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Music Intervention During AEEP: A Prospective Randomized Controlled Trial

Effect of Music Intervention on Anxiety and Pain After Anatomical Endoscopic Enucleation of the Prostate: A Prospective Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07255118
Acronym
AEEP-MUSIC
Enrollment
135
Registered
2025-11-28
Start date
2023-09-01
Completion date
2025-03-01
Last updated
2025-11-28

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

Conditions

Anxiety, Benign Prostatic Hyperplasia, Postoperative Pain Management

Keywords

AEEP, Music type, Postopertive comfort, State Anxiety Inventory, Visual Analog Scale

Brief summary

This prospective randomized controlled study investigates the effect of perioperative music listening on anxiety and postoperative pain in patients undergoing Anatomical Endoscopic Enucleation of the Prostate (AEEP) for benign prostatic hyperplasia. A total of 135 patients were randomized into two parallel groups: 67 patients listened to relaxing instrumental music during the perioperative period, while 68 patients received standard care without music. Anxiety was assessed using the State Anxiety Inventory (SAI) immediately before surgery and 2 hours postoperatively, and pain was evaluated using the Visual Analog Scale (VAS) at the postoperative 2nd hour. The study aims to determine whether a simple, non-pharmacological behavioral intervention can improve perioperative patient comfort and recovery outcomes in endoscopic prostate surgery.

Detailed description

Benign prostatic hyperplasia (BPH) is one of the most common urological conditions in aging men, often requiring surgical intervention when medical therapy fails. Anatomical Endoscopic Enucleation of the Prostate (AEEP) has emerged as an effective and tissue-preserving surgical approach for managing BPH. Despite the minimally invasive nature of AEEP, perioperative anxiety and postoperative pain remain important determinants of patient comfort, satisfaction, and overall recovery. Music listening is a simple, inexpensive, and non-pharmacological behavioral intervention that has been shown in various surgical disciplines to reduce anxiety, modulate pain perception, and improve patient experience. However, its potential benefits during AEEP have not been previously explored. In this prospective randomized controlled trial, we evaluated the effect of perioperative music exposure on anxiety and acute postoperative pain among patients undergoing AEEP. A total of 135 male patients scheduled for AEEP were enrolled and randomized into two groups: Music Group (n = 67): Patients listened to standardized relaxing instrumental music via headphones starting immediately before anesthesia induction and continuing during the procedure. Control Group (n = 68): Patients received routine perioperative care without exposure to music. Perioperative anxiety was measured using the State Anxiety Inventory (SAI) at two predefined time points: immediately before surgery and at the postoperative 2nd hour. Postoperative pain intensity was assessed using the Visual Analog Scale (VAS) 2 hours after the procedure. All surgical and anesthetic techniques were standardized across groups to minimize variability. This study aims to determine whether perioperative music listening can serve as an effective adjunctive intervention to improve psychological well-being and reduce pain in patients undergoing AEEP. Findings from this research may support the integration of music into perioperative care pathways, offering a safe and easily applicable strategy to enhance patient-centered outcomes in endoscopic prostate surgery.

Interventions

BEHAVIORALMusic intervention

Patients listened to relaxing instrumental music beginning immediately before anesthesia induction and continuing throughout the procedure.

Sponsors

İrfan Şafak Barlas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

This is an open-label study. No parties were masked because the nature of the music intervention made blinding infeasible.

Intervention model description

Participants were randomly assigned to one of two parallel groups: a music intervention group receiving perioperative music listening via headphones, and a control group receiving standard perioperative care without music. Each participant received only the intervention allocated to his assigned group, and outcomes were compared between the two independent groups.

Eligibility

Sex/Gender
MALE
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* male patients aged ≥40 years * patients who underwent surgery under regional anesthesia without sedation * patients who did not benefit from medical treatment for BPO * preoperative International Prostate Symptom Score (IPSS) \>19 * preoperative maximum urine flow rate (Qmax) \<15 mL/sec * post-voiding residual volume (PVR) \>50 mL.

Exclusion criteria

* patients with urethral stricture * patients who underwent urological treatments other than laser enucleation of the prostate * patients with urinary tract infections and/or hematuria * patients with urinary system malignancy * patients with a history of previous prostate surgery * patients with neurogenic bladder * patients with hearing impairment * patients with psychiatric disorders or those using medications prescribed by a psychiatrist.

Design outcomes

Primary

MeasureTime frameDescription
Change in State Anxiety Inventory (SAI) ScoreFrom baseline (immediately before surgery) to postoperative 2nd hour.Perioperative anxiety will be measured using the State Anxiety Inventory (SAI) at two time points: immediately before surgery (baseline) and at 2 hours postoperatively. The outcome represents the change in SAI score between these two assessments.

Secondary

MeasureTime frameDescription
Postoperative Pain Score Assessed by Visual Analog Scale (VAS)Postoperative 2nd hour.Pain intensity will be evaluated using a 0-10 Visual Analog Scale (VAS) at the postoperative 2nd hour.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 12, 2026