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Perioperative Effect of Music in Patients Undergoing General Anesthesia (EMBAG)

Primary Purpose

Perioperative Anxiety, Postoperative Pain

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Music Therapy
Sponsored by
Dr. Negrin University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Perioperative Anxiety focused on measuring Anxiety, Perioperative, Insomnia

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients over 18 years of age and under 60 years of age
  • Classification of the American Society of Anesthesiologists (ASA) I-IV
  • Intervened on a scheduled basis for general surgery.
  • Signed informed consent prior to surgery.

Exclusion Criteria:

  • Refusal of the patient to participate in the study.
  • Patients under 18 years of age or incapable of giving their consent.
  • ASA V.
  • History of hypersensitivity to contact devices
  • Patients with total hearing impairment
  • Patients with substance abuse use disorders
  • Patients with cognitive deficit

Sites / Locations

  • Ángel BecerraRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control Group

Intervention Group

Arm Description

Patients randomized to the control group will be assessed for preoperative anxiety using the APAIS scale in the preoperative room and assessment of insomnia using the ISI scale both in the PACU and on the 1st day in the hospital ward. Pain assessment will be measured using the VAS scale in the PACU and on the first day on the hospital ward.

Patients randomized to the treatment with music group (classical music), after assessment of anxiety using the APAIS scale, will be given headphones and classical music will be played from their stay in the pre-surgery room, during surgery and in the PACU.

Outcomes

Primary Outcome Measures

Perioperative anxiety
Specific anxiety questionnaires (APAIS, STAI) will be applied on arrival at the pre-anesthesia room, prior to anesthetic induction and after arrival at the post-anesthetic recovery unit.

Secondary Outcome Measures

Postoperative pain
Postoperative pain will be assessed using the visual analog scale in the immediate postoperative period.

Full Information

First Posted
October 5, 2022
Last Updated
September 14, 2023
Sponsor
Dr. Negrin University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05572437
Brief Title
Perioperative Effect of Music in Patients Undergoing General Anesthesia
Acronym
EMBAG
Official Title
Perioperative Effect of Music in Patients Undergoing General Anesthesia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 15, 2022 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
October 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dr. Negrin University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Anxiety is a transient emotional state characterized by feelings of tension, apprehension, nervousness, fear, and heightened activation of the autonomic nervous system in response to a specific current or potential event or situation. Music therapy is a cost-effective and safe intervention applied to health care, that has been incorporated into different branches of medicine, including anesthesiology, showing economic benefits and as an adjunct to pharmacological therapy, allowing the use of lower doses of perioperative drugs, thus reducing their deleterious effects. The main objective of this randomized clinical trial is to evaluate whether the application of music during the perioperative period reduces perioperative anxiety in patients undergoing general and digestive surgery under general anesthesia.Patients between 18 and 60 years of age, classified according to the American Society of Anesthesiologists (ASA) I-IV, scheduled for general surgery and who have signed the informed consent, will be randomized to receive music therapy in the immediate perioperative period or not. Perioperative anxiety, stay in the PACU, incidence of postoperative pain and intraoperative opioid consumption will be compared between both groups.
Detailed Description
Anxiety is a transient emotional state characterized by feelings of tension, apprehension, nervousness, fear, and heightened activation of the autonomic nervous system in response to a specific current or potential event or situation. Music therapy is a cost-effective, non-invasive and safe intervention applied to health care, whose boom has grown gradually in recent years until it has been incorporated into different branches of medicine, including anesthesiology , showing economic benefits and as an adjunct to pharmacological therapy, since it allows the use of lower doses of some drugs, thus reducing their deleterious effects. The main objective of this randomized clinical trial is to evaluate whether the application of music during the perioperative period reduces perioperative anxiety in patients undergoing general and digestive surgery under general anesthesia. Patients between 18 and 60 years of age, classified according to the American Society of Anesthesiologists (ASA) I-IV, scheduled for general surgery and who have signed the informed consent, will be randomized to receive music therapy in the immediate perioperative period or not. Patients randomized to the control group will be assessed for preoperative anxiety using the APAIS and the STAI scales in the preoperative room and assessment of insomnia using the ISI scale both in the PACU and on the 1st day in the hospital ward. Pain assessment will be measured using the VAS scale in the PACU and on the first day in the hospital ward. Patients randomized to the treatment with music group (classical music), after assessment of anxiety using the APAIS and STAI scales, will be given headphones and classical music will be played from their stay in the pre-surgery room, during surgery and in the PACU.All patients will have their anxiety assessed in the pre-anesthesia room and insomnia assessed both in the PACU and on the 1st day in the hospital ward. Pain assessment will be measured in the PACU and on the first day in the hospitalization ward. Perioperative anxiety, stay in the PACU, incidence of postoperative pain and intraoperative opioid consumption will be compared between both groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Perioperative Anxiety, Postoperative Pain
Keywords
Anxiety, Perioperative, Insomnia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The randomization of the patients will be carried out by a collaborating researcher through a computer program (Excel 2016) at the time of inclusion in the study. This collaborating researcher will not be able to be present at the surgical intervention and will contact the nursing staff by telephone, indicating which patient should be given music therapy upon arrival in the pre-surgery room.
Masking
Care ProviderInvestigatorOutcomes Assessor
Masking Description
El investigador responsable de la recogida de los datos a partir del informe clínico de los anestesiólogos responsables del manejo clínico intra y postoperatorio de los pacientes no sabrá qué pacientes han sido incluidos en el grupo Intervención.
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Patients randomized to the control group will be assessed for preoperative anxiety using the APAIS scale in the preoperative room and assessment of insomnia using the ISI scale both in the PACU and on the 1st day in the hospital ward. Pain assessment will be measured using the VAS scale in the PACU and on the first day on the hospital ward.
Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
Patients randomized to the treatment with music group (classical music), after assessment of anxiety using the APAIS scale, will be given headphones and classical music will be played from their stay in the pre-surgery room, during surgery and in the PACU.
Intervention Type
Device
Intervention Name(s)
Music Therapy
Intervention Description
Patients randomized to the treatment with music group (classical music), after assessment of anxiety using the APAIS scale, will be given headphones and classical music will be played from their stay in the pre-anesthesia room, during surgery and in the PACU.
Primary Outcome Measure Information:
Title
Perioperative anxiety
Description
Specific anxiety questionnaires (APAIS, STAI) will be applied on arrival at the pre-anesthesia room, prior to anesthetic induction and after arrival at the post-anesthetic recovery unit.
Time Frame
from the arrival to the preanesthesia room to the 4 postoperative hour
Secondary Outcome Measure Information:
Title
Postoperative pain
Description
Postoperative pain will be assessed using the visual analog scale in the immediate postoperative period.
Time Frame
From the first postoperative hour to the 4th postoperative hour.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients over 18 years of age and under 60 years of age Classification of the American Society of Anesthesiologists (ASA) I-IV Intervened on a scheduled basis for general surgery. Signed informed consent prior to surgery. Exclusion Criteria: Refusal of the patient to participate in the study. Patients under 18 years of age or incapable of giving their consent. ASA V. History of hypersensitivity to contact devices Patients with total hearing impairment Patients with substance abuse use disorders Patients with cognitive deficit
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ángel Becerra, PhD
Phone
+34676229025
Email
angbecbol@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ángel Becerra, PhD
Organizational Affiliation
Hospital Universitario de Gran Canaria Doctor Negrín
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ángel Becerra
City
Las Palmas De Gran Canaria
State/Province
Las Palmas
ZIP/Postal Code
35019
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ángel Becerra, MD
Phone
+34676229025
Email
angbecbol@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD are to be shared with other researchers when required once the study is completed and global data are published.

Learn more about this trial

Perioperative Effect of Music in Patients Undergoing General Anesthesia

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