Mindfulness Meditation in Older Adults

Early Phase 1

Completed

• Conditions: Aging
• Interventions: Behavioral: Mindfulness-Based Stress Reduction

• Registration Number: NCT01532596
• Lead Sponsor: University of California, Los Angeles

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.

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.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2008-01
• Primary Completion: 2009-01
• Study Completion: 2009-01
• Status Verified: 2012-02
• Study First Submitted: 2012-02-08
• Study First Submitted QC: 2012-02-09
• Last Update Submitted: 2012-02-09
• Study First Posted: 2012-02-14
• Last Update Posted: 2012-02-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

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

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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

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Mindfulness-Based Stress Reduction	Mindfulness-Based Stress Reduction	A standardized 8-week mindfulness meditation training program

Primary Outcome Measures

Name	Time	Method
Functional Neural Activity	Change from Baseline to 2 months	Neural responses to emotionally evocative stimuli

Secondary Outcome Measures

Name	Time	Method
Pro-inflammation	Change from Baseline to 2 months	Genetic and protein measures of inflammation
Loneliness	Change from Baseline to 2 months	self-reported loneliness
Psychological Distress	Change from Baseline to 2 months	self-reported psychological distress

Trial Locations

Locations (1)

Cousins Center for Psychoneuroimmunology, UCLA; 🇺🇸 Los Angeles, California, United States