FETZER: Use of a Functional Neuroimaging Battery for the Evaluation of a Meditation Retreat

Sponsor
Thomas Jefferson University (Other)
Overall Status
Completed
CT.gov ID
NCT02443766
Collaborator
(none)
14
1
61.9
0.2

Study Details

Study Description

Brief Summary

Over 2 decades scientists have been studying the effect on brain function from meditation practices. The purpose of this study is to measure the effect of a meditation retreat program on serotonin and dopamine transporter binding and changes in cerebral blood flow. The retreat program that will be followed is a week-long retreat called the Ignatian Retreat.

Condition or Disease Intervention/Treatment Phase
  • Other: Meditation Retreat

Detailed Description

This study will utilize DaTscan single photon emission computed tomography (SPECT) and functional magnetic resonance imaging (fMRI) in healthy subjects within one month of entering the retreat. The study uses DaTscan to measure the effect on serotonin and dopamine transporter binding, and functional magnetic resonance imaging (fMRI) to measure the effect on cerebral blood flow. The Ignatian Retreat is a weeklong retreat which involves meditation and prayer.

Additionally, study participants will complete a variety of questionnaires and scales to measure psychological and spirituality states. The scans and questionnaires will be completed before and after the participant has completed the retreat. The ultimate goal of the study is to analyze and compare pre and post imaging and neuropsychological and spirituality changes in healthy controls who participate in this retreat.

Study Design

Study Type:
Observational
Actual Enrollment :
14 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Use of a Functional Neuroimaging Battery for the Evaluation of a Meditation
Actual Study Start Date :
Jan 5, 2012
Actual Primary Completion Date :
Mar 2, 2017
Actual Study Completion Date :
Mar 2, 2017

Arms and Interventions

Arm Intervention/Treatment
Healthy Subjects

Healthy subjects will attend the weeklong meditation retreat.

Other: Meditation Retreat
Weeklong retreat which includes meditation and prayer.

Outcome Measures

Primary Outcome Measures

  1. Single Photon Emission Computed Tomography (SPECT) Imaging (DaTScan) [Within one month of the retreat]

    To detect changes in dopamine and serotonin before and after a meditation retreat program in serotonin transporter and dopamine transporter binding.

Secondary Outcome Measures

  1. functional MRI [Within one month of the retreat]

    To detect changes in cerebral blood flow before and after a meditation retreat program.

Other Outcome Measures

  1. Speilberger State Trait Anxiety Inventory (STAI) [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study. The Speilberger State Trait Anxiety Inventory (STAI) contains a total of 40 questions, half of which relate to the way subjects are feeling at the moment and half of which ask them to describe how they usually feel.

  2. Profile of Moods Scale (POMS) [Within one month of the retreat]

    The Profile of Mood States (POMS) is a validated questionnaire of 65 single word items that asks "How have you been feeling in the past week including today." The subjects will select their response to each word that describes a mood or feeling on a Likert scale from 1= Not at All, 2= A Little, 3=Moderately, 4=Quite a lot, to 5=Extremely. The responses are scored to generate values for Tension, Anger, Confusion, Depression and Vigor. The higher scores indicate a greater presence of that mood or state.

  3. Beck Depression Inventory (Beck 1972) [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study. The Beck Depression Inventory (Beck 1972) is a standard 21 item questionnaire probing cognitive and somatic symptoms of depression. The higher scores indicate a greater presence of depression.

  4. Standard Form-12 (SF-12) [Within one month of the retreat]

    This 12-item validated questionnaire will be used as one of the evaluation questionnaires for the study. The subjects will select their response to each word that describes a mood or feeling on a Likert scale.

  5. Hood Mysticism Scale (Lifetime) [Within one month of the retreat]

    This validated scale will be used as one of the evaluation questionnaires for the study. Items are rated on a five-point scale with negatively worded items reverse scored. The responses are scored to generate values for Extrovertive Mysticism, Religious Interpretation, and Introvertive Mysticism.

  6. Brief Multidimensional Measure of Religiousness/Spirituality [Within one month of the retreat]

    This 30-item validated questionnaire will be used as one of the evaluation questionnaires for the study. The responses are scored to generate values for Suffering, Positing Sharing, Crying, Emotional Attention, Feel for Others, and Emotional Contagion.

  7. Gratitude Questionnaire [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study. The subjects will select their response on a Likert scale. The higher scores indicate a greater sense of gratitude.

  8. Daily Spiritual Experience Scale [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study. This assessment measures ordinary, or daily, spiritual experiences.

  9. The Assessment of Spirituality and Religious Sentiments (ASPIRES ) [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study. This assessment measures Religious sentiments and Spiritual Transcendence.

  10. Index of Core Spiritual Experiences (INSPIRIT) [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study to evaluate the presence or frequency of certain religions.

  11. Functional Assessment of Chronic Illness Therapy Spiritual Well-Being (FACIT-Sp-12) [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study. The 12-item assessment is used to measure spiritual well-being by asking patients to describe aspects of spirituality and/or religious faith that contribute to health related quality of life.

  12. Cloninger Self-Transcendence Scale [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study. The subjects will select their response on a Likert scale. The higher scores indicate a greater presence to self-transcendence and well being.

  13. Five Facet Mindfulness Questionnaire [Within one month of the retreat]

    This validated questionnaire will be used as one of the evaluation questionnaires for the study.The analysis yielded five factors that appear to represent elements of mindfulness as it is currently conceptualized.The five facets are observing, describing, acting with awareness, non-judging of inner experience, and non-reactivity to inner experience.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Able to give informed consent and willing to complete the study.

  • Willing to undergo the full imaging procedures.

  • Women of childbearing potential with a negative serum pregnancy test.

Exclusion Criteria:
  • Any neurological or psychiatric disorders, including drug or alcohol abuse, that may interfere with cerebral blood flow as determined by the principal investigator.

  • Any medical conditions that may interfere with cerebral blood flow as determined by the principal investigator.

  • Currently taking medication that might affect cerebral blood flow (i.e. antidepressants, antipsychotics, anxiolytics, benzodiazepines, sedatives, antiseizure medications)

  • Subject is unable or unwilling to lie still in the scanner (i.e. due to claustrophobia or weight > 350 pounds)

  • Subject has metal in their body or other reason that they cannot undergo magnetic resonance imaging.

  • Previous brain surgery or intracranial abnormalities they may complicate interpretation of the brain scans. (e.g. stroke, tumor, vascular abnormality).

  • Pregnancy

  • Allergy to iodine or shellfish.

  • Concurrent participation in another research protocol that might affect the outcome of this study as determined by the principle Investigator.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Thomas Jefferson University Philadelphia Pennsylvania United States 19107

Sponsors and Collaborators

  • Thomas Jefferson University

Investigators

  • Principal Investigator: Andrew B. Newberg, MD, Thomas Jefferson University

Study Documents (Full-Text)

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Thomas Jefferson University
ClinicalTrials.gov Identifier:
NCT02443766
Other Study ID Numbers:
  • 11G.488
First Posted:
May 14, 2015
Last Update Posted:
Jul 25, 2022
Last Verified:
Jul 1, 2022

Study Results

No Results Posted as of Jul 25, 2022