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

Sponsor
Balikesir University (Other)
Overall Status
Completed
CT.gov ID
NCT06024811
Collaborator
(none)
1
1
5.4
0.2

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: supporting nursing care

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

Study Design

Study Type:
Observational
Actual Enrollment :
1 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Investigation of the Effect of Supporting Nursing Care Provided in Line With Evidence-Based Practices During Intrapartum Period
Actual Study Start Date :
Sep 3, 2020
Actual Primary Completion Date :
Dec 15, 2020
Actual Study Completion Date :
Feb 15, 2021

Arms and Interventions

Arm Intervention/Treatment
intervention

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 .

Behavioral: supporting nursing care
Supportive nursing care was applied during the intrapartum period. Latent Active Transition phase,birt, postpartum period
Other Names:
  • Supportive nursing care practices in the latent phase Types of supportive care Physical Emotional Informational Advocacy Partner
  • control

    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).

    Outcome Measures

    Primary Outcome Measures

    1. positive birth [2020-2021]

      The 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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts 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)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Balıkesir University Balıkesir Altıeylül Turkey 10100

    Sponsors and Collaborators

    • Balikesir University

    Investigators

    • Principal Investigator: ESRA ÇEVİK, https://akademik.yok.gov.tr/AkademikArama/view/viewAuthor.jsp

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Esra Cevik, Assist Prof., Balikesir University
    ClinicalTrials.gov Identifier:
    NCT06024811
    Other Study ID Numbers:
    • Balikesir
    First Posted:
    Sep 6, 2023
    Last Update Posted:
    Sep 6, 2023
    Last Verified:
    Aug 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Esra Cevik, Assist Prof., Balikesir University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 6, 2023