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Childbirth Education and Birth Plan on Birth Self Efficacy in Pregnant Women

I

Inonu University

Status

Completed

Conditions

Self Efficacy
Pregnancy Related

Treatments

Other: childbirth education
Other: childbirth education and was subjected to a birth plan

Study type

Interventional

Funder types

Other

Identifiers

NCT04525430
2017/4-3

Details and patient eligibility

About

The pregnant women constituting the sample were divided into 3 groups. Group 1 was given only childbirth education (Group-ED), group 2 was given childbirth education and was subjected to a birth plan (Group-ED&P), and group 3 was the control group, each including 51 pregnant women.

Full description

Aim: The purpose of this study was to investigate how pregnant women's childbirth self-efficacy was affected by childbirth education and birth plans applied with the education.

Methods: The research was carried out at seven Family Health Centers in Turkey as a randomized controlled trial. The pregnant women constituting the sample were divided into 3 groups. Group 1 was given only childbirth education (Group-ED), group 2 was given childbirth education and was subjected to a birth plan (Group-ED&P), and group 3 was the control group, each including 51 pregnant women.

Enrollment

153 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • pregnant women who was in the third trimester (28-40 gestational weeks),
  • who was literate or had a relative/helper who would write a birth plan to be prepared,
  • who were not involved in any diagnosed risk at the present pregnancy (such as preeclampsia, diabetes, heart disease, placenta previa, oligohydramnios and multiple pregnancy)
  • who did not have any diagnosed problems with the health of fetus (such as fetal anomaly and intrauterine growth retardation).

Exclusion criteria

• who had previous cesarean section were not included in the research.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

153 participants in 3 patient groups

Group 1
Experimental group
Description:
only childbirth education group
Treatment:
Other: childbirth education
Group 2
Experimental group
Description:
childbirth education and was subjected to a birth plan group
Treatment:
Other: childbirth education and was subjected to a birth plan
Group 3
No Intervention group
Description:
standard care group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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