Atraumatic Care Practice From the Child and Parent Perspective

December 14, 2023 updated by: Hatice Uzşen, Ondokuz Mayıs University
It is important for pediatric nurses to apply atraumatic care while providing care to children and their families. Pediatric nurses should use methods appropriate for the child's age and developmental period within the scope of atraumatic care.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The use of atraumatic care approaches such as supporting the active participation of the family in the care of the child, using therapeutic communication techniques with parents and children during procedures, providing emotional support, reducing pain during painful procedures, using techniques to distract the child's attention during medical procedures, informing parents about the procedures to be performed on their children, and supporting parents and teaching techniques to cope with stress is recommended to be used by the nurses.

Study Type

Interventional

Enrollment (Actual)

219

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

    • Atakum
      • Samsun, Atakum, Turkey, 55100
        • Hatice Uzşen

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • being able to speak Turkish
  • being between 5-10 years of age
  • having no visual, intellectual or neurological disabilities
  • having the phlebotomy procedure carried out with a single attempt
  • not having a disease that causes chronic pain
  • being accompanied by either mother or father during the procedure
  • not taking painkillers or sedating drugs before the phlebotomy procedure

Exclusion Criteria:

  • being younger than 5 years or older than 10 years
  • having visual, audio, or speech impairments
  • having a disease that causes chronic pain
  • with a history of sedative and analgesic use within 24 h prior to admission
  • filling out the data collection forms incompletely

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 Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Atraumatic nursing care group
Before the phlebotomy, children in the intervention group were allowed to choose a distracting method (foam balloons, stress balls, musical books) to be occupied with during the procedure. It was ensured that the parent was staying with the child and that the child played with this material during the procedure (making a foam balloon, squeezing the ball with the hand in which the procedure was not carried out and reading the book with the parent
Children in the intervention group were allowed to choose a distracting method (foam balloons, stress balls, musical books) to be occupied with during the procedure
No Intervention: Control group
The parents of the children in the control group were ensured to stay with their children during the procedure, and the child's attention was distracted by the nurse asking questions about the child's name, age, and what grade the child was in. This is one of the methods frequently used in Turkiye.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Children's Fear Scale
Time Frame: baseline, pre-intervention and immediately after the intervention
Children's Fear Scale was to measure fear in children who would undergo painful medical procedures
baseline, pre-intervention and immediately after the intervention
Wong-Baker Faces Pain Rating Scale
Time Frame: immediately after the intervention
This scale is used for 3-18 age group children to describe their pain.
immediately after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of Parental Satisfaction-Visual Analog Scale
Time Frame: immediately after the intervention
Parent satisfaction scores were collected using a question about care satisfaction during the phlebotomy procedure from each child's parent.
immediately after the intervention

Collaborators and Investigators

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

Investigators

  • Study Chair: Esra Tural Büyük, PhD, Ondokuz Mayıs 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, 2023

Primary Completion (Actual)

June 1, 2023

Study Completion (Actual)

June 30, 2023

Study Registration Dates

First Submitted

November 27, 2023

First Submitted That Met QC Criteria

December 14, 2023

First Posted (Actual)

December 15, 2023

Study Record Updates

Last Update Posted (Actual)

December 15, 2023

Last Update Submitted That Met QC Criteria

December 14, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • Atraumatic Care

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There is not a plan to make IPD available.

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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