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

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

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04551469
Enrollment
120
Registered
2020-09-16
Start date
2021-07-01
Completion date
2025-12-30
Last updated
2025-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgery

Keywords

music, cardiac surgery, anxiety

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.

Interventions

BEHAVIORALmusic

Music intervention for 30 minutes

Sponsors

Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Serum CortisolChange in serum cortisol before and 30 minutes after start of intervention periodmicrograms per deciliter

Secondary

MeasureTime frameDescription
AnxietyChange in state anxiety before and 30 minutes after start of intervention periodSpielberger State Anxiety Scale (STAI) -2 0 to 80 with higher score more Anxiety.
Perceived Pain LevelChange in pain level before and 30 minutes after start of intervention periodVisual Analogue Pain Scale- 0 to 10 with 0 = no pain to 10=worst pain.
Blood PressureChange in blood pressure before and 30 minutes after start of intervention periodmm Hg
Heart RateChange in heart rate before and 30 minutes after start of intervention periodbeats per minute
RespirationsChange in respirations before and 30 minutes after start of intervention periodbreaths per minute
Serum Immunoglobulin AChange in serum immunoglobulin A before and 30 minutes after start of intervention periodmg per deciliter

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026