Effect of Music on Pain and Anxiety During Nail Biopsies
1 other identifier
interventional
30
1 country
1
Brief Summary
This study is looking at whether listening to music during a nail biopsy can reduce pain and anxiety. Patients scheduled for a nail biopsy at the Weill Cornell Medicine dermatology clinic will be randomly assigned to either listen to a calming instrumental/classical music playlist during their procedure or receive standard care without music. After the procedure, participants will complete short questionnaires rating their pain, anxiety, and overall satisfaction. The goal is to determine whether a simple, low-cost music intervention can improve the experience of patients undergoing nail biopsies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 1, 2026
CompletedStudy Start
First participant enrolled
April 1, 2026
CompletedFirst Posted
Study publicly available on registry
April 9, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2027
April 13, 2026
April 1, 2026
9 months
April 1, 2026
April 8, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Mean pain intensity measured by Visual Analog Scale
Total scores range from 0-10 with 10 meaning worst pain imaginable
Immediately after the nail biopsy procedure
Secondary Outcomes (6)
Mean anxiety score measured by short-form State-Trait Anxiety Inventory
Immediately after the nail biopsy procedure
Perceived helpfulness of music intervention (music group only) measured by single-item Likert scale
Immediately after the nail biopsy procedure
Patient satisfaction score measured by single-item Likert scale rating overall experience
Immediately after the nail biopsy procedure
Willingness to undergo future nail biopsy procedures measured by single-item yes/no question
Immediately after the nail biopsy procedure
Number of participants with adverse events related to the procedure
immediately after the nail biopsy procedure
- +1 more secondary outcomes
Study Arms (2)
Music Intervention
EXPERIMENTALParticipants listen to a standardized instrumental/classical/relaxing music playlist beginning 2-3 minutes before local anesthesia and continuing throughout the nail biopsy procedure.
Standard care/ control
OTHERParticipants receive standard care during nail biopsy without any music intervention. No music is played during local anesthesia administration or the procedure.
Interventions
A standardized playlist of instrumental, classical, and relaxing music delivered to participants beginning 2-3 minutes before local anesthesia administration and continuing throughout the nail biopsy procedure. The music is intended to reduce procedural pain and anxiety as an adjunct to standard care.
Local anesthesia injections
Eligibility Criteria
You may qualify if:
- Male or female ≥18 years of age
- Scheduled to undergo nail biopsy at the Weill Cornell Medicine dermatology clinic
- Able to provide informed consent
- Able to read and understand English
You may not qualify if:
- Significant hearing impairment that would prevent ability to hear the music intervention
- Cognitive impairment that would prevent completion of study questionnaires
- Unable or unwilling to provide informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Weill Cornell Medicine Department of Dermatology
New York, New York, 10021, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Shari R Lipner, MD, PhD
Weill Cornell Medicine, Department of Dermatology
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 1, 2026
First Posted
April 9, 2026
Study Start
April 1, 2026
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
January 1, 2027
Last Updated
April 13, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share