Training Given in the Line of Coping With Fear of Birth on Fear of Birth Birth Experience

Sponsor

Cukurova University (Other)

Overall Status

Recruiting

CT.gov ID

NCT05928117

Collaborator

(none)

Enrollment

Location

Arms

Anticipated Duration (Months)

5.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Pregnancy and childbirth are a natural life event for women, as well as a process in which physical, biological and psychosocial changes are experienced. This process causes women to perceive childbirth as an unknown and unpredictable situation, resulting in the fear of childbirth. Due to the fear of childbirth, the daily routines, professional lives, social activities and relationships of pregnant women are significantly affected.

This study was planned to evaluate the effect of mobile education given in line with the "Guide to Coping with Fear of Birth" on fear of birth, birth preference and maternal satisfaction at birth. Research; It will be carried out at the T. C. Ministry of Health Gaziantep Cengiz Gökçek Gynecology and Pediatrics Hospital. Data; The first one is 28-30th of pregnancy. week, the second is 36-38. It will meet in three meetings in total, the third of which will be within 12-24 hours postpartum. Data, Personal Information Form (Annex-1), Wijma Birth Expectation/Experience Scale (W-DEQ) Version A (Annex-2), Wijma Birth Expectation/Experience Scale Version B (Annex-3) and Birth Experience Scale ( Annex-4) and Postpartum Questionnaire (Annex-5). The obtained data will be analyzed with the SPSS 22.0 program.

In this study, it is thought that the training given to women with a high level of birth fear can reduce their fear of childbirth and increase maternal satisfaction at birth.

Condition or Disease	Intervention/Treatment	Phase
Birth Fear of Childbirth Education Pregnancy Fear	Other: Education	N/A

Detailed Description

The study is a randomized controlled management type study conducted to determine the effect of individual mobile training, which is reached by the "Guidelines for Coping with Fear of Birth" for primitive pregnant women.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

67 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

Experimental and control groupsExperimental and control groups

Masking:

Single (Participant)

Primary Purpose:

Supportive Care

Official Title:

The Effect of Mobile Training Given in the Line of Coping With Fear of Birth on Fear of Birth, Birth Preference and Birth Experience

Actual Study Start Date :

Aug 1, 2022

Anticipated Primary Completion Date :

Aug 1, 2023

Anticipated Study Completion Date :

Sep 1, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Experimental Intervention: Mobile education given in the line of coping with fear The first one is 28-30th of pregnancy. week, the second is 36-38. It will meet in three meetings in total, the third of which will be within 12-24 hours postpartum.	Other: Education Pregnant women will be given training to cope with the fear of childbirth. Other Names: Training to cope with the fear of childbirth education
No Intervention: Control Standart care

Arm

Intervention/Treatment

Experimental: Experimental

Intervention: Mobile education given in the line of coping with fear The first one is 28-30th of pregnancy. week, the second is 36-38. It will meet in three meetings in total, the third of which will be within 12-24 hours postpartum.

Other: Education

Pregnant women will be given training to cope with the fear of childbirth.

Other Names:

Training to cope with the fear of childbirth education

No Intervention: Control

Standart care

Outcome Measures

Primary Outcome Measures

Fear of birth [Pre-test: Wijma Birth Fear/Experience version A and B were applied between 28-30 weeks of pregnancy. Post-test: Wijma Birth Fear/Experience version A and B were applied between 36-38 weeks.]
As the scale score increases, the fear of birth increases
Birth experience [Birth experience scale was applied between 12-24 hour]
As the score obtained from the scale increases, the mother has a good birth experience.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 35 Years

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

Primiparous,
Having a single fetus,
Able to read and write,
Between the ages of 18-35,
Volunteer to participate in the research,
28-30 days of pregnancy according to the last menstrual period or ultrasonography records. in the week,
No risk factors (heart disease, placenta previa, oligohydramnios, preeclampsia, anhydramnios, diabetes, epilepsy),
Having a telephone that can be contacted for mobile calls,
Pregnant women who do not have any disability diagnosed for normal delivery.

Exclusion Criteria:

Having communication problems,
Having mental deficiency,
Those who received infertility treatment and became pregnant with assisted reproductive techniques.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Cukurova University	Adana		Turkey	01330

Sponsors and Collaborators

Cukurova University

Investigators

Principal Investigator: Meltem Akbaş, PhD, Universty Of Cukurova

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Meltem Akbaş, Assistant Professor, Cukurova University

ClinicalTrials.gov Identifier:

NCT05928117

Other Study ID Numbers:

10.09.2021/49

First Posted:

Jul 3, 2023

Last Update Posted:

Jul 3, 2023

Last Verified:

Jun 1, 2023

Individual Participant Data (IPD) Sharing Statement:

Plan to Share IPD:

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Study Results

No Results Posted as of Jul 3, 2023