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Inattention and MemoryNCT03779269

Effect of Preksha Meditation on Cognitive Abilities and Pulmonary Function in Students

A study testing meditation in people with Inattention and Memory and Affect, run by Orlando Regional Medical Center at 2 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 18 to 24 yearsHealthy volunteers can take part
Conditions the study is for
Inattention and Memory, Affect
What is being tested?
meditation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
142 participants
Where
2 sitesUnited States
Study dates
14 May 2017to 10 Oct 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 24 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Healthy individuals
  • No prior experience in meditation

Who cannot join

  • Prior experience with meditation.
  • health issues.
  • Alcohol
  • Smoking.

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Florida International University

    Miami Beach, Florida, 33199

  • Orlando Regional Medical Center

    Orlando, Florida, 32806

Other trials in United States

About this study

Official title: Effect of Preksha Meditation (Green Color and Buzzing Meditation) on Cognitive Abilities and Pulmonary Function in Students With a Control Group

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.

Read the detailed 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
Being tested
meditation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • meditationOther

    meditation effect assessment using assessment tools.

Study groups in NCT03779269
Study groupRoleWhat they receive
color meditationExperimentalonly color meditation
Receives: Other: meditation
Sound meditationExperimentalOnly sound mediation
Receives: Other: meditation
Color and sound combined meditationExperimentalCombined group
Receives: Other: meditation
Control groupNo interventionOnly control group

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Cognitive skills assessment using Connor's CPT test

    Affect, short term memory, inattention,

    Measured: 8 weeks

Secondary outcomes (2)
  1. Pulmonary function using actual lung capacity test

    Spirometry

    Measured: 8 weeks

  2. Transcriptomics and epigenetics

    Upregulation and transcriptional profiling using fold change

    Measured: 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Dec 2018
  2. Study start14 May 2017
  3. Primary completion1 Feb 2022
  4. Study completion10 Oct 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Non-randomised
Intervention model
Single group
Model description
prospective convenience controlled study
Masking
None (open label)
Enrolment
142 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03779269
Sponsor's protocol ID
IRB-13-0045-CR03
Status last verified
Oct 2026
First submitted
6 Dec 2018
Last updated
15 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: De-identified summary data

Publications

  • 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.

    PubMed 22389788
  • 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

  • Abomoelak B, Kapoor N, Schreck M, Pragya SU, Pragya SC, Mehta N, Bozelli JC Jr, Shanmuganathan M, Kroezen Z, Britz-Mckibbin P, Uddin P, Veeramachaneni P, Mehta N, Prather R, Mehta A, Mehta D. Preksha Dhyana meditation modulates the serum metabolome in healthy and meditation-naive participants. Front Mol Biosci. 2026 Apr 15;13:1741802. doi: 10.3389/fmolb.2026.1741802. eCollection 2026.

    PubMed 42064595
  • Pragya SU, Pragya SC, Griswold AJ, Gu E, Mehta ND, Uddin P, Veeramachaneni P, Mehta N, Mehta D, Abomoelak B. Preksha Dhyana Meditation Effect on the DNA Methylation Signature in College Students. J Integr Complement Med. 2023 Apr;29(4):224-233. doi: 10.1089/jicm.2022.0713. Epub 2023 Feb 7.

    PubMed 36749149
  • Pragya SU, Mehta ND, Abomoelak B, Uddin P, Veeramachaneni P, Mehta N, Moore S, Jean-Francois M, Garcia S, Pragya SC, Mehta DI. Effects of Combining Meditation Techniques on Short-Term Memory, Attention, and Affect in Healthy College Students. Front Psychol. 2021 Mar 5;12:607573. doi: 10.3389/fpsyg.2021.607573. eCollection 2021.

    PubMed 33746830

Questions about this trial

What is this clinical trial studying?

A study testing meditation in people with Inattention and Memory and Affect, run by Orlando Regional Medical Center at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Cognitive skills assessment using Connor's CPT test (time frame: 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03779269, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Oct 2026.

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