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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05334641
Other study ID # InonuGYKoca001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 3, 2020
Est. completion date June 30, 2020

Study information

Verified date April 2022
Source Inonu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Introduction: This study has been conducted to determine the effect of music on pain and anxiety levels in patients receiving chemotherapy during COVID-19. Methods: The research has been carried out in a real trial model with adult patients receiving chemotherapy. The sample of the study is consisted of 92 patients (45 in the experimental group and 47 for the control group). The data have been collected by the researcher with Google Forms (using State and Transient Anxiety Inventory and Visual Analog Skala) between March 2020 and July 2020, through the links sent to the phones of participants on the day they received chemotherapy. Results: The mean scores obtained from the post-test STAI (53.11±4.77) and VAS (3.44±2.53) scales in the experimental group have been determined to statistically significantly decrease when compared to the pre-test measurement data (STAI:54.26±4.26; VAS:4.22±2.41) (p<0.05). No statistically significant difference has been determined between pre-test and post-test mean scores of the patients in the control group. Conclusion: It has been observed that music applications reduce the pain and anxiety levels of patients receiving chemotherapy during the COVID-19 process. It can be recommended to use music applications in the management of pain and anxiety symptoms.


Recruitment information / eligibility

Status Completed
Enrollment 92
Est. completion date June 30, 2020
Est. primary completion date June 29, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Over the age 18, - Being able to communicate, - Being literate, - Having no diagnosis of psychiatric, - Have the necessary technological equipment (phone, internet, etc.) Exclusion Criteria: - Existing infection - Receiving palliative chemotherapy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Listening Music
The patients in the experimental group were listened to music.
Not Listening Music
The control group was not listened to music.

Locations

Country Name City State
Turkey Vocational School of Health Services Malatya

Sponsors (1)

Lead Sponsor Collaborator
Inonu University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Google Forms (using State and Transient Anxiety Inventory and Visual Analog Skala) The data have been collected by the researcher with Google Forms (using State and Transient Anxiety Inventory and Visual Analog Skala).The posttest was administered 1 hour after the pretest. The posttest was administered 1 hour after the pretest.
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