Effect Of Musıc Therapy On Anxıety Levels In COVID-19 Pandemıc

December 16, 2023 updated by: Saadet Can Çiçek, Abant Izzet Baysal University

Effect Of Musıc Therapy On Anxıety Levels In Prımary Care Famıly Health Workers In COVID-19 Pandemıc

This study, which has a randomized controlled experimental design, was planned to determine the effect of music therapy on the anxiety level of family health personnel working in primary health care centers during the COVID-19 pandemic. The study will be carried out between 4 August and 31 December with nurses, midwives and other family health personnel working in family health centers. Participants will be randomized into two groups, a control and an intervention group. Individuals in the intervention group will receive 15 minutes of music therapy once a day for 5 days. No intervention will be made in the control group. Data Descriptive Question and State-Trait Anxiety Inventory online design; It will be collected on the Google Forms platform.. Data analysis will be done using SPSS 20 program.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Today, billions of people are struggling with the pandemic caused by the COVID-19 virus. The pandemic causes many psychosocial and mental health problems in humans. (Montano and Acebes 2020, Guo, Feng et al. 2020, Ostacoli, Cosmo et al. 2020, Carmassi, Foghi et al. 2020, Heitzman 2020, Sun, Sun et al. 2021, Yuan ,Gong et al. 2021, Taylor, Landry et al 2020 ). Many people have faced problems such as stress, depression and anxiety (Liu, Yang et al 2020). Compared to other segments of the society, health workers experience these problems more frequently and more severely. The reason for this is that healthcare professionals undertake the task of providing health care services to people infected with the virus, being together with patients, having close contact and meeting their health needs. This situation triggers the risk of contact with patients, fear of death, concerns about the health of themselves and their family members, and psychological problems (Aykurt and Aykurt 2020). Therefore, healthcare workers are considered to be a high-risk group in which the psychological consequences of COVID-19 are significant and persistent (Fiorillo and Gorwood 2020).

Studies in the literature have shown that healthcare workers experience severe anxiety due to COVID-19. (Yanez, Jahanshahi et al 2020, Sahebi, Nejati et al 2021, Lai, Ma et al 2019, Ataç, Sezerol et al 2020, Luo, Liu et al 2021).

It is very important to screen health workers who provide uninterrupted service in pandemic conditions in terms of anxiety and other psychological problems and to plan remedial interventions. In this context, music therapy, which is known as an effective method to reduce the anxiety level of individuals and reduce stress, comes to mind. Music therapy studies with healthcare professionals are limited in the literature. In this context, it is aimed that this study will contribute to filling this gap in the literature and creating a database.

Study Type

Interventional

Enrollment (Estimated)

42

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 Contact Backup

Study Locations

      • Bolu, Turkey
        • Recruiting
        • Family Health Centers in Bolu
        • Contact:
          • ASM

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Not having a verbal or auditory communication barrier,
  • To voluntarily agree to participate in the research,
  • Not having a diagnosis of neuropsychiatric disease,
  • Having the opportunity to fill out the surveys online,
  • Possess the title of midwife or nurse.

Exclusion Criteria:

  • Having a diagnosed neuropsychiatric disorder,
  • Verbal and auditory communication disability,
  • Not being willing to participate in the research,
  • Having a title other than a midwife or nurse.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group

4 music genres with expert opinion will be presented to the preference of the participants in the intervention group, these types of music; Classical Music, Turkish Classical Music, Turkish Folk Music and Sufi Music. The music is instrumental, 70 decibels and non-verbal. Participants will listen to a genre they choose and download to their mobile phones once for 5 days for 15 minutes. They will listen to the music in the environment they live in, at a time convenient for them, at the desired volume level and with headphones in accordance with the determined therapy program.

At the beginning of the research, an Introductory Questionnaire will be applied to all participants. Trait Anxiety Inventory will be administered before music therapy on the 1st day of the study and after the music therapy application on the 5th day.

Classical Music, Turkish Classical Music, Turkish Folk Music and Sufi Music
No Intervention: Control group
No application will be made to the participants in the control group, and the data collection tools will be applied with the same frequency as in the intervention group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anxiety
Time Frame: Two months

State-Trait Anxiety Scale

The scale consists of a total of 40 items in two separate parts. The scale includes direct and reversed statements. The total score that can be obtained from the scale is a minimum of 20 and a maximum of 80 points, and an increase in the score indicates an increase in the level of anxiety (Öner and Le Compte 1983).

Two months

Collaborators and Investigators

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

Investigators

  • Study Director: Saadet CAN ÇİÇEK, http://www.ibu.edu.tr/tr

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)

December 8, 2021

Primary Completion (Estimated)

January 31, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

July 30, 2021

First Submitted That Met QC Criteria

July 30, 2021

First Posted (Actual)

August 3, 2021

Study Record Updates

Last Update Posted (Actual)

December 19, 2023

Last Update Submitted That Met QC Criteria

December 16, 2023

Last Verified

December 1, 2023

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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