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Clinical Trials/NCT04551469
NCT04551469
Active, not recruiting
Not Applicable

A Randomized Clinical Trial to Measure Efficacy of Music on Cardiac Surgery

Massachusetts General Hospital1 site in 1 country120 target enrollmentJuly 1, 2021
ConditionsCardiac Surgery

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Surgery
Sponsor
Massachusetts General Hospital
Enrollment
120
Locations
1
Primary Endpoint
Change in Serum Cortisol
Status
Active, not recruiting
Last Updated
7 months ago

Overview

Brief Summary

Cardiac surgery involves both physical and psychological stress for patients from time of decision to the recovery period. The physical aspects and the impact on the psychological experience makes the post-operative period a difficult time for patients. Patients often experience emotional distress, uncertainty, and fear. A non-pharmacological intervention of music may affect the patient's perception of early recovery with little to no side effects.

Current research has demonstrated efficacy in psychological and physical responses. there is limited data on the endocrinologic (cortisol) and immunologic biomarkers Immunoglobulin A to a music intervention. Therefore, the purpose of this study is to measure both psychological/physical response and biomarkers pre and post a 30-minute music intervention compared to standard of care experience A randomized, placebo-controlled, pre-post clinical trial will be initiated to demonstrate the effect that music has on the primary outcome of serum cortisol and secondary outcomes of anxiety, pain, blood pressure, heart rate, respirations, and Immunoglobulin A in adult patients after cardiac surgery.

Detailed Description

One hundred-twelve subjects will be enrolled, 56 subjects in the treatment and 56 subjects in the standard of care group. It was estimated this sample size would be needed to detect a medium effects size of .30 with an alpha set at a level of .05. Patients, who agree to participate, will be randomly allocated to one of two groups, treatment and standard of care group using a computer-generated randomization scheme. On post-operative day one, two or three, a 30-minute music period will be used through personal headphones and a MP3 device. Music will be a selection that is symphonic music that has no dramatic changes. The standard of care group will listen to environmental sounds in the Cardiac Surgical Intensive Care Unit. Psychological, and physical responses as well as biomarkers will be collected pre and then 30 minutes after the start of the intervention period in both groups. The psychological response will be assessed by the Spielberger State Anxiety Scale to measure state anxiety and a visual analogue scale for measurement of pain. Physical responses will be collected that includes Blood pressure in mmHg, heart rate in beats per minute and respirations in beats per minute. The biomarkers collected will be serum cortisol measured in micrograms per deciliter and Immunoglobulin in milligrams per deciliter. Descriptive statistics will be used to describe the sample and the outcomes measure will be compared using a student t-test.

Registry
clinicaltrials.gov
Start Date
July 1, 2021
End Date
December 30, 2025
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Diane L. Carroll

nurse researcher

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients in the Cardiac Surgical Intensive Care Unit or the Cardiac Surgical Step Down Unit after undergoing heart valve replacement/repair and/or coronary artery bypass surgery, or aortic repair over the age of 18 years, hemodynamically stable, extubated and able to hear music.

Exclusion Criteria

  • Patients that are deaf, hemodynamically unstable, intubated, and on infectious disease precautions after surgery.

Outcomes

Primary Outcomes

Change in Serum Cortisol

Time Frame: Change in serum cortisol before and 30 minutes after start of intervention period

micrograms per deciliter

Secondary Outcomes

  • Perceived Pain Level(Change in pain level before and 30 minutes after start of intervention period)
  • Anxiety(Change in state anxiety before and 30 minutes after start of intervention period)
  • Blood Pressure(Change in blood pressure before and 30 minutes after start of intervention period)
  • Heart Rate(Change in heart rate before and 30 minutes after start of intervention period)
  • Respirations(Change in respirations before and 30 minutes after start of intervention period)
  • Serum Immunoglobulin A(Change in serum immunoglobulin A before and 30 minutes after start of intervention period)

Study Sites (1)

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