The Effect of Education Given to Parents of Children With Ventriculoperitoneal Shunt on Their Anxiety and Self-efficacy

Last updated: March 14, 2024
Sponsor: Pamukkale University
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

online education

Clinical Study ID

NCT06313879
PamukkaleU-SBE-SA-01
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

This study aims to evaluate the effect of tele-education given to parents of children with ventriculoperitoneal shunt on their anxiety and self-efficacy.

Eligibility Criteria

Inclusion

Inclusion Criteria:

    1. Having a child aged 0-6 with a ventriculoperitoneal shunt 2. Volunteering toparticipate in the research

Exclusion

Exclusion Criteria:

    1. Having difficulty accessing the Internet 2. Not joining the online group 3. Notanswering survey questions 4. Having a child over 6 years of age withventriculoperitoneal shunt

Study Design

Total Participants: 60
Treatment Group(s): 1
Primary Treatment: online education
Phase:
Study Start date:
March 10, 2024
Estimated Completion Date:
February 28, 2025

Study Description

This study aims to evaluate the effect of tele-education given to parents of children with ventriculoperitoneal shunt on their anxiety and self-efficacy. The type of research was planned as a prospective, randomized controlled experimental study with a pretest-posttest control group. The research will be conducted online with the parents of children with ventriküloperitoneal shunts at Pamukkale University Hospital. The data of the research will be collected between March 2024 and February 2025. In data collection, a personal information form will be used to determine the socio-demographic characteristics of the participants, a parent knowledge test will be used to evaluate their knowledge levels, and the General Self-Efficacy Scale and State and Trait Anxiety Scale will be used to evaluate the dependent variables. It was determined that 60 parents should participate in the study, 30 for the experimental group and 30 for the control group. As the randomization method, "simple randomization" will be used to ensure an equal number of samples in the experimental and control groups. Randomization will be done using the www.randomizer.org application. The data will be analyzed with the SPSS (23.0) package program. Continuous variables will be given as mean ± standard deviation and categorical variables will be given as number and percentage. Significance Test of Difference Between Two Means in comparing independent group differences when parametric test assumptions are met; When parametric test assumptions are not met, Mann-Whitney U test will be used to compare independent group differences.

Connect with a study center

  • Pamukkale University Hospital

    Denizli, 20180
    Turkey

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.