Actively Recruiting
The Effect of Quranic Recitation and Classical Music on Postoperative Pain Intensity and Interleukin-6 Levels in Lower Limb Orthopedic Surgery With Intrathecal Anesthesia
Led by Universitas Jenderal Soedirman · Updated on 2024-12-03
33
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effects of murottal (recitations of Islamic verses) and classical music on reducing postoperative pain intensity and levels of interleukin 6, an inflammatory marker, in patients undergoing lower extremity orthopedic surgery with spinal anesthesia. The study aims to understand if these non-drug therapies can help manage pain and the body's inflammatory response after surgery. Participants are randomly assigned to one of three groups: listening to murottal during surgery recovery, listening to classical music, or receiving standard postoperative care without additional interventions. Pain intensity and interleukin 6 levels will be measured before surgery and 30 minutes after surgery to assess the impact of the interventions. Throughout the study, participants will undergo routine checkups to ensure safety and treatment success. Pain will be measured using a numeric rating scale, and blood samples will be collected to track interleukin 6 levels. The study will monitor participants closely during the postoperative period to evaluate the effects of these therapies compared to standard care.
CONDITIONS
Brief Title
Effect of Quranic Recitation and Classical Music on Pain Intensity and Interleukin-6 Levels After Lower Limb Orthopedic Surgery With Intrathecal Anesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Muslim patients scheduled for elective lower extremity orthopedic surgery during the study period
- Aged 18 to 60 years
- Agree to participate in the study
- Undergoing lower extremity orthopedic surgery (ORIF, OREF, or bone replacement) lasting at least 60 minutes
You will not qualify if you...
- Patients with consciousness disorders
- Patients with neurological disorders
- Patients with cognitive disorders
- Patients with more than 3 spinal attempts
- Patients with hearing impairments
- Body mass index (BMI) less than 18 or greater than 39 kg/m82
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 visit (in-person)
Duration - Surgery day plus 30 minutes post-surgery
Participants will undergo lower extremity orthopedic surgery with spinal anesthesia and will be randomly assigned to listen to murottal (Islamic verse recitation), classical music, or receive standard postoperative care during their recovery. Pain intensity and interleukin-6 levels will be assessed before and 30 minutes after surgery.
1 baseline visit and 1 follow-up visit on the day of surgery
Trial Site Locations
Total: 1 location
1
Prof. Dr. Margono Soekarjo Hospital
Purwokerto, Central Java, Indonesia, 53146
Actively Recruiting
Research Team
G
Guruh Perkasa, Doctor
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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