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The Effect of Web-based Training Given to Mothers of Babies With Congenital Heart Disease

Not Applicable
Completed
Conditions
Quality of Life
Training
Self Efficacy
Mothers
Registration Number
NCT06168344
Lead Sponsor
Saglik Bilimleri Universitesi
Brief Summary

This study was assessed the impact of a web-based education program provided to mothers of infants with congenital heart diseases on their quality of life and self-efficacy levels. The study is a mixed-method approach with a qualitative and pre-test post-test design, utilizing randomized controlled quasiexperimental type.

The research was conducted with mothers of infants diagnosed with congenital heart disease who sought care at the Pediatric Cardiology Outpatient Clinic of a university hospital and were followed up. There are two groups in the study. Web-based education was provided to mothers in the intervention group (n=30). No intervention was applied to the mothers in the control group (n=30) other than the outpatient clinic routine of the hospital.

Detailed Description

Materials and Methods: study is a mixed-method approach with a qualitative and pre-test post-test design, utilizing randomized controlled quasiexperimental type. The research was conducted with mothers of infants diagnosed with congenital heart disease who sought care at the Pediatric Cardiology Outpatient Clinic of a university hospital and were followed up. There are two groups in the study. Web-based education was provided to mothers in the intervention group (n=30). No intervention was applied to the mothers in the control group (n=30) other than the outpatient clinic routine of the hospital. "Qualitative interview form, Parent-infant Introductory Information Form, Quality of Life Scale and Generalized Perceived Self-Efficacy Scale" were used. The research process had two stages; in the first stage, qualitative data was collected and after qualitative interviews with mothers, the content of the web-based training was created in line with the needs of the mothers. In the second stage, quantitative data were collected, and a web-based training program was applied to the intervention group and an outpatient clinic routine to the control group.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • For mothers;
  • Having a baby with congenital heart disease
  • Being over 18 years of age
  • Being literate
  • Being able to speak and understand Turkish
  • There is no health problem that may prevent participation in training.
  • Being able to use a computer/mobile phone
  • Being able to use and have internet access
  • Volunteering to participate in research

For babies;

  • Those born at or after the 37th week of gestation and those with congenital heart disease, aged 0-12 months
  • Has not had heart surgery
  • Babies who do not have any other chronic diseases
Exclusion Criteria
  • Filling out forms incompletely
  • Being a foreign national
  • Having vision or hearing problems
  • To give up participating in the research
  • Mothers and babies who have physical/mental problems that may affect the research results during the study period.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Qualitative Interview FormIn the first stage of the research; Qualitative data were collected: once

In the first stage of the research; Qualitative data were collected. Qualitative interviews were conducted with mothers (n=11). Seven open-ended questions were asked. Categories and themes were arranged according to the content analysis created from the data. The content of the Web-based training program was created in line with the needs and requirements of mothers according to categories and themes.

Secondary Outcome Measures
NameTimeMethod
Parent-Baby Identification Information FormForm was administered to mothers in both groups before the study: once.

The form consists of a total of 23 questions and two sections. The first part consists of 14 questions to evaluate the socio-demographic characteristics of parents. Second part consists of nine questions to evaluate the demographic characteristics of babies.

Trial Locations

Locations (1)

Eskişehir Osmangazi University Health Practice and Research Hospital

🇹🇷

Eskişehir, Turkey

Eskişehir Osmangazi University Health Practice and Research Hospital
🇹🇷Eskişehir, Turkey

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