- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05596877
Music Therapy in Pulmonary Rehabilitation
The Effect of Music Therapy on Anxiety and Perceived Time in Pulmonary Rehabilitation
Study Overview
Status
Conditions
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ke-Yun Chao, PhD
- Phone Number: +886-905-301-879
- Email: ck_qq@hotmail.com
Study Locations
-
-
-
New Taipei City, Taiwan, 24352
- Fu Jen Catholic University Hospital, Fu Jen Catholic University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
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
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
Sponsor
Investigators
- Principal Investigator: Ke-Yun Chao, PhD, Fu Jen Catholic University Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FJUH111237
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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