Three Distraction Methods for Pain Reduction During Cystoscopy: A Randomized Controlled Trial Evaluating the Effects on Pain, Anxiety, and Satisfaction.
Elif Gezginci, Emine Iyigun, Yusuf Kibar...
https://pubmed.ncbi.nlm.nih.gov/30280915Actively Recruiting
Phase Not Applicable
Age: 18Years - 70Years
All Genders
Healthy Volunteers
ID07171008
The Effect of Ney Music on Pain, Anxiety, Sleep, and Quality of Life in Patients Undergoing Lumbar Disc Surgery
Led by Niran Çoban · Updated on 2025-11-25
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the effects of ney music, a traditional Turkish wind instrument, on pain, anxiety, sleep quality, and vital signs in patients undergoing lumbar disc herniation surgery. The trial investigates whether listening to ney music can support postoperative recovery by reducing discomfort and improving physiological parameters. It is a randomized controlled study designed to explore non-drug supportive methods in surgical care. Participants will be randomly assigned to either an intervention group or a control group. The intervention group will listen to 15-minute sessions of ney music at three specific times: before surgery on the day of the operation, three hours after surgery upon transfer to the clinic, and the morning of the first day after surgery. The control group will receive standard postoperative nursing care without any music intervention. Both groups will have measurements taken at these times for comparison. During the study, researchers will assess pain using the Visual Analog Scale, anxiety with the State-Trait Anxiety Inventory, sleep quality through the Richard-Campbell Sleep Questionnaire, and vital signs including blood pressure, pulse, and oxygen saturation before and after each music session in the intervention group. Similar assessments will be made in the control group without music. The study's outcomes will be reviewed over six months to understand the impact of ney music on recovery. Participants will attend scheduled sessions around their surgery and follow-up assessments.
CONDITIONS
Brief Title
The Effect of Ney Music on Patients Undergoing Lumbar Disc Surgery
Who Can Participate
Age: 18Years - 70Years
All Genders
Healthy Volunteers
Eligibility Criteria
You may qualify if you...
- Having undergone lumbar disc surgery under general anesthesia
- 18 years old and over
- At least 3 hours have passed since analgesic administration
- Willingness to participate in the study
You will not qualify if you...
- Use of patient-controlled analgesia (PCA)
- Over 70 years old
- Using anxiolytic or sedative drugs
- Having a psychiatric illness
- Communication barriers preventing participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
1
2
3
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Surgery
Duration - 1 day
Participants undergo lumbar disc surgery under general anesthesia.
1 day of hospital stay for surgery
Treatment
Duration - From the evening before surgery through the morning of the first day after surgery
Participants in the intervention group listen to 15 minutes of ney music in a quiet, dimly lit environment at three specific times: the evening before surgery, within 3 hours after surgery, and the morning of the first day after surgery. Pain, anxiety, sleep quality, and vital signs are assessed before and after each session. Participants in the control group receive routine postoperative care without music but have the same assessments at the same time points.
3 sessions of music listening and assessments
Post-operative Follow-up
Duration - 6 months
Participants are observed for recovery outcomes related to pain, anxiety, sleep quality, and physiological parameters over a 6-month period.
Periodic assessments during follow-up
Trial Site Locations
Total: 1 location
1
Niran Çoban
Yalova, Turkey (Türkiye), 77000
Actively Recruiting
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Research Team
N
NİRAN ÇOBAN
S
Sena Battal
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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