The Effect of Individual Counselling Program on Fear of Childbirth

Aydin Adnan Menderes University

Status: Completed

Conditions: Pregnancy Related; Fear of Childbirth

Treatments: Behavioral: Intervention group

Study type: Interventional

Funder types: Other

Identifiers

NCT04740762

Interventional study

Details and patient eligibility

About

A randomized control trial was made to developing an individual counseling program to help women cope with their fear of childbirth and testing the program for effectiveness.

Full description

Fear of childbirth is a common problem among women and one that affects their health and welfare before and during pregnancy and in the postpartum period. The problem can lead to adverse pregnancy outcomes and also cause a woman to experience psychological issues. Fear of childbirth can also influence the determination of the mode of delivery and can amount to a rise in cesarean rates.

The healthcare provided by midwives and other healthcare professionals during pregnancy and childbirth have the power to reduce or exacerbate childbirth fears. The most significant midwifery intervention that can be used to diminish the fear of childbirth is counseling. There is a need to develop and test individual counseling models that require the basic training skills that midwives can use as part of their routine care to address women's fears and expectations about childbirth. The individual counseling program developed in this context may be an easy-to-implement and cost-effective method to use.

This study was conducted for the purposes of developing an individual counseling program to help women cope with their fear of childbirth and testing the program for effectiveness.

It was tested the hypotheses that there is no difference between the intervention and control groups of pregnant women after the intervention in terms of fear of childbirth, childbirth self-efficacy and state anxiety scores and childbirth outcomes (duration of labor, mode of delivery, elective and emergency cesarean rates, postpartum hypertension and need for a blood transfusion, the admittance of the newborn into the intensive care unit, preferences for future births and duration of stay in hospital).

Enrollment: 70 patients

Sex: Female

Ages: 18 to 35 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Primiparas
• Ages between 18-35
• Lived in Aydın
• In gestational week 28-30,
• Pregnant with a single child
• Minimum a primary school graduate (since the questionnaires would be filled out by self-reporting)
• In a low-risk pregnancy (on the basis of the criteria of the Ministry of Health),
• Willing to divulge their own or their husband's telephone numbers,

Exclusion criteria

• High-risk pregnancy who had psychological and mental health problems
• History of infertility
• Speech and hearing disabilities
• Substance or narcotics users

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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70 participants in 2 patient groups

Intervention group

Experimental group

Description:

The study group were provided with individual counseling program and followed in this study, in addition to the usual care provided by healthcare professionals.

Treatment:

Behavioral: Intervention group

Control group

No Intervention group

Description:

The control group continued to receive the routine care