The Effect of Using Finger Puppets and Showing Cartoons on Pain and Fear in Preschool Children During Blood Collection

November 19, 2025 updated by: Zeynep Camkıran, Hitit University

The Effect of Using Finger Puppets and Showing Cartoons on Pain and Fear in Preschool Children (3-6 Years Old) During Blood Collection

The study is a randomized controlled experimental study aimed at determining the effect of showing cartoons or using finger puppets to children aged 3-6 years before taking venous blood samples on their pain levels.

Based on the results of this study, it is thought that showing cartoons and using finger puppets before blood collection will help reduce pain levels in children and improve their ability to cope with pain, thereby improving the quality of care. In this context, the study will be conducted to determine the effect of showing cartoons and using finger puppets before blood collection on pain in pediatric patients.

Study Overview

Detailed Description

Children between the ages of three and six have the language skills to express pain at a sensory level. They can describe the location and intensity of the pain. They may cry, scream, and exhibit aggressive behavior in response to pain. They may think of invasive procedures such as blood collection as punishment. Before any procedures are performed, the child should be informed about the procedures that will be performed and their stress and fear should be reduced by helping them relax. Nurses should use non-pharmacological methods appropriate for the age group of the children during painful procedures to reduce the level of pain perceived by the children. In this study, I will examine the effect of showing cartoons and finger puppets to children during blood collection on pain and fear.

Study Type

Interventional

Enrollment (Actual)

120

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

    • Merkez
      • Çorum, Merkez, Turkey (Türkiye), 19200
        • Hitit University Erol Olçok Education 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

  • Child

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • The child and parent agree to participate in the study.
  • The child is between 3 and 6 years old.
  • The child has no acute pain complaints.
  • The child has no disabilities.

Exclusion Criteria:

  • The child and parent refuse to participate in the study.
  • The child is under 3 years of age or over 6 years of age.
  • The child has acute pain complaints.
  • The child has any disability.

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: finger puppet group
During the blood collection procedure, 40 children were randomly selected to play with finger puppets.
finger puppets
Experimental: watching cartoons group
During the blood collection procedure, 40 children were randomly selected to watch cartoons.
Watching cartoons during blood collection
Experimental: control group
No intervention was performed on the children.
No intervention was made during blood collection

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Wong-Baker Faces Pain Rating Scale
Time Frame: 4 months

Pain scores are given according to the numerical values assigned to the faces on this scale. It is explained to the child that the faces on the scale do not represent people who are happy because they are not in pain or unhappy because they are in pain.

A very happy person is Face 0. A little pain is Face 1, a little more pain is Face 2, a little more pain is Face 3, and quite a lot of pain is Face 4. Face 5 represents the highest level of pain that can be imagined. The child is asked to choose the face that best describes the pain they are feeling.

4 months
Children's Fear Scale (CFS)
Time Frame: 4 months

CFS is used to score the fear that may cause pain in children before or during the procedure. The scale is a visual measurement tool consisting of five drawn lines ranging from a neutral facial expression (0 = no fear) to a frightened facial expression (4 = very afraid), with scores ranging from 0 to 4.

The scale is used to assess the fear of pain in children before or during a procedure.

The scale is a visual measurement tool consisting of five drawn lines ranging from a neutral facial expression (0 = no fear) to a frightened facial expression (4 = very afraid), with scores ranging from 0 to 4.

The scale is used to assess the fear of pain in children before or during a procedure. . The Turkish language validity and psychometric properties of the scale used to assess procedural fears in children aged 5-12 were tested

4 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Information Form
Time Frame: 4 months
Information Form: The form includes questions regarding the date of the procedure, the reason for the children's admission to the hospital, the duration of the procedure, the method used, the children's age, gender, whether they had received analgesics in the last 24 hours, whether they had undergone a blood draw in the last 6 months, whether any preparatory measures were taken before the blood draw and, if so, which method was used, the parents' age, family structure, and family education level.
4 months

Collaborators and Investigators

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

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)

May 10, 2025

Primary Completion (Actual)

July 25, 2025

Study Completion (Estimated)

December 1, 2025

Study Registration Dates

First Submitted

October 1, 2025

First Submitted That Met QC Criteria

November 17, 2025

First Posted (Estimated)

November 19, 2025

Study Record Updates

Last Update Posted (Actual)

November 26, 2025

Last Update Submitted That Met QC Criteria

November 19, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

I will not share the work data with anyone.

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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