Investigation of the Effect of Supporting Nursing Care Provided in Line With During Intrapartum Period

Balikesir University

Status: Completed

Conditions: Delivery;Breech;Stillbirth

Treatments: Behavioral: supporting nursing care

Study type: Observational

Funder types: Other

Identifiers

NCT06024811

Balikesir

Details and patient eligibility

About

Aim: The aim of the research was to examine the effect of supportive nursing care provided in line with evidence-based practices during the intrapartum period.

Full description

Methods Design and Settings This study with intervention-control group, randomized and intervention type was carried out in a hospital in Balikesir, located in the west of Turkiye.

Hypotheses Hypothesis 1: Supportive nursing care provided in line with evidence-based practices during the intrapartum period has an effect on the state anxiety level of women.

Hypothesis 2: Supportive nursing care provided in line with evidence-based practices during the intrapartum period has an effect on perceived labor pain.

Hypothesis 3: Supportive nursing care provided in the intrapartum period in line with evidence-based practices has an effect on the duration on birth.

Hypothesis 4: Supportive nursing care provided in line with evidence-based practices in the intrapartum period has an effect on maternal satisfaction.

Universe and sample of the research

Enrollment: 1 patient

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Pregnant women over 18 years of age,
• with cervical dilatation 3 cm or more,
• Planned for spontaneous vaginal delivery,
• Term and singleton pregnancy,
• Who speak Turkish, who did not have language communication problems,
• Who voluntarily agreed to participate in the study were included

Exclusion criteria

• Pregnant women with head-pelvis incompatibility
• Those who gave birth by cesarean section before
• Pregnant women planned for cesarean delivery
• Pregnant women with any systemic disease (Diabetes mellitus, hypertension, etc.)
• Pregnant women who develop fetal distress or hypoxia during labor)

Trial design

1 participants in 2 patient groups

intervention

Description:

Pregnant women over 18 years of age, with cervical dilatation 3 cm or more, planned for spontaneous vaginal delivery, term and singleton pregnancy, who speak Turkish, who did not have language communication problems, and who voluntarily agreed to participate in the study were included. Pregnant women in the intervention and control groups were randomized using the "www.random.org website" on the computer (intervention=56 control= 56).Intervention and control groups were randomized according to some basic variables (age group, education level, body mass index, number of births and pregnancies, participation in prenatal preparation classes) considering the literature .

Treatment:

Behavioral: supporting nursing care

control

Description:

Pregnant women over 18 years of age, with cervical dilatation 3 cm or more, planned for spontaneous vaginal delivery, term and singleton pregnancy, who speak Turkish, who did not have language communication problems, and who voluntarily agreed to participate in the study were included. During the data collection period of the study, 313 women were evaluated according to the inclusion and exclusion criteria. Women who did not meet the inclusion criteria (n=198) and refused to participate in the study (n=3) were not included in the study sample. Pregnant women in the intervention and control groups were randomized using the "www.random.org website" on the computer (intervention=56 control= 56).Intervention and control groups were randomized according to some basic variables (age group, education level, body mass index, number of births and pregnancies, participation in prenatal preparation classes) considering the literature (Taghenijad et al. 2010; Erdogan et al. 2017).