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Effect of Cough Trick Method and Pinwheel Blowing in Blood Collection

NCT06230601 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2024-07-11

No results posted yet for this study

Summary

This study aimed to examine the effect of the cough trick method and pinwheel blowing on the severity of pain during blood collection in school-age children.The study will be conducted with children aged 6-12 years who are subjected to blood tests by a pediatrician."Descriptive Questionnaire", "Visual Analogue Scale (VAS)", "FLACC Pain Rating Scale" and "Wong-Baker Faces Pain Rating Scale (WBFPRS)" will be used to collect data.The data will be uploaded to the computer and coded by the researchers, and the data will be evaluated in the SPSS package program.The sociodemographic data of the children participating in the study will be given as numbers and percentage distributions. Appropriate tests will be used by analyzing the data for normal distribution. The statistical significance level of the study was determined as p\< 0.05. In addition, at the end of the research, the status of working with sufficient sample size will be tested with post-hoc power analysis.

Conditions

  • Child Development
  • Nursing Care
  • Pain

Interventions

OTHER

Cough Trick Method

During the Blood Collection Procedure in School-Age Children, one group will use the Cough Trick Method

OTHER

Pinwheel Blowing method

Pinwheel Blowing method

Sponsors & Collaborators

  • Firat University

    lead OTHER

Principal Investigators

  • Zeynep KİSECİK ŞENGÜL · Kirikkale Universty

  • Rüveyda OĞUZ · Firat University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-02-10
Primary Completion
2024-03-15
Completion
2024-03-15

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06230601 on ClinicalTrials.gov