Clinical Trials Directory

Trials / Completed

CompletedNCT03198039

Guided Meditation as an Adjunct to Enhance Postoperative Recovery

Guided Meditation as an Adjunct to Enhance Postoperative Recovery: A Feasibility Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
29 (actual)
Sponsor
Beth Israel Deaconess Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

This is a prospective, randomized, controlled study involving 30 adult patients undergoing cardiac surgery. Investigators will test the feasibility of implementing a meditation program in the perioperative period. Patients will be randomized to one of three groups: those who complete Isha Kriya (IK) meditation before and after surgery, those who complete postoperative IK meditation only, and those who receive the standard of care with no meditation intervention. In addition to testing feasibility, the investigators will explore whether a meditation program can affect recovery after surgery. Patients enrolled will be followed postoperatively for up to one month to assess their cognitive function, pain, and sleep. Blood will also be collected for analysis of biomarkers of inflammation.

Conditions

Interventions

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

Timeline

Start date
2017-11-28
Primary completion
2020-04-30
Completion
2020-04-30
First posted
2017-06-23
Last updated
2024-06-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03198039. Inclusion in this directory is not an endorsement.