The Effect of Potcost Stories on Childbirth Fear,

December 14, 2024 updated by: Mine Gokduman Keles, Burdur Mehmet Akif Ersoy University

The Effect of Potcost Stories on Childbirth Fear, Pain and Delivery Method

Birth is an important period that affects a woman's life physically, psychologically and socially. Although this experience can bring joy, it can also be accompanied by anxiety and fear. Fear of birth is affected by people's past traumatic birth experiences, lack of information, and the transfer of birth experiences experienced by individuals . Birth stories are one of the most accessible and frequently used tools for women to learn about birth. These stories are seen to affect women's fears of birth and their birth preferences .This study will evaluate the impact of Potcost Stories on childbirth-related fear, pain, experiences and mode of delivery.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Birth is an important period that affects a woman's life physically, psychologically and socially. Although this experience can bring joy, it can also be accompanied by anxiety and fear. Fear of birth is affected by people's past traumatic birth experiences, lack of information, and the transfer of birth experiences experienced by individuals . Birth stories are one of the most accessible and frequently used tools for women to learn about birth. These stories are seen to affect women's fears of birth and their birth preferences .The World Health Organization (WHO) has emphasized the importance of education given during pregnancy in reducing a positive birth experience and fear of birth. . Advances in technology have made podcasts, videos, and mobile phone applications (apps) widely used in training. As a result of these trainings, behavioral changes are observed in people. It has been reported that being supported by midwives during pregnancy and encouraging birth as a positive experience reduces the fear of birth . Therefore, sharing positive birth stories in pregnancy schools and antenatal care is of great importance. However, it is thought that using podcast stories and sharing women's positive birth experiences together will reduce fear during birth and increase vaginal birth. Therefore, in this study, a podcast of stories that pregnant women can listen to again whenever they want, including positive birth experiences, was prepared. This study aimed to determine the effects of potcost stories on fear, pain, satisfaction and birth outcomes related to birth. We aim for the findings and results of the study to contribute to the midwifery and nursing care literature.

This study will evaluate the effects of Potcost Stories on fear, pain, experiences and delivery type related to birth.

Study Type

Interventional

Enrollment (Estimated)

96

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

Those who have completed at least primary school education

  • Those who can speak, understand and write Turkish
  • Those between the ages of 18-35
  • Those who have spontaneous pregnancy
  • Those who volunteer to participate in the study
  • Those who are in the 24th week of pregnancy according to their last menstrual period (LMT) or ultrasound (USG) records
  • Those who have no risk factors
  • Those who have a phone number that can be used for educational interviews
  • Those who attend a pregnancy school

Exclusion Criteria:

  • Those who have fear of childbirth

    • Those who have chronic and/or psychiatric health problems
    • Those who did not attend at least three sessions of the education program
    • Those who were at risk during the pregnancy at any stage of the study
    • Those who could not be interviewed within the first 24 hours after birth were excluded from the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Group
Active Comparator: Potcost Stories

ositive birth stories were listened to by women who gave birth in the hospital included in the study and created with their permission. The podcast recording was done in a single session. These positive birth stories were expertly reviewed by 3 obstetricians and 3 academics. Each podcast content is 10 to 20 minutes (Cai et al., 2023). A WhatsApp reminder msg will be sent so that the stories are not forgotten.

In addition, the pregnant woman will be contacted by phone and trained to listen (Cai et al., 2023).

Participants will be allowed to listen to the podcasts as much as they want (Cai et al., 2023). After listening to each story, their feedback will be received and the participants' doubts will be clarified. (Cai et al., 2023; Çankaya and Şimşek, 2021; Mousavi et al., 2022).

Based on multimedia principles, podcast positive birth experiences will be prepared (Clark and Mayer, 2023). Week 24, Week 30-32, Week 36-38 First story

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Wijma Birth Expectation/Experience Scale (W-DEQ) Version A
Time Frame: 1 MOUNT

The Wijma Birth Expectation/Experience Scale Version A (W-DEQ A), developed by K. Wijma et al. in Sweden in 1998, was adapted to Turkish by Körükçü et al. in 2012. The W-DEQ consists of 33 items and is a six-point Likert-type scale.

The item responses are numbered from 0 to 5, with 0 indicating "completely" and 5 indicating "not at all". The minimum score that can be obtained from the scale is 0, and the maximum score is 165.

The cut-off value is 85 points, and a score of 85 and above is expressed as clinical fear. A high total scale score means that the degree of fear experienced is also high.

  • W-DEQ score ? 37 is mild,
  • W-DEQ score = 38-65 is moderate,
  • W-DEQ score = 66-84 is severe,
  • W-DEQ score ? 85 indicates clinical fear. Questions 2, 3, 6, 7, 8, 11, 12, 15, 19, 20, 24, 25, 27 and 31 in the scale are negatively loaded and are calculated by reversing in order to ensure compliance in the measurement. The Cronbach a
1 MOUNT
VASA Pain
Time Frame: 1 HOUR
The numerical pain rating scale (NAS) is used to assess pain intensity. In the numerical rating scale, pain is rated between 0 (absence of pain) and 10 (unbearable pain) (Price et al., 1983)
1 HOUR
Birth Experience Questionnaire (CEQ)
Time Frame: 1 HOUR

The Birth Experience Questionnaire (CEQ), developed by Dencker et al. in 2010, was adapted to Turkish by Mamuk et al. in 2019. The scale, which was developed to measure women's birth experience in different dimensions, has four sub-dimensions and 22 items. It consists of the Birth process with 8 items, Professional help / Support with 5 items, Perceived Security / Memories with 6 items and Participation in Decisions with 3 items.

  • Questions 1, 2, 4, 5, 6, 19, 20, 21 in the Birth Process sub-dimension;
  • Questions 13, 14, 15, 16, 17 in the Professional help / Support sub-dimension;
  • Questions 3, 7, 8, 9, 18, 22 in the Perceived Security / Memories sub-dimension;
  • Questions 10, 11, 12 are included in the Participation in Decisions sub-dimension.

The first 19 items of the scale are in the four-point Likert type and are scored from 1 to 4.

• Completely agree = 1, • Mostly agree = 2, • Partially agree = 3, • Strongly disagree = 4.

The last three

1 HOUR

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

January 1, 2025

Primary Completion (Estimated)

July 30, 2025

Study Completion (Estimated)

August 30, 2025

Study Registration Dates

First Submitted

December 9, 2024

First Submitted That Met QC Criteria

December 14, 2024

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 14, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2024/11 GO 2024/596

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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