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NCT03327077 Clinical Trial

Music in Urgent and Emergent Settings

Musculoskeletal Pain Clinical Trial

— MUES III  

Official title:
Music in Urgent and Emergent Settings (MUES) Trial: Phase Three

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03327077
Other study ID # IRB201700938
Secondary ID 15-3800-7018
Status Completed
Phase N/A
First received
Last updated
Start date October 30, 2017
Est. completion date March 31, 2019

Study information
Verified date March 2020
Source University of Florida
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to study the impact of Live Preferential Music on the patient perception of pain and management of pain syndromes in the ED.

Description:

The purpose of this study is to study the impact of Live Preferential Music on the patient perception of pain and management of pain syndromes in the ED. This study follows a prospective experimental design where patients will be assigned to two groups: one that receives the music intervention and one that does not receive music intervention.

Recruitment information / eligibility
Status Completed
Enrollment 304
Est. completion date March 31, 2019
Est. primary completion date March 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

1. Age: =18

2. Chief complaint of musculoskeletal pain

3. Gender: Male or Female

4. Ethnicity: Any

5. Physical ability: Any

6. Language: English

7. Cognitive skill/education: grade 2 reading level or above

8. Physically and cognitively able to participate in study procedures

Exclusion Criteria:

1. Patients who are unable to participate in the informed consent process

2. Prisoners

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Live Preferential Music
Trained musicians will play live preferential music to ED patients who consent to participate.

Locations
Country Name City State
United States Unversity of Florida Gainesville Florida

Sponsors (2)
Lead Sponsor Collaborator
University of Florida US National Endowment for the Arts

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain reduction 60 to 90 minutes
Secondary Cost of care 20 weeks
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