The Effect of Education Given to Primiparous Pregnant Women on Parental Self-Efficacy and Mother-Infant Attachment

Sponsor
University of Beykent (Other)
Overall Status
Recruiting
CT.gov ID
NCT04897906
Collaborator
Istanbul University-Cerrahpasa (Other)
80
1
2
3.7
21.7

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Education Group
N/A

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 (3.1.9.7.) 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 22.0 program. Significance value will be considered as p <0.05.

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 Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Pregnant women included in the research sample will be divided into two groups as experimental and control groups. Experimental group; is the group to be trained. Control group; It is the group in which no intervention will be made other than data collection.Pregnant women included in the research sample will be divided into two groups as experimental and control groups. Experimental group; is the group to be trained. Control group; It is the group in which no intervention will be made other than data collection.
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Education Given to Primiparous Pregnant Women on Parental Self-Efficacy and Mother-Infant Attachment
Actual Study Start Date :
May 12, 2021
Anticipated Primary Completion Date :
Jul 1, 2021
Anticipated Study Completion Date :
Sep 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

Experimental group; It is the group that will be given mother and neonatal care education.

Behavioral: Education Group
Mother care, newborn care and breastfeeding education will be provided to pregnant women in the third trimester of pregnancy.

No Intervention: Control Group

Control group; It is the group in which no intervention will be made other than data collection.

Outcome Measures

Primary Outcome Measures

  1. Parental self-efficacy in postpartum period of pregnant women who received education during pregnancy [Mothers will be evaluated within 30-40 days after birth.]

    Parental Self-Efficacy Scale will be used in the evaluation. It is a scale developed to determine the personal beliefs of new parents about their competencies in their roles.

  2. Mother-Infant attachment in postpartum period of pregnant women who received education during pregnancy [Mothers will be evaluated within 30-40 days after birth.]

    Maternal Attachment Scale will be used in evaluation. It was developed to measure the mother's love and attachment to her baby. Higher scores on the scale indicate higher maternal attachment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Being at 36-40 weeks of gestation

  • Being her first pregnancy

  • Being literate

  • Being over the age of 18

Exclusion Criteria:
  • Not in the 36-40 gestational week

  • Not a first pregnancy

  • Illiterate

  • Under 18 years old

Contacts and Locations

Locations

Site City State Country Postal Code
1 Beykent University Buyukcekmece Istanbul Turkey

Sponsors and Collaborators

  • University of Beykent
  • Istanbul University-Cerrahpasa

Investigators

  • Principal Investigator: Cisem Bastarcan, MsC, Research Assistant

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cisem Bastarcan, Research Assistant, University of Beykent
ClinicalTrials.gov Identifier:
NCT04897906
Other Study ID Numbers:
  • CBastarcan
First Posted:
May 24, 2021
Last Update Posted:
May 24, 2021
Last Verified:
May 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Cisem Bastarcan, Research Assistant, University of Beykent

Study Results

No Results Posted as of May 24, 2021