Effect of Auditory Distractions on Pediatric Postoperative Pain

NCT ID: NCT03704961

Last Updated: 2018-10-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

3 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-01-31

Study Completion Date

2017-10-31

Brief Summary

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The aim of the study was to determine the effect of different auditorial methods of attention distraction on postoperative pain and anxiety in children. Three group pre and post-test randomized clinical trial.The data were collected using the Socio-demographic Data Form for Child and Parent, Visual Analogue Scale, Wong-Baker Faces Pain Scale and State-Trait Anxiety Inventory for Children. The investigators found that listening to classical music, Turkish music and audiobook methods played an effective role in decreasing postoperative pain and anxiety state in children in the three groups in the study. As a result, investigators showed that different auditorial attention distraction methods had a decreasing effect on postoperative pain and anxiety in children.

Detailed Description

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Conditions

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Pain, Postoperative

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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classical music

Group Type EXPERIMENTAL

music and audiobook listening

Intervention Type BEHAVIORAL

Turkish music

Group Type EXPERIMENTAL

music and audiobook listening

Intervention Type BEHAVIORAL

audiobook

Group Type EXPERIMENTAL

music and audiobook listening

Intervention Type BEHAVIORAL

Interventions

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music and audiobook listening

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* patients aged between 7-14 years old,
* staying in a single room,
* those for whom a surgical procedure for inguinal or abdominal region had been planned,
* in the first hour of postoperative period,
* free of any problem that prevents expression of the post-operative pain,
* free of hearing problems,
* having undergone same analgesia protocol; were included in the study.

Exclusion Criteria

\-
Minimum Eligible Age

7 Years

Maximum Eligible Age

14 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Uludag University

OTHER

Sponsor Role lead

Responsible Party

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nurcan özyazıcıoğlu

UludagU

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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1

Identifier Type: -

Identifier Source: org_study_id

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