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Clinical Trials/NCT01975415
NCT01975415CompletedNot Applicable

Digital Medicine in Meditation

Scripps Translational Science Institute1 site in 1 country40 target enrollmentStarted: October 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
Blood Pressure

Study Overview

Brief Summary

This study will investigate the acute response to meditation during a week-long meditation retreat at the Chopra Center as measured by the continuous, simultaneous monitoring of numerous biometric parameters in selected cohorts of experienced and novice meditators during periods of meditation and specific breathing techniques. Comparisons between cohorts as well as over time will allow for the identification of meditation and/or breathing-related changes.

Detailed Description

The biometric responses to meditation and breathing techniques will be compared between novice and experienced meditators, as well as initial versus final biometric responses in all participants stratified by cohort. Investigators hypothesize that novice meditators will experience a measurable change in response to mediation over the week-long retreat, whereas experienced meditators will demonstrate a more robust response than novice meditators on the first day of the retreat with less change over the retreat.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adult over age 18 who are already registered to participate in the week-long "Seduction of the Soul" retreat.
  • Capable of providing informed consent

Exclusion Criteria

  • Chronic requirement for daily use of chronotropically active medications including beta-blockers, non-dihydropyridine calcium channel blockers, clonidine or beta-agonist inhalers.
  • Implantable pacemaker or cardioverter-defibrillator.
  • Known allergy to adhesives.

Outcomes

Primary Outcomes

Blood Pressure

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

Non-invasive blood pressure

ECG

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

5-lead electrocardiogram

Respiration rate

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

Respiration rate

Heart Rate

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

Heart rate

Oxygen saturation (SpO2)

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

Oxygen saturation

Skin temperature

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

Skin temperature

Heart rate variability

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

Variability in heart rate across a period of time.

EEG

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

14-lead Electroencephalogram

Stress level

Time Frame: Participants will be measured at Day 1 and Day 5 of retreat

Stress level calculated from heart rate variability

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Scripps Translational Science Institute
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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