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Effect of music therapy on comfort of patients undergoing open heart surgery

Effect of music therapy on comfort of open heart surgery patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201310234443N6
Enrollment
62
Registered
2013-12-04
Start date
2013-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Heart surgery. Other functional disturbances following cardiac surgery

Interventions

Intervention 1: Intervention: Playing instrumental and relaxing music through headphones for half an hour. Intervention 2: Control: Resting on bed for half an hour.
Intervention: Playing instrumental and relaxing music through headphones for half an hour.
Control: Resting on bed for half an hour.

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Willingness to participate in the study; Undergoing non-emergency open heart surgery for the first time; Age between 30 to 75 years old; Stabile hemodynamic condition such as systolic blood pressure higher than 90 mmHg, lack of life threatening dysrhythmia and a heart rate between 60 and 100 bpm; Having no mental disorders; Understanding Persian language; Not drug and alcohol addicted; Willingness to hear music; Having no hearing impairment that prevents using headphones; Being conscious and oriented to time, place and person; Undertaking a routine surgical procedure in the operating room such as saphenous vein graft without unexpected events such as severe bleeding or prolong operation; Having no underlying chronic disease that disturb patient comfort such as discopathy. Exclusion criteria: Suffering from acute complications associated with surgery such as bleeding more than 200cc/h of chest tubes, cardiac tamponade, life threatening dysrhythmias or any emergency condition that requires immediate intervention; Willingness to quit from the study; Death during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Comfort. Timepoint: Immediately before and after the clinical trial. Method of measurement: kolcaba General Comfort Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElyas Soltani

Tehran University of Medical Sciences

soltani_75@yahoo.comsoltani.chenar@gmail.com+98 21 6694 3187

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026