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The Effect of Creating a Birth Story in the Labor Room on Fear of Childbirth

I

Inonu University

Status

Completed

Conditions

Birth

Treatments

Behavioral: BIRTH STORY EXPERIMENTAL GROUP

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to reduce the fears of women who will give birth and increase their comfort. In the literature review conducted for this purpose, no study has yet been found that examines the effect of creating a birth story in the labor room on the fear of birth and birth comfort in primiparous pregnant women. In order to fill this gap in the literature, pregnant women in the labor room will be asked to create their birth stories and the effect of this on fear of birth and birth comfort will be examined.

The hypotheses of the study are as follows:

H1a: Creating a birth story in the labor room affects fear of birth H1b: Creating a birth story in the labor room affects birth comfort.

Full description

The aim of this study is to examine the effect of creating a birth story in the labor room on the fear of childbirth and the comfort of pregnant women. Data will be collected from primiparous pregnant women who are admitted to the labor room in the maternity ward of Gölbaşı State Hospital and are in the latent phase. Women will be informed about the study and will be asked whether they will participate in the study. Informed consent forms will be distributed to women who agree to participate in the study. Data collection tools will be applied to women who agree to participate in the study by the researcher through face-to-face interviews. Data collection will be completed with the end of the latent phase (≥ 4-6 cm). No intervention will be applied to women in the control group, however, the Personal Information Form, Prenatal Self-Assessment Scale-Fear of Childbirth Subscale and Childbirth Comfort Scale will be applied simultaneously with the experimental group. Pre-test data collection questionnaires will be applied to pregnant women in the experimental group at the beginning of the latent phase and pregnant women will be asked to create their own birth stories. A transparent wall board will be attached to the wall of the labor room and pregnant women will be given appropriate pens and asked to write their feelings and thoughts on this board and in this way, birth stories will be created. If pregnant women wish, their photographs will be taken and attached to this board. After the birth story is created, the post-test data collection tools will be applied to the pregnant woman again and the data collection process will be completed.

Enrollment

58 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:- All primiparous pregnant women who are literate,

  • Over the age of 18,
  • Not experiencing a risky pregnancy,
  • Not becoming pregnant with assisted reproductive techniques,
  • Planned to have a vaginal birth,
  • In the latent phase of labor,
  • Do not have any psychiatric disorders,
  • Do not have any health problems in themselves or their babies,
  • Do not have a history of ex fetus will be included in the study.

Exclusion Criteria:

  • Pregnant women with an indication for caesarean section during the latent phase of labour will not be included in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

58 participants in 2 patient groups

No Intervention:
No Intervention group
Description:
GROUP WITHOUT BIRTH STORY
Experimental
Experimental group
Description:
Birth story creating group
Treatment:
Behavioral: BIRTH STORY EXPERIMENTAL GROUP

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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