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Personalized Music for Anxiety During Cataract Surgery

The Effect of Music Selected According to Patients' Musical Preferences on Anxiety and Pain During Cataract Surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07767643
Enrollment
100
Registered
2026-08-17
Start date
2023-09-11
Completion date
2024-05-06
Last updated
2026-08-19

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

Conditions

Anxiety, Cataract, Pain

Keywords

Cataract Surgery, Personalized Music, Music Intervention, Anxiety, Pain, Perioperative Nursing

Brief summary

This randomized controlled trial evaluated the effect of a personalized music intervention on anxiety and pain in patients undergoing cataract surgery under local anesthesia. A total of 100 patients were randomly assigned to an intervention group or a control group. Patients in the intervention group received a structured personalized music intervention during surgery based on their musical preferences, while patients in the control group received standard care. Anxiety was assessed before and immediately after surgery using the State-Trait Anxiety Inventory-State (STAI-S), and pain was assessed immediately after surgery and two hours after surgery using the Visual Analog Scale (VAS). The study aimed to determine whether personalized music provided during cataract surgery could reduce patients' anxiety and pain compared with standard care.

Interventions

BEHAVIORALStructured Personalized Music Intervention

Participants received a structured personalized music intervention during cataract surgery. Music was individualized according to participant preferences using a structured assessment of music preferences. Instrumental music with a tempo of approximately 60-100 beats per minute was selected and delivered in the operating room for approximately 30 minutes during surgery, in addition to standard perioperative care.

Sponsors

Ege University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

Due to the nature of the intervention, participants, care providers, and outcome assessors were not blinded to group allocation.

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Aged 40-75 years * Able to read and write * Able to speak and understand Turkish * No psychiatric or neurological diagnosis that could affect pain or anxiety * Willing to participate in the study

Exclusion criteria

* Communication problems * Communication impairment * Chronic pain * Psychiatric disorder * Substance or alcohol dependence * History of ear infection * Previous ocular surgery other than cataract surgery * Mature cataract, traumatic cataract, or other conditions considered likely to prolong surgery or increase the risk of complications * Complicated diabetes mellitus (polyneuropathy, diabetic retinopathy, or nephropathy) or HbA1c ≥8% (uncontrolled diabetes)

Design outcomes

Primary

MeasureTime frameDescription
State Anxiety Level Assessed Using the State-Trait Anxiety Inventory-State (STAI-S)Approximately 1 hour before surgery and immediately after surgeryState anxiety was assessed using the 20-item State-Trait Anxiety Inventory-State (STAI-S), with total scores ranging from 20 to 80. Higher scores indicate greater levels of state anxiety. STAI-S was administered approximately 1 hour before surgery and immediately after surgery to evaluate perioperative state anxiety.

Secondary

MeasureTime frameDescription
Pain Intensity Assessed Using the Visual Analog Scale (VAS)Immediately after surgery and 2 hours after surgeryPain intensity was assessed using the Visual Analog Scale (VAS), ranging from 0 (no pain) to 10 (worst possible pain), with higher scores indicating greater pain intensity. Pain was assessed immediately after surgery and 2 hours after surgery to evaluate postoperative pain.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORKübra Yigit Gökbel, MSc

Ege University, Faculty of Nursing

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 20, 2026