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Guided Meditation as an Adjunct to Enhance Postoperative Recovery

NCT03198039 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 29

Last updated 2024-06-04

No results posted yet for this study

Summary

The primary purpose of this trial is to test the feasibility of implementing a meditation program in the perioperative period.

Conditions

  • Feasibility of a Meditation Program Perioperatively

Interventions

BEHAVIORAL

Meditation

Isha Kriya (IK) meditation approximately 12 minutes, twice a day

Sponsors & Collaborators

Principal Investigators

  • Balachundhar Subramaniam, MD, MPH · Beth Israel Deaconess Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-28
Primary Completion
2020-04-30
Completion
2020-04-30

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03198039 on ClinicalTrials.gov