Effects of Music Therapy on Procedural Pain, Anxiety and Comfort Level During Cystoscopy

June 1, 2020 updated by: Hanife DURGUN, T.C. ORDU ÜNİVERSİTESİ

A Randomized Controlled Trial on the Effects of Music Therapy on Procedural Pain, Anxiety and Comfort Level During Cystoscopy

Aims and objectives: This study aimed to determine the effect of music therapy on procedural pain intensity and anxiety and comfort levels in patients during cystoscopy.

Background: Cystoscopy is a procedure that is commonly performed as day surgery in urology clinics in order to diagnose lower urinary tract system symptoms as well as to diagnose and follow up tumors associated with the lower urinary system. During cystoscopy, which is an invasive intervention, individuals may experience pain and anxiety, and their comfort may be negatively affected.

Methods: This study was a prospective, randomized controlled trial. Study participants were randomly assigned to either a control or music group. The outcome measures were assessed using the Visual Analogue Scale, State Anxiety Scale, and General Comfort Questionnaire. This report followed the CONSORT checklist.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

  1. INTRODUCTION Cystoscopy is a common procedure in urology clinics and has two types: flexible and rigid. Especially recently, there has been an increase in the use of flexibles. Both of these types can be preferred as a diagnostic procedure in hematuria, atypical dysuria, bladder and upper urinary tract cancers, and suspected urethral stenosis. Rigid cystoscopy can be more painful than flexible cystoscopy.
  2. BACKGROUND Cystoscopy is a procedure performed in urology clinics to evaluate the lower urinary tract for a large number of symptoms and pathologies, but it is painful and causes anxiety in individuals. It is recommended to perform local anesthesia to the patients during the procedure, to select appropriate cystoscopy equipment, and to make the necessary environmental arrangements in order to reduce the patients' pain and anxiety and increase their comfort levels.

Environmental arrangements to manage interventional pain in cystoscopy include music therapy that has recently been used widely.Music is used as one of the complementary therapies in the treatment of many diseases due to its physical, psychological, and functional effects on individuals. The use of music as therapy in hospitals began to become widespread with the beginning of the world wars, but the introduction of pharmacological methods for the treatment of pain and anxiety has reduced the popularity of music in this context. With the identification of side effects of drugs in the subsequent years, starting again to use music as complementary therapy has come to the fore.

Music therapy in nursing first started in the 1800s with Florence Nightingale. Nightingale described music as an effective method in the recovery process in order to provide and increase patient comfort and reduce their anxiety levels. Music therapy has also been accepted as part of nursing practices within the scope of Nursing Interventions Classification.

In the literature, international studies have been conducted to reduce the pain and anxiety levels of individuals and increase their comfort levels. Considering two systematic reviews related to the subject;some studies noted that music played during flexible cystoscopy did not reduce pain and anxiety, while some studies stated that music could be effective in reducing pain and anxiety during cystoscopy. Controversial results were found in these two studies, which have high evidence levels. Experimental studies with control groups showed that music reduced pain and anxiety and increased comfort levels in patients undergoing flexible cystoscopy. Given the limitations of the studies on the subject and sample power/deficiencies, it may be observed that controversial conclusions have been reached about the effectiveness of music in relieving pain and anxiety. On the other hand, only one study has been found in Turkey regarding this issue. In a study, the effects of various distraction methods applied during the cystoscopy procedure (group 1: music, group 2: stress ball, group 3: video, and group 4: control) on pain, anxiety, and satisfaction were examined. The study found that the patients in the video group had lower pain and anxiety levels than those in the other groups. Considering the national and international studies available in the literature, regarding the topic of music therapy that may be effective in reducing pain and anxiety during the cystoscopy procedure, it is necessary to conduct further studies that provide high levels of evidence and produce scientific knowledge with greater sample sizes and by using randomized-controlled trials that are fundamental in assessing the effectiveness of evidence-based practices. This study aimed to determine the effect of music therapy on procedural pain intensity and anxiety and comfort levels in patients during cystoscopy.

2.1. Study hypotheses Hypothesis 1. Music therapy reduces procedural pain in patients during cystoscopy.

Hypothesis 2. Music therapy reduces anxiety in patients during cystoscopy. Hypothesis 3. Music therapy increases comfort level in patients during cystoscopy.

Study Type

Interventional

Enrollment (Actual)

72

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

      • Giresun, Turkey
        • Giresun 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

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion criteria:

  • Patients older than 18 years,
  • Being literate,
  • Having no hearing problems.

Exclusion criteria:

  • Patients who had allergies to anesthetic drugs
  • Urinary tract infection.

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: SUPPORTIVE_CARE
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
NO_INTERVENTION: control group
EXPERIMENTAL: a music group
Patients in the music group were provided music therapy that was prepared by the Turkish Psychological Association. They listened to the music that has a calming and relaxing effect for 20 min before and during the procedure.

Patients in the music group were provided music therapy that was prepared by the Turkish Psychological Association. They listened to the music that has a calming and relaxing effect for 20 min before and during the procedure.

A portable MP3 player connected to double earphones was used in the present study. After patients took the lithotomy position for cystoscopy, their headphones were inserted and music began to be played. Music was played to the individuals for 20 minutes before and during the procedure. Headphones were removed immediately after the procedure was completed and the double earphones were cleaned with antiseptic solution after each application.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain scores
Time Frame: before cystoscopy
The primary outcome of the study was to measure pain using a 10-cm VAS, with high numbers meaning greater pain intensity. The VAS is used to measure various subjective clinical phenomena, including pain. It is quick and easy to use and score. The 0-10 VAS requires the patients to choose a number from 0 to 10 that best represents their pain; 0 is the equivalent of "no pain," and 10 is the equivalent of the worst imaginable pain
before cystoscopy
Pain scores
Time Frame: during cystoscopy procedure
The primary outcome of the study was to measure pain using a 10-cm VAS, with high numbers meaning greater pain intensity. The VAS is used to measure various subjective clinical phenomena, including pain. It is quick and easy to use and score. The 0-10 VAS requires the patients to choose a number from 0 to 10 that best represents their pain; 0 is the equivalent of "no pain," and 10 is the equivalent of the worst imaginable pain
during cystoscopy procedure
Pain scores
Time Frame: immediately after cystoscopy procedure is completed
The primary outcome of the study was to measure pain using a 10-cm VAS, with high numbers meaning greater pain intensity. The VAS is used to measure various subjective clinical phenomena, including pain. It is quick and easy to use and score. The 0-10 VAS requires the patients to choose a number from 0 to 10 that best represents their pain; 0 is the equivalent of "no pain," and 10 is the equivalent of the worst imaginable pain
immediately after cystoscopy procedure is completed
Anxiety score
Time Frame: before cystoscopy
Anxiety was used as the secondary outcome and measured using the Turkish version of the State-Trait Anxiety Inventory (STAI). The inventory was developed by Spielberger and colleagues and tested for its validity and reliability in Turkish by Öner and Le Compte. Its internal consistency, test-retest reliability, and item-by-item reliability values were found to be between 0.83 and 0.87, 0.71 and 0.86, and 0.34 and 0.72, respectively. The STAI consists of a State Anxiety Scale (STAI-S) and a Trait Anxiety Scale (STAI-T). Only the STAI-S was used in this study. The lowest total score that can be obtained from the scale is 20, and the highest total score is 80. A high score indicates high anxiety level, and a low score indicates low anxiety level
before cystoscopy
Anxiety score
Time Frame: immediately after cystoscopy procedure is completed
Anxiety was used as the secondary outcome and measured using the Turkish version of the State-Trait Anxiety Inventory (STAI). The inventory was developed by Spielberger and colleagues and tested for its validity and reliability in Turkish by Öner and Le Compte. Its internal consistency, test-retest reliability, and item-by-item reliability values were found to be between 0.83 and 0.87, 0.71 and 0.86, and 0.34 and 0.72, respectively. The STAI consists of a State Anxiety Scale (STAI-S) and a Trait Anxiety Scale (STAI-T). Only the STAI-S was used in this study. The lowest total score that can be obtained from the scale is 20, and the highest total score is 80. A high score indicates high anxiety level, and a low score indicates low anxiety level
immediately after cystoscopy procedure is completed
Comfort scores
Time Frame: before cystoscopy
The third outcome was comfort, which was measured using the General Comfort Questionnaire (GCQ). This questionnaire was developed by Katharine Kolcaba to determine individuals' comfort needs and evaluate nursing interventions that may be employed to ensure and increase such comfort. The GCQ uses a four-point Likert-type scale and consists of 48 items. The lowest score that can be obtained when using the scale is 48, and the highest score is 192. The GCQ was adapted for use in a Turkish context by Kuğuoğlu and Karabacak.
before cystoscopy
Comfort scores
Time Frame: immediately after cystoscopy procedure is completed
The third outcome was comfort, which was measured using the General Comfort Questionnaire (GCQ). This questionnaire was developed by Katharine Kolcaba to determine individuals' comfort needs and evaluate nursing interventions that may be employed to ensure and increase such comfort. The GCQ uses a four-point Likert-type scale and consists of 48 items. The lowest score that can be obtained when using the scale is 48, and the highest score is 192. The GCQ was adapted for use in a Turkish context by Kuğuoğlu and Karabacak.
immediately after cystoscopy procedure is completed

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hanife Durgun, Dr, Ordu State 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)

April 1, 2019

Primary Completion (ACTUAL)

January 31, 2020

Study Completion (ACTUAL)

January 31, 2020

Study Registration Dates

First Submitted

May 18, 2020

First Submitted That Met QC Criteria

June 1, 2020

First Posted (ACTUAL)

June 2, 2020

Study Record Updates

Last Update Posted (ACTUAL)

June 2, 2020

Last Update Submitted That Met QC Criteria

June 1, 2020

Last Verified

June 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HanifeD

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.

Clinical Trials on Cystoscopy

Clinical Trials on music therapy

3
Subscribe