The Effect of Music Listening on Nursing Students

April 15, 2025 updated by: Teresa Lesiuk, University of Miami

The Effect of Sedative and Stimulative Music Listening on State-Anxiety, Heart Rate, and Galvanic Skin Response in Nursing Students

The purpose of this study is to explore the effect of sedative and stimulative music listening on physiological responses among nursing students.

Study Overview

Study Type

Interventional

Enrollment (Actual)

34

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Florida
      • Coral Gables, Florida, United States, 33146
        • University of Miami
      • Coral Gables, Florida, United States, 33146
        • University of Miami School of Nursing and Health Studies
      • Coral Gables, Florida, United States, 33146
        • Weeks Music Library and Technology Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria:

  • a senior, junior, or second-semester sophomore in the traditional undergraduate Bachelor of Science in Nursing (BSN) program
  • a student in the accelerated BSN program

Exclusion criteria:

•self-reported hearing impairments.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Sedative music followed by stimulative music group
The participants in this group will receive sedative music followed by stimulative music for up to 25 minutes each. Session two will occur two days after session one.
The participants will come twice in person and listen to 9 minutes of sedative music.
The participants will come twice in person and listen to 9 minutes of stimulative music.
Experimental: Stimulative music followed by sedative music group
The participants in this group will receive stimulative music followed by sedative music for up to 25 minutes each. Session two will occur two days after session one.
The participants will come twice in person and listen to 9 minutes of sedative music.
The participants will come twice in person and listen to 9 minutes of stimulative music.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Heart Rate
Time Frame: baseline, up to 12 minutes
Heart rate will be measured using the Polar Verity Sense Optical Heart Rate Sensor in beats per minute (bpm)
baseline, up to 12 minutes
Change in Skin Conductance
Time Frame: baseline, up to 12 minutes
Skin conductance will be measured using the NeuLog Galvanic Skin Response (GSR) in micro Siemens (µS).
baseline, up to 12 minutes
Change in Anxiety Level
Time Frame: baseline, up to 12 minutes
The Six Item State-Trait Anxiety Inventory includes six statements that are rated on a 4-point Likert scale (1=Not at all, 2=Somewhat, 3=Moderately so, 4=Very much). The scale will measure current feelings of anxiety.
baseline, up to 12 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Degree of Stress Experienced by A Nursing Student measured by the Perceived Stress Scale for Nursing Students (PSS) Likert Scale
Time Frame: up to 5 minutes
The PSS consists of 29 items that are rated on a 5-point Likert scale (1=Never, 2=Seldom, 3=Sometimes, 4=Often, 5=Always). The PSS measures the degree of stress experienced by a nursing student based on stressful factors relevant to the demanding nursing curriculum.
up to 5 minutes
Liking Song Scale (4-point Likert Scale)
Time Frame: up to 5 minutes
Each music playlist will consist of three songs. The participant will rate how much the participant liked each of the three songs on a 4-point Likert scale (1=Not at all, 2=Somewhat, 3=Moderately so, 4=Very much).
up to 5 minutes
Familiarity Song Scale (Rating scale)
Time Frame: up to 5 minutes
Each music playlist will consist of three songs. The participant will indicate how familiar the participant is with each of the three songs on a rating scale (0=No, 1= I'm not sure, 2=Yes). The results of each song will be added to represent a quasi-continuous variable for how familiar the participant was with the music playlist as a whole.
up to 5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Teresa Lesiuk, PhD, University of Miami

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 21, 2024

Primary Completion (Actual)

February 5, 2025

Study Completion (Actual)

February 5, 2025

Study Registration Dates

First Submitted

October 16, 2024

First Submitted That Met QC Criteria

October 16, 2024

First Posted (Actual)

October 17, 2024

Study Record Updates

Last Update Posted (Actual)

April 18, 2025

Last Update Submitted That Met QC Criteria

April 15, 2025

Last Verified

October 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 20241018

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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