NCT07322562

Brief Summary

Music therapy has been reported to reduce analgesic and anesthetic requirements, but evidence in thoracic surgery remains limited. This prospective observational study aimed to evaluate the effects of different music types on hemodynamic stability and anesthetic consumption in patients undergoing thoracic surgery.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
159

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Oct 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

December 15, 2025

Completed
16 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

January 7, 2026

Completed
Last Updated

February 17, 2026

Status Verified

October 1, 2025

Enrollment Period

3 months

First QC Date

December 15, 2025

Last Update Submit

February 16, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • anesthetic consumption

    desfluran consumption during surgery (mL)

    during surgery

  • anesthetic consumption

    Induction propofol dose (mg)

    during induction of anesthesia

Secondary Outcomes (4)

  • hemodynamic parameters

    during surgery, 48 hour after surgery

  • hemodynamic parameters

    during surgery, 48 hour after surgery

  • hemodynamic parameters

    during surgery, 48 hour after surgery

  • hemodynamic parameters

    during surgery, 48 hour after surgery

Study Arms (3)

Group 1: Sufi music group

In the sufi music group, sufi music was played through over-ear headphones; the volume was adjusted based on patient comfort and confirmed with the patient. Music playback was initiated alongside routine monitoring and continued throughout the surgery, ending when the patient was transferred to the stretcher after extubation.

Other: music therapy during surgery

Group 2: Classical Western music group

In the classical Western music group, music was played through over-ear headphones; the volume was adjusted based on patient comfort and confirmed with the patient. Music playback was initiated alongside routine monitoring and continued throughout the surgery, ending when the patient was transferred to the stretcher after extubation.

Other: music therapy during surgery

Group 3: no music group

In the no music group, the patient was not allowed to listen to any type of music during surgery.

Interventions

In the music groups, music was played through over-ear headphones; the volume was adjusted based on patient comfort and confirmed with the patient. Music playback was initiated alongside routine monitoring and continued throughout the surgery, ending when the patient was transferred to the stretcher after extubation. For infection control purposes, headphone sponges were changed for each patient.

Group 1: Sufi music groupGroup 2: Classical Western music group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

All patients who will undergo thoracic surgery under general anesthesia and meet the criteria of being over 18 years of age

You may qualify if:

  • Age 18 and over,
  • American Society of Anesthesiologists (ASA) classification I-III,
  • No hearing acuity,
  • Volunteer to participate in the study,
  • Cooperative and oriented,
  • No history of psychiatric illness and/or psychiatric medication use,

You may not qualify if:

  • Patients who were under 18 years,
  • ASA classification \>III,
  • had hearing loss,
  • had a psychiatric diagnosis and/or were taking antipsychotic/antidepressant/mood stabilizer medications,
  • were uncooperative (dementia, mental retardation, etc.),
  • Major complications during the intraoperative or postoperative period, (respiratory failure, hemodynamic instability, hypoxia, serious arrhythmia, cardiac arrest, etc.)
  • Emergency surgery,
  • had a history of alcohol or drug abuse,
  • did not speak Turkish,
  • did not consent to participate in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cukurova University Faculty of Medicine Anesthesiology Department

Adana, Adana, 01380, Turkey (Türkiye)

Location

Study Officials

  • Mediha Turktan, M.D.

    Cukurova University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principal investigator

Study Record Dates

First Submitted

December 15, 2025

First Posted

January 7, 2026

Study Start

October 1, 2025

Primary Completion

December 31, 2025

Study Completion

December 31, 2025

Last Updated

February 17, 2026

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations