跳至主要内容
临床试验/NCT04551469
NCT04551469进行中(未招募)不适用

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

Massachusetts General Hospital2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2021年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
120
试验地点
2
主要终点
Change in Serum Cortisol

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

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

结局指标

主要结局

Change in Serum Cortisol

时间窗: Change in serum cortisol before and 30 minutes after start of intervention period

micrograms per deciliter

次要结局

  • 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)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Diane L. Carroll

nurse researcher

Massachusetts General Hospital

研究点 (2)

Loading locations...

相似试验