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OpenTrials
Completed

NCT Number: NCT01532596

Mindfulness Meditation in Older Adults

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.

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Key information

Conditions

Age range

55 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Cousins Center for Psychoneuroimmunology, UCLA

Los Angeles, California, 90095, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Mindfulness-Based Stress Reduction

Behavioral

8-week standardized mindfulness meditation training program

Other names: MBSR

Primary outcomes

  1. Functional Neural Activity

    Time frame: Change from Baseline to 2 months

    Neural responses to emotionally evocative stimuli

Secondary outcomes

  1. Pro-inflammation

    Time frame: Change from Baseline to 2 months

    Genetic and protein measures of inflammation

  2. Loneliness

    Time frame: Change from Baseline to 2 months

    self-reported loneliness

  3. Psychological Distress

    Time frame: Change from Baseline to 2 months

    self-reported psychological distress

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Registry information

Official study title

The Effects of Mindfulness Meditation in Older Adults

Acronym: MIND

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Feb 14, 2012
Registry last updated
Feb 14, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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