Transfer of Neural Energy Between Humans

Transfer of Neural Energy Between Human Subjects

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.

Study Overview

Status

Completed

Conditions

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 Type

Observational

Enrollment

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Washington
      • Kenmore, Washington, United States, 98028
        • Bastyr University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2000

Study Completion

January 1, 2004

Study Registration Dates

First Submitted

January 29, 2002

First Submitted That Met QC Criteria

January 29, 2002

First Posted (Estimate)

January 30, 2002

Study Record Updates

Last Update Posted (Estimate)

August 18, 2006

Last Update Submitted That Met QC Criteria

August 17, 2006

Last Verified

July 1, 2006

More Information

Terms related to this study

Other Study ID Numbers

  • R21AT000287-01 (U.S. NIH Grant/Contract)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Healthy

3
Subscribe