The Effect of Progressive Relaxation Exercise With Music Therapy on Sleep Quality and Pain Intensity

September 5, 2023 updated by: Pınar Duru, Eskisehir Osmangazi University

The Effect of Progressive Relaxation Exercise With Music Therapy on Sleep Quality and Pain Intensity of Patients Hospitalized in Surgical Services

This study was conducted to determine the effect of progressive relaxation exercises with music therapy on sleep quality and pain severity of patients hospitalized in the surgical departments of a university hospital.This single-blind, pre-test-post-test with control group design quasi-experimental study was carried out between March-July 2019. 31 patients who were hospitalized in surgical departments for at least one week and regularly performed relaxation exercises consisted of experimental group, and 31 patients who were hospitalized for at least one week but did not do relaxation exercises consisted of control group. The study data were collected by using "Descriptive Characteristics Form", pain severity of patients was measured using "Visual Analogue Scale", and sleep quality of patients was measured using "Visual Analogue Sleep Scale". The patients were asked to perform the exercises with music an average of 30 min before sleeping every day for a week. The observation of the nurse working in department and the patient's statement were used for control. The ethical permission and the approval of hospital management were obtained for the study. In the statistical analysis of the data, independent sample t test, one-way anova and paired sample t test were used. Statistical significance level was taken as p<.05.

Study Overview

Detailed Description

Inclusion criteria in the study:

  • Agree to participate in research
  • Staying in surgical wards for at least one week between the dates of the study
  • Being 18 years or older
  • Not regularly practicing relaxation exercises before

Exclusion criteria from the study:

  • Refusing to participate in research
  • Being discharged before one week after admission to surgical services within the range of the study date
  • Those who are hospitalized for more than a week due to the possibility of serious illness diagnoses that prevent patients from performing relaxation exercises
  • Being 18 years or younger
  • Communication problem
  • Regularly practicing previous relaxation exercises

Study Type

Interventional

Enrollment (Actual)

62

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 Locations

    • Odunpazarı
      • Eskişehir, Odunpazarı, Turkey, 26040
        • Eskişehir Osmangazi University Practice and Research Hospital

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Agreeing to participate in research
  • Lying in surgical wards for at least a week in the range of the date of the study
  • Being 18 or older
  • Don't practice relaxation exercises regularly before

Exclusion Criteria:

  • Not agreeing to participate in research
  • Discharge before a week after admission to surgical wards within the range of the date of the study
  • Those with more than a week's sleep due to the likelihood that patients may have received serious disease diagnoses that would put them off doing relaxation exercises
  • Being 18 and under
  • Don't be a communication problem
  • Practice relaxation exercises regularly before

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: Other
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: intervention arm

Data from the study was collected during the implementation of the "Nursing Surgical Diseases" class. Students who completed the 4-hour training program on sleep, relaxation exercises and survey practice have been pollsters of the study.

Relaxing music for sleep, prepared by the Turkish Psychological Association, is uploaded to patients' mobile phones. Patients were asked to perform relaxation exercises for a week at bedtime, lasting an average of 30 minutes, and with music every day, taking advantage of nurse observation at the clinic with the patient's declaration in check. Students who took part in the practice served as reminders of patients' compliance with the exercises.

The progressive relaxation technique includes exercises for the muscles in the body to consciously contract and relax together with deep breathing exercises while sitting comfortably or lying down accompanied by music.

Relaxing relaxation music for sleep, prepared by the Turkish Psychologists Association, has been installed on the mobile phones of the patients.

The patients did the relaxation exercises for an average of 30 minutes before going to bed for a week and every day with music.Relaxing relaxation music for sleep, prepared by the Turkish Psychologists Association, has been installed on the mobile phones of the patients.

The patients were taught to do the relaxation exercises for an average of 30 minutes before going to bed for a week and every day with music.

Other: Control arm
Those who did not do progressive muscle relaxation exercises or did not practice regularly for a week constituted the control group.

The progressive relaxation technique includes exercises for the muscles in the body to consciously contract and relax together with deep breathing exercises while sitting comfortably or lying down accompanied by music.

Relaxing relaxation music for sleep, prepared by the Turkish Psychologists Association, has been installed on the mobile phones of the patients.

The patients did the relaxation exercises for an average of 30 minutes before going to bed for a week and every day with music.Relaxing relaxation music for sleep, prepared by the Turkish Psychologists Association, has been installed on the mobile phones of the patients.

The patients were taught to do the relaxation exercises for an average of 30 minutes before going to bed for a week and every day with music.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
postoperative pain
Time Frame: In two groups, pain intensity pre-test and post-test values were measured with Visual Analog Scale. Pre-tests were evaluated in the first hour of their arrival in the service. Post-tests were measured at 09.00 in the morning on the 7th postoperative .
Incision site pain experienced after surgery
In two groups, pain intensity pre-test and post-test values were measured with Visual Analog Scale. Pre-tests were evaluated in the first hour of their arrival in the service. Post-tests were measured at 09.00 in the morning on the 7th postoperative .
postoperative sleep quality
Time Frame: In two groups, sleep quality pre-test and post-test values were measured with Visual Analog Sleep Scale. Pre-tests were applied before the surgery. Post-tests were measured at 09.00 in the morning on the 7th postoperative
Quality of sleep in hospital stay
In two groups, sleep quality pre-test and post-test values were measured with Visual Analog Sleep Scale. Pre-tests were applied before the surgery. Post-tests were measured at 09.00 in the morning on the 7th postoperative

Collaborators and Investigators

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

Investigators

  • Study Chair: Özlem Örsal, Dr., ESOGUOU
  • Study Chair: Nedime Köşgeroğlu, Dr., Istanbul Rumeli University

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)

March 1, 2019

Primary Completion (Actual)

June 15, 2019

Study Completion (Actual)

July 31, 2019

Study Registration Dates

First Submitted

March 28, 2021

First Submitted That Met QC Criteria

March 30, 2021

First Posted (Actual)

April 1, 2021

Study Record Updates

Last Update Posted (Actual)

September 7, 2023

Last Update Submitted That Met QC Criteria

September 5, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 25403353-050.99-E.27718

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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