Actively Recruiting
The Effect of Music on Anxiety and Vasospasm in Patients Undergoing Transradial Angiography
Led by Mersin University · Updated on 2025-01-31
90
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Cardiovascular diseases are a major health concern worldwide, leading to high rates of death and illness. In Turkey, circulatory and ischemic heart diseases are responsible for a large percentage of deaths, with coronary artery disease (CAD) being the most common. Coronary angiography is considered the best invasive method to diagnose CAD, but the procedure can cause anxiety and fear due to its invasive nature and unfamiliar environment. Anxiety may also contribute to radial artery spasms during the procedure, which is a concern because the radial artery is prone to spasms due to its structure. This study is a randomized controlled trial conducted in a hospital's Coronary Angiography Unit to evaluate the effect of music on anxiety and radial artery spasms during transradial coronary angiography. Ninety patients will be randomly assigned to either an intervention group, which will listen to Classical Turkish Music via headphones during the procedure, or a control group receiving standard care without music. Both groups will undergo the same coronary angiography procedure performed by the same physician using the same equipment. Participants will complete anxiety assessments before and after the procedure using the State Anxiety Inventory. Radial artery spasms will be monitored and recorded based on specific symptoms during the angiography. Patients will be observed for bleeding and recovery times post-procedure, with discharge timing depending on whether additional interventions are performed. Data collection will continue from October 2024 to April 2025, and safety will be monitored throughout the study.
CONDITIONS
Brief Title
The Effect of Music on Anxiety and Vasospasm in Patients Undergoing Transradial Angiography
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Indication for radial coronary angiography due to non-acute coronary syndrome reasons
- Undergoing coronary angiography for the first time
- Aged 18 years or older
- Conscious, oriented, and cooperative
- Able to read and understand Turkish
- Willing to participate in the study
- Without any physical limitations preventing music listening
- Without a diagnosis of hearing loss
- Not using a hearing aid
- Without a diagnosis of anxiety disorder
- Without any mental health disorders
- Having signed the "Voluntary Informed Consent Form.
You will not qualify if you...
- Indication for radial coronary angiography due to acute coronary syndrome
- Previous history of coronary angiography
- Under the age of 18
- Unconscious, disoriented, or uncooperative
- Unable to read or understand Turkish
- Unwilling to participate in the study
- Having physical limitations that prevent listening to music
- Diagnosed with hearing loss
- Using a hearing aid
- Diagnosed with an anxiety disorder or taking medication for anxiety
- Having a mental health disorder
- Not signing the "Voluntary Informed Consent Form."
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Duration - Day of procedure
Participants undergo transradial coronary angiography. Those in the intervention group listen to classical Turkish music through headphones during the procedure, while those in the control group receive standard care without music.
1 visit (in-person)
Duration - 6 hours to 1 day
Participants are monitored after the angiography procedure. Those without percutaneous coronary intervention are observed for 6 hours before discharge. Participants who undergo percutaneous coronary intervention are monitored in the cardiology clinic for one day post-procedure.
Approximately 1 post-procedure observation period
Trial Site Locations
Total: 1 location
1
Mersin Universiy Faculty of Nursing
Mersin, yenisehir, Turkey (Türkiye), 33343
Actively Recruiting
Research Team
N
Nida YESIL, Graduate Nursing Student
E
Emrah YESİL, specialist doctor
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
2
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