assessment before and after the MBSR program. All participants who are randomly assigned to the wait-list will be offered the MBSR intervention after the 8-week intervention period and then complete an additional post-test assessment after completing the MBSR program (which will include a blood sample, psychosocial survey, and a neuroimaging assessment). Participants will complete neuroimaging tasks (where they will be presented with words, pictures, and sounds) before and after receiving the MBSR intervention, which will assess neural activity and regulation responses before and after mindfulness meditation training.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
The Effects of Mindfulness Meditation in Older Adults
Study Start Date :
Jan 1, 2008
Actual Primary Completion Date :
Jan 1, 2009
Actual Study Completion Date :
Jan 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mindfulness-Based Stress Reduction

A standardized 8-week mindfulness meditation training program

Behavioral: Mindfulness-Based Stress Reduction
8-week standardized mindfulness meditation training program
Other Names:
  • MBSR
  • No Intervention: Wait-List

    Outcome Measures

    Primary Outcome Measures

    1. Functional Neural Activity [Change from Baseline to 2 months]

      Neural responses to emotionally evocative stimuli

    Secondary Outcome Measures

    1. Pro-inflammation [Change from Baseline to 2 months]

      Genetic and protein measures of inflammation

    2. Loneliness [Change from Baseline to 2 months]

      self-reported loneliness

    3. Psychological Distress [Change from Baseline to 2 months]

      self-reported psychological distress

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    55 Years to 85 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • English-speaking adults between the ages of 55-85 years of age at time of entry

    • post-menopausal and not pregnant (women only)

    • Accessible geographically and willing to come to UCLA for all study related activities

    Exclusion Criteria:
    • they have regularly (>1 time per week) practiced a mind-body therapy anytime in the last six months (e.g., meditation, yoga, tai chi)

    • are not ambulatory, (c) indicate any treatment for mental health problems in the last six months

    • indicate any major physical health problems in the last three months

    • use medications affecting cardiovascular or endocrine function

    • are left-handed

    • or 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

    • smokers

    • indicate feeling claustrophobic in confined spaces, such as an fMRI scanner

    • weigh over 300 lbs

    • indicate any use of doctor prescribed cholesterol lowering medications (e.g., statins)

    • use any doctor prescribed pain medication

    • indicate any implants

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cousins Center for Psychoneuroimmunology, UCLA Los Angeles California United States 90095

    Sponsors and Collaborators

    • University of California, Los Angeles

    Investigators

    • Principal Investigator: J. David Creswell, Ph.D., University of California, Los Angeles

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    J. David Creswell, Post-Doctoral Fellow, Cousins Center for Psychoneuroimmunology, University of California, Los Angeles
    ClinicalTrials.gov Identifier:
    NCT01532596
    Other Study ID Numbers:
    • MBSR-Older-00001
    First Posted:
    Feb 14, 2012
    Last Update Posted:
    Feb 14, 2012
    Last Verified:
    Feb 1, 2012

    Study Results

    No Results Posted as of Feb 14, 2012