Transfer of Neural Energy Between Humans

Sponsor
National Center for Complementary and Integrative Health (NCCIH) (NIH)
Overall Status
Completed
CT.gov ID
NCT00029978
Collaborator
(none)
60
1
40
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Study Details

Study Description

Brief Summary

The purpose of this study is to determine whether visual evoked potentials generated in one human brain by photostimulation can generate a correlated EEG signal in the brain of another human subject who is located at a distance and who is not visually stimulated.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study will attempt to replicate findings suggesting that visual evoked potentials generated in one human brain (Subject A) by photostimulation can generate a correlated EEG signal in the brain of another human subject (subject B) who is located at a distance (14.5 meters) and who is not visually stimulated.

    This project will occur in three stages. First we will identify pairs of subjects who have cross-correlated evoked potentials during photostimulation to Subject A at the p < .01 level of significance. If no pairs can be identified we will continue to enroll and test up to 50 pairs of subjects. If pairs of subjects that demonstrate the phenomenon cannot be identified using this p value by the end of the project time line we will reject the hypothesis that remote transfer of neural energy occurs and report failure to replicate the original study. If we detect greater than or equal to 5 pairs of subjects who meet the criteria we will attempt to replicate in those pairs using a higher criteria of p < .001. If Grinberg-Zylberbaum et al's experiment can be replicated at both stages, the project team will go to stage 3 to investigate the same phenomenon in the identified pairs of human subjects using functional magnetic resonance imaging (fMRI) as a second independent neurophysiological measure of transfer of information between two human brains. We will record fMRIs (occipital, temporal, frontal and parietal) in the remote individual while their counterpart, located in a separate chamber, is receiving light stimulation in an on-off pattern. We will determine if there are statistically significant differences in digitized fMRI during lights on vs. lights off conditions. The main outcome measures for this project will be the binary (yes-no) output from statistical analysis using cross-correlational and z-score testing for the detection of a transferred evoked signal (in both EEG and fMRI experiments) in Subject B. Appropriate controls will be used. If replicated, this study will provide a useful technology and method to quantitatively investigate the characteristics and neural mechanisms of remote effects of "mental events." Such experimental methods will assist in the investigation of basic mechanisms involved in "mind-body" medicine.

    Study Design

    Study Type:
    Observational
    Observational Model:
    Defined Population
    Time Perspective:
    Cross-Sectional
    Official Title:
    Transfer of Neural Energy Between Human Subjects
    Study Start Date :
    Sep 1, 2000
    Study Completion Date :
    Jan 1, 2004

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 65 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      • Pairs of healthy human volunteers 18-65 years of age who know each other and who each answered "yes" to the following statement: "I have had at least one experience of feeling the presence of a friend/relative/partner even when we are not physically together."

      • Subjects have at least one year experience practicing meditation, relaxation techniques, contemplation or prayer at least once a week.

      • Willingness to report to the University of Washington on at least 1-2 occasions and up to a maximum of 6 visits, for 1-2 hour sessions each visit.

      • Willingness to undergo FreezeFrame relaxation training in a 8 minute session.

      • Willingness to have EEG and EKG measurements.

      • Willingness to undergo functional MRI evaluation for 45-60 minutes in a small horizontal chamber and to be exposed to high decibel auditory stimulation during the procedure (optional).

      • Ability to provide informed consent.

      • Visual acuity 20/20 or better in each eye, with correction.

      Exclusion Criteria

      • Diagnosis of neurological disease, including epilepsy. History of epilepsy.

      • Diagnosis of psychiatric disorder either past or current.

      • Visual acuity more than 25/25 in each eye, with correction.

      • Implanted devices or metal objects such as pacemakers, aneurysm clips, metal bone or joint pins, or shrapnel (in case of willingness to participate in fMRI part of the study).

      • Current use of psychotropic medications, either prescription or illicit.

      • History of self-reported claustrophobia (in case of willingness to participate in fMRI part of the study).

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Bastyr University Kenmore Washington United States 98028

      Sponsors and Collaborators

      • National Center for Complementary and Integrative Health (NCCIH)

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Additional Information:

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00029978
      Other Study ID Numbers:
      • R21AT000287-01
      First Posted:
      Jan 30, 2002
      Last Update Posted:
      Aug 18, 2006
      Last Verified:
      Jul 1, 2006

      Study Results

      No Results Posted as of Aug 18, 2006