NCT07518953

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
5mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress45%
Apr 2026Jan 2027

First Submitted

Initial submission to the registry

April 1, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

April 9, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2027

Last Updated

April 13, 2026

Status Verified

April 1, 2026

Enrollment Period

9 months

First QC Date

April 1, 2026

Last Update Submit

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

EXPERIMENTAL

Participants listen to a standardized instrumental/classical/relaxing music playlist beginning 2-3 minutes before local anesthesia and continuing throughout the nail biopsy procedure.

Behavioral: Music interventionProcedure: Local anesthesia injections

Standard care/ control

OTHER

Participants receive standard care during nail biopsy without any music intervention. No music is played during local anesthesia administration or the procedure.

Procedure: Local anesthesia injections

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.

Music Intervention

Local anesthesia injections

Music InterventionStandard care/ control

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Shari R Lipner, MD, PhD

    Weill Cornell Medicine, Department of Dermatology

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Shari R Lipner, MD, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: Two parallel arms: music intervention group and standard care control group, randomized 1:1.
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

Locations