Key result
Trial protocol evaluates guided meditation to enhance postoperative recovery after cardiac surgery.
Why the study?
Postoperative neurological complications and perioperative depression and anxiety after cardiac surgery impair recovery and quality of life, and mind-body prehabilitation interventions may improve outcomes.
Does Isha Kriya guided meditation improve postoperative recovery and is it feasible to implement in adult patients undergoing cardiac surgery?
RCT (n=40)
Assessor blinded
Block randomization in a 1:1:1 allocation
No
Does Isha Kriya guided meditation improve postoperative recovery and is it feasible to implement in adult patients undergoing cardiac surgery?
This study protocol describes a randomized feasibility trial to evaluate the implementation and potential benefits of a perioperative guided meditation program for patients undergoing cardiac surgery.
BACKGROUND: Cardiac surgical procedures are associated with postoperative neurological complications such as cognitive decline and delirium, which can complicate recovery and impair quality of life. Perioperative depression and anxiety may be associated with increased mortality after cardiac surgeries. Surgical prehabilitation is an emerging concept that includes preoperative interventions to potentially reduce postoperative complications. While most current prehabilitation interventions focus on optimizing physical health, mind-body interventions are an area of growing interest. Preoperative mind-body interventions such as Isha Kriya meditation, may hold significant potential to improve postsurgical outcomes. METHODS: This is a prospective, randomized controlled feasibility trial. A total of 40 adult patients undergoing cardiac surgery will be randomized to one of three study groups. Participants randomized to either of the two intervention groups will receive meditative intervention: (1) commencing two weeks before surgery; or (2) commencing only from the day after surgery. Meditative intervention will last for four weeks after the surgery in these groups. Participants in the third control group will receive the current standard of care with no meditative intervention. All participants will undergo assessments using neurocognitive, sleep, depression, anxiety, and pain questionnaires at various time points in the perioperative period. Blood samples will be collected at baseline, preoperatively, and postoperatively to assess for inflammatory biomarkers. The primary aim of this trial is to assess the feasibility of implementing a perioperative meditative intervention program. Other objectives include studying the effect of meditation on postoperative pain, sleep, psychological wellbeing, cognitive function, and delirium. These will be used to calculate effect size to design future studies. DISCUSSION: This study serves as the first step towards understanding the feasibility of implementing a mind-body intervention as a prehabilitative intervention to improve postoperative surgical outcomes after cardiac surgery. TRIAL REGISTRATION: Clinicaltrials.gov, NCT03198039 . Registered on 23 June 2017.
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Packiasabapathy et al. (2019) conducted an RCT in Cardiac surgery (n=40). Isha Kriya guided meditation vs. Standard of care was evaluated on Feasibility of implementing a meditation routine in the perioperative period (adherence). This paper is a study protocol for a randomized controlled feasibility trial evaluating guided meditation to enhance postoperative recovery after cardiac surgery, and contains no clinical results.
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