- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06673589
Brain-to-brain Synchrony in Ss With Different Levels of Social Interaction
November 13, 2024 updated by: Fred Travis, Maharishi International University
Brain-to-brain Synchrony as a Mechanism of Field Effects of Consciousness
Brain-to-brain synchrony will be measured between pairs of subjects with different levels of similarity of DNA and social interactions
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Brain-to-brain synchrony will be measured in five pairs of identical twins, five pairs who are good friends and from the same region of a country, and five pairs of strangers from different countries when they practice Transcendental Meditation practice
Study Type
Observational
Enrollment (Estimated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Frederick Travis, PhD
- Phone Number: 6414721209
- Email: ftravis@miu.edu
Study Contact Backup
- Name: Peter Hodak, PhD
- Phone Number: 6414721209
- Email: phodak@miu.edu
Study Locations
-
-
Iowa
-
Fairfield, Iowa, United States, 52556-3917
- Recruiting
- Maharishi International University
-
Contact:
- Peter Hodak, MA
- Phone Number: 6414721209
- Email: phodak@miu.edu
-
Principal Investigator:
- Frederick Travis, PhD
-
Contact:
- Frederick Travis, PhD
- Phone Number: 319-614-0357
- Email: ftravis@miu.edu
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
healthy adult population that practices TM
Description
Inclusion Criteria:
- healthy fit the cohort criteria practice TM
Exclusion Criteria:
- mental or physical issue
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Social Entanglement: Couples, good friends and strangeers
|
meditation practice
|
|
good friends from the same region of the country
Plus, extensive social interaction--daily
|
meditation practice
|
|
strangers from different countries
Interact minimally--less than once/week
|
meditation practice
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Brain-to-Brain Synchrony
Time Frame: 20 minute TM
|
EEG (electroencephalography) coherence between 32 sensors in the 10-10 System in all frequency bands
|
20 minute TM
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Tracing of depth of meditation (This is a graphic measure.)
Time Frame: after 20 minute meditation
|
Use a line to indicate depth of meditation
|
after 20 minute meditation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Fred Travis, PhD, Maharishi International Uniersity
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 (Actual)
November 1, 2024
Primary Completion (Estimated)
July 1, 2025
Study Completion (Estimated)
October 10, 2025
Study Registration Dates
First Submitted
June 17, 2024
First Submitted That Met QC Criteria
November 2, 2024
First Posted (Actual)
November 5, 2024
Study Record Updates
Last Update Posted (Actual)
November 15, 2024
Last Update Submitted That Met QC Criteria
November 13, 2024
Last Verified
November 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- MIU 001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
We are planning how to store 200 MB files in BDF format on a server
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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.
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