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Clinical Trials/NCT06290700
NCT06290700CompletedNot Applicable

Effect of Neonatal Care Education for Primiparous Pregnant Women on Postpartum Maternal Function and Quality of Life: Randomised Controlled Trial

Celal Bayar University1 site in 1 country126 target enrollmentStarted: November 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
126
Locations
1
Primary Endpoint
severity of maternal function by Barkin Index of Maternal Functioning

Study Overview

Brief Summary

This study aimed to evaluate the effect of neonatal care education for primiparous pregnant women on postpartum maternal function and quality of life.

Detailed Description

This was a single blind randomised controlled experimental study. The sample size of the study was calculated using the G*Power 3.1.7 program, considering a 5% margin of error and 95% confidence interval, and was determined to be at least 61. Therefore, the sample was planned to consist of 122 pregnant women, including 61 pregnant women in the intervention group and 61 pregnant women in the control group.

Study Inclusion Criteria Being at least a primary school graduate. Being a primiparous pregnant woman. Being able to provide feedback. Study Exclusion Criteria Being a multiparous pregnant woman. Being a high-risk pregnant woman. Participants who met the study inclusion criteria were provided with information about the purpose and conduct of the study, and their consent to participate was then obtained. The interviews were conducted in the breastfeeding room at the Uşak Dikilitaş Family Health Centre. The data were collected between November 2022 and November 2023. The Family Health Centre has two vaccination rooms, two antenatal care rooms, two observation rooms, and two breastfeeding rooms. Each pregnant woman was individually enrolled in an education session held in the breastfeeding room. The breastfeeding room was approximately 20 m², which was considered standard for accommodating training for an average of three pregnant women. The breastfeeding room was quiet, had a suitable temperature, and was located on the first floor in the middle of the corridor.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Being at least a primary school graduate.
  • Being a primiparous pregnant woman.
  • Being able to provide feedback.

Exclusion Criteria

  • Being a multiparous pregnant woman.
  • Being a high-risk pregnant woman.

Arms & Interventions

Control group

No Intervention

All pregnant women, those in the control group, were provide with standard

İntervational group

Experimental

Neonatal care education given to primiparous pregnant women affect their postpartum maternal function Neonatal care education given to primiparous pregnant women affect their postpartum quality of life?

Intervention: Neonatal Care education (Behavioral)

Outcomes

Primary Outcomes

severity of maternal function by Barkin Index of Maternal Functioning

Time Frame: 10 weeks after after the intervention

The scale was used 6 weeks after childbirth

Secondary Outcomes

  • Maternal Postpartum Quality of Life Instrument(10 weeks after after the intervention)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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