Viewing Study NCT04897906



Ignite Creation Date: 2024-05-06 @ 4:10 PM
Last Modification Date: 2024-10-26 @ 2:05 PM
Study NCT ID: NCT04897906
Status: COMPLETED
Last Update Posted: 2023-01-13
First Post: 2021-05-18

Brief Title: The Effect of Education Given to Primiparous Pregnant Women on Parental Self-Efficacy and Mother-Infant Attachment
Sponsor: University of Beykent
Organization: University of Beykent

Study Overview

Official Title: The Effect of Education Given to Primiparous Pregnant Women on Parental Self-Efficacy and Mother-Infant Attachment
Status: COMPLETED
Status Verified Date: 2023-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This research will be carried out in a quasi-experimental design to determine the effect of maternity care and neonatal care training given to primiparous pregnant women on parental self-efficacy and mother-infant attachment in the postpartum period

Research Hypotheses

H0 There is no difference in parental self-efficacy and mother-infant attachment in the postpartum period between pregnant women who received training during pregnancy and did not

H1 There is a difference in parental self-efficacy and mother-infant attachment in the postpartum period between pregnant women who received and did not receive education during pregnancy
Detailed Description: The number of people to be included in the study was made with the power analysis made considering the previous studies With the G Power 3197 Program the number of samples for each group was determined as n 34 at 80 power 5 error and 95 confidence interval Considering the losses in data collection 20 was added to each group and it was decided to recruit a total of 80 people 40 people for the experimental group and 40 people for the control group

Pregnant women included in the research sample will be divided into two groups as experimental and control groups Data will be collected by sending via an online questionnaire created by the researchers Before the online questionnaire is sent to the experimental and control groups the experimental-control days will be determined randomly by a lottery drawn by a third person blinding Pregnant women who agree to participate in the study will be assigned to the experimental and control groups according to the determined days

The data obtained in the study will be analyzed using the SPSS Statistical Package for Social Sciences for Windows 220 program Significance value will be considered as p 005

Number percentage mean and standard deviation will be used as descriptive statistical methods in the evaluation of data Pearson correlation and regression analysis will be applied among the continuous variables of the study The t-test will be used to compare the quantitative continuous data between two independent groups and the One-way Anova test will be used to compare the quantitative continuous data between more than two independent groups After the Anova test the Scheffe test will be used as a complementary post-hoc analysis to determine the differences

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None