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

Investigation of the Effect of Supporting Nursing Care Provided in Line With Evidence-Based Practices During Intrapartum Period

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06024811
Acronym
Support
Enrollment
1
Registered
2023-09-06
Start date
2020-09-03
Completion date
2021-02-15
Last updated
2023-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delivery;Breech;Stillbirth

Keywords

supportive nursing care, state anxiety.

Brief summary

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.

Detailed 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

Interventions

BEHAVIORALsupporting nursing care

Supportive nursing care was applied during the intrapartum period. Latent Active Transition phase,birt, postpartum period

Sponsors

Balikesir University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
positive birth2020-2021The positive birth highlights the importance of woman-centred care to optimize the experience of labour and childbirth for women and their babies through a holistic, human rights-based approach.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 21, 2026