Music Therapy in Pulmonary Rehabilitation

April 7, 2023 updated by: Ke-Yun, Chao, Fu Jen Catholic University

The Effect of Music Therapy on Anxiety and Perceived Time in Pulmonary Rehabilitation

This study explores the effects of music therapy intervention on anxiety and time perception during pulmonary rehabilitation.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Background:

In recent years, in many domestic and foreign music therapy literature, it can be found that the intervention of music therapy can alleviate the anxiety of patients in the treatment, surgery, and even patients with critical care using ventilators, and then affect the patient's physiological indicators, in addition, there are also studies that mention that background music affects people's waiting time perception, reduces people's waiting time, can reduce the generation of negative emotions, and improve the quality of hospital medical care. The objective of this study was to explore the effects of music therapy on anxiety and time perception during pulmonary rehabilitation.

Study Design:

This case is a one-year single-center, prospective block randomizied trial.

Methods:

The study is expected to be 50 people, randomly assigned to two groups (control group, experimental group) will be carried out in the pulmonary rehabilitation room on the sixth floor of the Fu Jen Catholic University Hospital, using the Baker Anxiety Scale, physiological monitoring instruments and cardiac output monitor as tools to test the effects of anxiety sensations, physiological responses (heartbeat, breathing times, blood pressure, heart rate variability) and perceptual time in two situations of interventional music therapy and non-interventional music therapy during the rehabilitation of negative pressure respirators.

Effect:

It was mainly found that the intervention of music therapy can reduce anxiety, number of heartbeats, number of breaths and blood pressure, and shorten the perceptual time of patients with pulmonary rehabilitation.

Key words:

Music therapy; pulmonary rehabilitation; depression; percieved time; chronic obstructive pulmonary disease

Study Type

Interventional

Enrollment (Actual)

50

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 Contact

Study Locations

      • New Taipei City, Taiwan, 24352
        • Fu Jen Catholic University Hospital, Fu Jen Catholic University

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

20 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Recieved pulmonary rehabilitation at least three months
  • Recieved a negative ventilation during a pulmonary rehabilitation
  • A written informed consent

Exclusion Criteria:

  • impaired of hearing
  • decline to participate
  • cognitive communication deficits
  • acute exacerbation of copd within three months

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Group
Recieved pulmonary rehabilitation
Experimental: Intervention Group
Recieved pulmonary rehabilitation with music therapy
Performing music therapy during a course of pulmonary rehabilitation (25 mins)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Beck Anxiety Inventory's score
Time Frame: 25 minutes
Beck Anxiety Inventory's score (0 present as minimal and 63 present as maximal, higher scores mean a worse outcome)
25 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Respiratory rate
Time Frame: 25 minutes
Respiratory rate during a course of pulmonary rehabilitation
25 minutes
Heart rate variability
Time Frame: 25 minutes
Heart rate variability during a course of pulmonary rehabilitation
25 minutes

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Ke-Yun Chao, PhD, Fu Jen Catholic University Hospital

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)

November 21, 2022

Primary Completion (Actual)

February 11, 2023

Study Completion (Actual)

February 11, 2023

Study Registration Dates

First Submitted

October 24, 2022

First Submitted That Met QC Criteria

October 24, 2022

First Posted (Actual)

October 27, 2022

Study Record Updates

Last Update Posted (Actual)

April 10, 2023

Last Update Submitted That Met QC Criteria

April 7, 2023

Last Verified

December 1, 2022

More Information

Terms related to this study

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

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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