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Clinical Trials/NCT04159584
NCT04159584
Completed
Not Applicable

Pilot Study: The Effects of Medical Music on Anxiety in Patients With Interstitial Lung Disease

Weill Medical College of Cornell University1 site in 1 country10 target enrollmentApril 15, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Interstitial Lung Disease
Sponsor
Weill Medical College of Cornell University
Enrollment
10
Locations
1
Primary Endpoint
Feasibility of using a medical music intervention as a treatment for anxiety in subjects with ILD, as measured by descriptive evaluation.
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This is uncontrolled, interventional feasibility study for determining the effects medical music on anxiety levels in subjects with ILD. Enrolled subjects will be asked to complete questionnaires and undergo physiologic measurements prior to listening to medical music. The music intervention will be for approximately 30 minutes. Post intervention questionnaires and physiologic measurements will be done.

Detailed Description

The Medical Music intervention includes playlists that contains songs specifically designed, recorded, and optimized through the provisionally-patented methods, to treat their co-morbid anxiety. The duration of the medical music playlist is 30 minutes. Enrolled subjects will be asked to complete questionnaires to assess anxiety, a questionnaire related to their music preferences, and undergo physiological measurements (vital signs, galvanic skin response, and heart rate variability) before and after the intervention.

Registry
clinicaltrials.gov
Start Date
April 15, 2019
End Date
September 11, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Men and women age 50 to 80 years old
  • Diagnosis of definite or probable interstitial lung disease (ILD)
  • Willingness to participate and sign consent

Exclusion Criteria

  • Patients who are deaf
  • Inability to provide informed consent
  • Pregnant women

Outcomes

Primary Outcomes

Feasibility of using a medical music intervention as a treatment for anxiety in subjects with ILD, as measured by descriptive evaluation.

Time Frame: Baseline to 30 minutes

Secondary Outcomes

  • Change in State Anxiety Inventory scores before and after intervention(Baseline to 30 min)
  • Change in heart rate variability before and after intervention(Baseline to 30 min)
  • Change in Visual Analogue Scale scores for Anxiety and Distress (VAS-A) before and after intervention(Baseline to 30 min)
  • Change in Borg Dyspnea Scale scores before and after intervention(Baseline to 30 min)
  • Change in galvanic skin response before and after intervention(Baseline to 30 min)

Study Sites (1)

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