ClinicalTrials.gg
RecruitingNCT05964426Updated Jul 23, 2024

Health Literacy of Parents Regarding Neonatal Jaundice

An observational study in Unspecified Fetal and Neonatal Jaundice, sponsored by Ege University. Recruiting at 1 site in Turkey. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-07-23.

Sponsored by Ege University · Observational

From the registry’s dates

  • Started Jul 2024; still recruiting 2 years 4 months later.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
170
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 17 studies in Jaundice, Neonatal with a site in Turkey — 3 open to participants now, 4 under way, none of them phase 3. Jaundice, Neonatal · Turkey.

Started
2024
with 1 other
Observational
4 of 17
2 open now
Registered
8th of 17
by date
Lead sponsor
2 of 17
Ege University

Among the 17 studies in Jaundice, Neonatal with a site in Turkey, this one is one of 2 that started in 2024, is one of 4 observational ones, and was the 8th registered.

Jaundice, Neonatal

110 studies on the registry are indexed under Jaundice, Neonatal; 28 are open to participants now.

Browse Jaundice, Neonatal studies →

Open to participants now

3 of the 17 studies in Jaundice, Neonatal with a site in Turkey are open now. Recruiting first, the newest first:

All 3 open studies →

A study can be open while its sites in Turkey have not opened yet or have stopped. Only those recruiting at a site in Turkey →

Who these studies take

Of the 13 Jaundice, Neonatal studies recruiting now, 1 (8%) sets no upper age limit and 12 (92%) stop at 75 or younger; 11 take children under 18; 8 take healthy volunteers.

This study: 18 Years and older · all sexes · healthy volunteers too.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 17 studies in Jaundice, Neonatal with a site in Turkey, or all of them as a file.
02

Study summary

This study will be conducted as a relational descriptive study to determine the health literacy level of parents with infants between 0-28 days of age regarding neonatal jaundice. The secondary aim of the study is to examine whether the health literacy levels of the parents differ with parent and infant descriptive characteristics and their knowledge about neonatal jaundice. In this study, answers to the following questions were sought.

  1. What is the level of knowledge about neonatal jaundice among parents with infants between 0-28 days?
  2. What is the level of health literacy of parents with infants between 0-28 days of age and is there a relationship between parent, infant identifying characteristics and knowledge about neonatal jaundice?
Read the detailed description

Objective: This study will be conducted as a relational descriptive study to determine the health literacy level of parents with infants between 0-28 days of age regarding neonatal jaundice. The secondary aim of the study is to examine whether the health literacy levels of the parents differ with parent and infant descriptive characteristics and their knowledge about neonatal jaundice.

Methodology of the research: The research is a descriptive study in relational design. It is a study design in which the relationships between two or more variables are examined, aiming to examine whether one variable causes any change in the other variable.

Population of the Study: Parents with newborn babies aged between 0-28 days who live in Turkey and can be reached.

While determining the sample of the study; using G-Power 3.1.9.7 program; type 1 error (α) 0.05, power (1- β) 80% and Cohen's effect size (δ) 0.2, the sample size to represent the main mass was determined as 156 people for this study. However, when the dropout rate is set as 10% for data loss that may occur in the study, the minimum number to be reached for the study is targeted as 170 people.

Snowball processing method, one of the simple processing methods, will be used to reach the sample size. In this method, a reference person related to the subject of the study is selected and other people are reached through this person.For snowball sampling, we will primarily contact pregnant women over 28 weeks of gestation and mothers with newborns in our area via social media, WhatsApp or e-mail. Then, the sample will be reached in the form of pregnant women and mothers who are known to these pregnant women and mothers. Since the researcher is located in the Central Anatolia Region, the sample density is expected to be from the Central Anatolia region. Surveys will be created with an online survey (Google Form) and sent to pregnant women and mothers via social media, WhatsApp or e-mail.

Independent Variables: The independent variables of the study included age, education level, family type, place of residence, whether the parents had other children, how many days old the baby was, gender of the baby, blood type of the mother, father and baby, whether the baby was given formula in addition, whether the parents had sufficient information about neonatal jaundice, from whom they received the information, what their reaction would be if their baby got jaundice, information about the causes, symptoms and complications of jaundice.

Dependent Variables: The mean score of the health literacy scale of the parents constituted the dependent variables.

The research data will be collected through the 'Introductory Information Form on Mother and Infant', 'Parent Information Form on Neonatal Jaundice' and 'Turkey Health Literacy Scale' which were created by the researcher using the literature.

Data Analysis: Statistical Package for Social Sciences 25.0 package program will be used to analyze the data. Descriptive characteristics of the parents will be given as frequency (f), percentage (%) and mean. Normality distribution will be determined by Shapiro-Wilk test. In the analysis of normally distributed data; t-test will be used to determine whether there is a difference between two independent groups, and one-way ANOVA will be used to determine whether there is a difference between more than two independent groups. In the analysis of non-normally distributed data, Mann Whitney-U will be used to determine whether there is a difference between two independent groups and one-way Kruskal-Wallis will be used to determine whether there is a difference between more than two independent groups. The findings obtained will be evaluated at 95% confidence interval and significance at p\<0.05 level.

03

Conditions studied

  • Unspecified Fetal and Neonatal Jaundice

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Keywords

  • Health literacy
  • neonatal jaundice
  • newborn
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

It will be carried out with parents who have a newborn between 0-28 days who applied to Beyşehir State Hospital, Pediatrics Polyclinics.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Theparent has a baby aged 0-28 days, The parent does not have any speech-vision-hearing disability that would prevent communication,
  • The parent speaks Turkish,
  • Parental literacy
  • It was determined by taking into consideration the criteria of volunteering to participate in the research.

Exclusion criteria

Exclusion Criteria:

-Parents who do not meet the inclusion criteria will be excluded.

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
170 participants (estimated)
Patient registry
No

Groups and cohorts

  • Parent and Infant Information Form

    This form consists of a total of 19 questions in line with the literature, including the parents' age, education level, family type, place of residence, whether they have other children, how many days their baby is, gender of the baby, maternal blood type, paternal blood type, and whether the baby is given formula in addition.

    Other: Turkey Health Literacy Scale (TSOY-32)

  • Parent Information Form on Neonatal Jaundice

    This form consists of a total of 6 questions in line with the literature, including whether the parent has sufficient information about neonatal jaundice, from whom he/she received the information, what his/her reaction will be if his/her baby gets jaundice, and information about the causes, symptoms and side effects of jaundice.

    Other: Turkey Health Literacy Scale (TSOY-32)

  • Turkey Health Literacy Scale (TSOY-32)

    It is a 32-question scale developed based on the Conceptual Framework of the European Health Literacy Scale Study. The Turkish Health Literacy Scale (TSOY-32) was developed to assess health literacy in literate people over the age of fifteen. Unlike the original scale, the scale consists of eight components including two dimensions (treatment and service, disease prevention and health promotion) and four processes (accessing health-related information, understanding health-related information, evaluating health-related information, and using/applying health-related information). The overall internal consistency coefficient of the scale was 0.92. The Cronbach's alpha coefficient of the first dimension 'Treatment and Service Subdimension' is 0.88. The Cronbach's alpha coefficient of the second dimension 'Disease Prevention and Health Promotion Dimension' is 0.86. Permission to use the scale was obtained.

    Other: Turkey Health Literacy Scale (TSOY-32)

Interventions

  • OtherTurkey Health Literacy Scale (TSOY-32)

    A survey will be conducted.

    Also known as: Parent and Infant Information Form, Parent Information Form on Neonatal Jaundice

06

What researchers measure

Primary outcomes

  1. It is planned as a relational descriptive study to determine the level of health literacy of parents with babies between 0-28 days of age regarding neonatal jaundice.

    To determine the health literacy levels of parents with 0-28 days old babies regarding neonatal jaundice. Accordingly, the scores of the Turkish Health Literacy Scale (TSOY-32) are given below. * (0-25) points: insufficient health literacy * (\>25-33) score: problematic - limited health literacy * (\>33-42) score: adequate health literacy * (\>42-50) score: excellent health literacy

    Time frame: August 1 2024 - December 31 2024

Secondary outcomes

  1. The secondary aim of the study was to examine whether parents' health literacy levels differed with parent and infant descriptive characteristics and knowledge about neonatal jaundice.

    The secondary aim of the study is to examine whether the health literacy levels of the parents \[Turkish Health Literacy Scale (TSOY-32)\] differ according to their parental and infant descriptive characteristics and their knowledge about neonatal jaundice (significance p\<0.05).

    Time frame: August 1 2024- December 31 2024

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jul 2024 to primary completion in Jul 2024, 0 months.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 22, 2023
First posted
Jul 28, 2023
StartActual
Jul 1, 2024
Primary completionActual
Jul 20, 2024
CompletionEst.
Dec 31, 2024
Last update
Jul 23, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 23, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05964426
Lead sponsor
Ege University
Collaborators
Associate Professor Figen YARDIMCI
Responsible party
Tuba GIYNAS (clinical nurse, Ege University) — Principal investigator
First posted
Jul 28, 2023
Start date
Jul 1, 2024
Primary completion
Jul 20, 2024
Completion
Dec 31, 2024 (estimated)
Last update
Jul 23, 2024

Study contacts

Figen YARDIMCI
Contact
figenyardimci@gmail.com
05388806835

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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