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Labor Care Guide Application (LCG)

29. juni 2026 opdateret af: Ain Shams University

Labor Care Guide Application in Ain Shams University Maternity Hospital: A Randomized Controlled Trial

Application of the WHO Labor Care Guide in Ain Shams university Maternity hospital demonstrates high healthcare provider acceptability and improves labor progression, increases vaginal delivery rates, and reduces selected maternal complications without adversely affecting neonatal outcomes.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

The Labor Care Guide (LCG) is a tool developed by the World Health Organization (WHO) to support evidence-based, woman-centered intrapartum care and improve labor monitoring. It was introduced as an alternative to the traditional partograph, aiming to facilitate timely clinical decision-making and enhance the quality of maternity care.

This randomized controlled trial was conducted at Ain Shams University Maternity Hospital to evaluate the effect of the WHO Labor Care Guide on maternal and neonatal outcomes among women undergoing vaginal delivery. Eligible pregnant women were randomly assigned to one of two groups: a study group monitored using the WHO Labor Care Guide and a control group monitored using the modified WHO partograph.

Participants underwent routine obstetric assessment and monitoring throughout labor according to the allocated monitoring tool. Maternal outcomes assessed included labor progression, mode of delivery, and intrapartum and postpartum complications. Neonatal outcomes included neonatal well-being, need for neonatal intensive care admission, and neonatal complications. Healthcare provider satisfaction with the labor monitoring tool was also evaluated.

The study aimed to compare the effectiveness of the WHO Labor Care Guide with the modified WHO partograph in supporting labor management and improving maternal and neonatal care.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

350

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Cairo, Egypten
        • Ain Shams University Maternity Hospital

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  1. Pregnant woman who will undergo vaginal delivery at Ain Shams University Maternity Hospital with gestational age above or equal 37 weeks
  2. Vertex presentation .
  3. Women with estimated fetal weight 2.5 till 4 kg

Exclusion Criteria::

  1. Placenta previa
  2. Placenta previa accreta
  3. Macrosomic baby above 4 kg in diabetic women and above 4.5 kg in non diabetic women
  4. Placenta abruption complicated by non reassuring CTG or life threatening bleeding
  5. Cord prolapse
  6. Vasa previa
  7. Primary active genital herpes simplex
  8. Patient with anemia which may lead to atonic uterus and prolonged labor.
  9. Women with previously scarred uterus due to risk of ruptured uterus and postpartum hemorrhage

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Sundhedstjenesteforskning
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Labor care guide
Intervensional study
labor monitoring tool
Ingen indgriben: partogrph
no intervension

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Healthcare Provider Satisfaction as Measured by the Provider Satisfaction Questionnaire (PSQ)
Tidsramme: assessed at 6 months
Measured using a 5-point Likert scale. Range: 1-5. Higher scores indicate greater satisfaction.
assessed at 6 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Mode of delivery
Tidsramme: At delivery
The percentage of participants undergoing different modes of delivery (e.g., normal vaginal delivery, operative vaginal delivery, or cesarean section)
At delivery
Duration of active labor
Tidsramme: At delivery
The total duration of the active phase of labor, measured in hours.
At delivery
Incidence of maternal complications
Tidsramme: assessed at 6 weeks postpartum
The percentage of mothers who experience any postpartum or intrapartum complications (e.g., postpartum hemorrhage, infection).
assessed at 6 weeks postpartum
Incidence of neonatal complications
Tidsramme: At delivery
The percentage of newborns who experience neonatal complications (e.g., respiratory distress, hypoglycemia).
At delivery
Duration of hospital stay
Tidsramme: from birth until hospital discharge average 2 to 3 days
The total number of days the mother and/or neonate remained hospitalized from admission to discharge.
from birth until hospital discharge average 2 to 3 days
Neonatal Outcomes via Apgar Score and NICU Admission
Tidsramme: from birth until hospital discharge average 2 to 3 days
Neonatal well-being will be assessed using the Apgar score at 5 minutes (ranging from 0 to 10, where higher scores indicate better neonatal health) and the rate of admission to the Neonatal Intensive Care Unit (NICU).
from birth until hospital discharge average 2 to 3 days

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

1. april 2025

Primær færdiggørelse (Faktiske)

1. august 2025

Studieafslutning (Faktiske)

1. august 2025

Datoer for studieregistrering

Først indsendt

10. juni 2026

Først indsendt, der opfyldte QC-kriterier

29. juni 2026

Først opslået (Faktiske)

7. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

7. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

29. juni 2026

Sidst verificeret

1. august 2025

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Andre undersøgelses-id-numre

  • MS459

Plan for individuelle deltagerdata (IPD)

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UBESLUTET

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