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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03779269
Other study ID # IRB-13-0045-CR03
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 14, 2017
Est. completion date December 14, 2025

Study information

Verified date September 2022
Source Orlando Regional Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this project is to assess impact of an 8 week course of Preksha Meditation (combination of Green color and buzzing sound meditation), in a group of college students to assess potential benefits to their pulmonary function, cognitive ability (immediate recall, attention), and happiness.


Description:

Preksha Meditation Research: The goal of this project is to assess impact of an 8 week course of Preksha Meditation (combination of Green color and buzzing sound meditation), in a group of college students to assess potential benefits to their pulmonary function, cognitive ability (immediate recall, attention), and happiness. The investigators will compare the data received from prior study to analyze their performance before and after. The investigators will also compare this data with control group data, to assess potential improvements as a benchmark. Analyse the EEG data to investigate its impact on brain. Further analyze their blood cells if they show any epigenetic changes. Data analysis team will be blinded for no identifiers are available. METHOD AND PROCEDURES: The data analysis will be undertaken by experts and will be blinded. The data currently is only de-identified. The data which is already collected from the research "Effect of Preksha Meditation (Green color and Buzzing Meditation) on Cognitive Abilities and Pulmonary Function in Students with a Control Group" will be analyzed. The data is related to students having practiced minimum 3 guided 25 minute sessions per week in a controlled environment. The control group did not meditate for those weeks when they enrolled in the program. The intervention the subjects received was as follows: Experimental group 3 days per week Sessions: 5 minutes: Relaxation and Review of Meditation Practices 10 minutes: Mahapraan Meditation 10 minutes: Green color meditation Begin in stages - 0 - 2 Weeks: Teach technique and carry out 15 minutes meditation sessions. - 2 - 9 Weeks: Increment meditation sessions to a length of 25 minutes. 5 minutes: Review of meditation experience and collection of information


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 142
Est. completion date December 14, 2025
Est. primary completion date February 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 24 Years
Eligibility Inclusion Criteria: - Healthy individuals - No prior experience in meditation Exclusion Criteria: - Prior experience with meditation. - health issues. - Alcohol - Smoking.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
meditation
meditation effect assessment using assessment tools.

Locations

Country Name City State
United States Florida International University Miami Beach Florida
United States Orlando Regional Medical Center Orlando Florida

Sponsors (2)

Lead Sponsor Collaborator
Orlando Regional Medical Center Florida International University

Country where clinical trial is conducted

United States, 

References & Publications (2)

Mehta S, Mehta V, Mehta S, Shah D, Motiwala A, Vardhan J, Mehta N, Mehta D. Multimodal behavior program for ADHD incorporating yoga and implemented by high school volunteers: a pilot study. ISRN Pediatr. 2011;2011:780745. doi: 10.5402/2011/780745. Epub 2011 Aug 11. — View Citation

Pragya SU, Cordoba G, Chiu R, Mehta N, Johnson P, Mehta DI, Mehta N. Can The Cognitive Parameters Of College Students With Learning Disabilities Benefit From Using Mahapraan, A Breathing Based Preksha Meditation. Journal of College Teaching & Learning 2014; 11, 4 Epub

Outcome

Type Measure Description Time frame Safety issue
Primary Cognitive skills assessment using Connor's CPT test Affect, short term memory, inattention, 8 weeks
Secondary Pulmonary function using actual lung capacity test Spirometry 8 weeks
Secondary Transcriptomics and epigenetics Upregulation and transcriptional profiling using fold change 8 weeks
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