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Recruiting NCT07171008

NCT07171008 The Effect of Ney Music on Patients Undergoing Lumbar Disc Surgery

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Clinical Trial Summary
NCT ID NCT07171008
Status Recruiting
Phase
Sponsor Niran Çoban
Condition Lumbar Disc Herniation
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2025-04-01
Primary Completion 2025-12-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 70 Years
Study Type INTERVENTIONAL
Interventions
Ney music

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2025-04-01 with a primary completion date of 2025-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized controlled study aims to investigate the effects of ney music listening, a traditional Turkish wind instrument, on pain, anxiety, sleep quality, and vital signs in patients undergoing lumbar disc herniation surgery. Participants will be randomly assigned to intervention and control groups. The intervention group will receive a 15-minute ney music session at three different time points: preoperative (on the day of surgery), postoperative 3rd hour, and postoperative day 1. The control group will receive standard postoperative nursing care without music intervention. Data will be collected at the same time points in both groups using the Visual Analog Scale (VAS), State-Trait Anxiety Inventory (STAI-I), Richard-Campbell Sleep Questionnaire, and vital signs. The study seeks to evaluate the non-pharmacological benefits of therapeutic music in postoperative recovery.

Eligibility Criteria

Inclusion Criteria: * Having undergone lumbar disc surgery under general anesthesia * 18 years old and over, * At least 3 hours have passed from the analgesic administration, * Patients willing to participate in the study will be included in the study. Exclusion Criteria: * Patient-controlled analgesia (PCA) is applied, * Over 70 years old, * Using anxiolytic and sedative drugs, * Having a psychiatric illness, * Patients with communication barriers will not be included in the study.

Contact & Investigator

Central Contact

NİRAN ÇOBAN

✉ nirancoban@gmail.com

📞 05301586912

Principal Investigator

NİRAN ÇOBAN

STUDY DIRECTOR

University of Yalova

Frequently Asked Questions

Who can join the NCT07171008 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 70 Years, studying Lumbar Disc Herniation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07171008 currently recruiting?

Yes, NCT07171008 is actively recruiting participants. Contact the research team at nirancoban@gmail.com for enrollment information.

Where is the NCT07171008 trial being conducted?

This trial is being conducted at Yalova, Turkey (Türkiye).

Who is sponsoring the NCT07171008 clinical trial?

NCT07171008 is sponsored by Niran Çoban. The principal investigator is NİRAN ÇOBAN at University of Yalova. The trial plans to enroll 60 participants.

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