Patients Acceptance Towards Elective Labor in Induction (PALI) (PALI)

August 4, 2022 updated by: Hanoi Obstetrics and Gynecology Hospital

Patients Acceptance Towards Elective Induction of Labor at 39th Week of Gestation (PALI)

To assess patients' preference, understanding regarding elective IOL and factors contribute to decision making process towards elective IOL at 39th week of gestation.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

A normal pregnancy lasts between 37+0 to 41+6 weeks. Estimated date of delivery is set exactly at 40+0 weeks of gestation. Base on this estimation, professional society's guidelines have recommended to start inducing the labor from 41+0 to 41+6 weeks after the last menstrual period. Clinical practice during the last few decades has been moving towards this trend and postponing labor induction.

But is 40 weeks' gestational age the optimal endpoint of human pregnancy? Recent studies, however, showed different results where many of them support induction of labor at 39 weeks. A large cohort retrospective study which included information from merely 5.4 million non-anomalous live births in the United States from 2012 to 2016, though only modestly, the authors have been able to conclude that the rates of composite neonatal and maternal adverse outcomes increase from 39 through 41 weeks of gestation among low-risk parous women. Stratifying by parity, it seemed that the trend is also similar among all low-risk women no matter which parities they are in. When it comes to nulliparous women, results from a large prospective randomized control trial (the ARRIVE trial) show that induction of labor at 39 weeks in low-risk nulliparous women did not lead to significant lower frequency of a composite adverse perinatal outcome but it did result in a significant lower rate of cesarean delivery. More recently, in a review sponsored by the Cochrane library on induction of labor beyond 37 weeks' gestation has found that there is a clear reduction in perinatal death with a policy of labor induction at or beyond 37 weeks compared with expectant management, though absolute rates are small (0.4 versus 3 deaths per 1000). There were also lower caesarean rates without increasing rates of operative vaginal births and there were fewer Neonatal Intensive Care Unit admissions with a policy of induction. Base on these evidence, the American College of Obstetricians and Gynecologists has suggested "it's time to induce of labor at 39th week of gestation". It is true that although induction of labor is familiar with obstetricians, the procedure is still raising concern from patients' side. Even in the United States where patients consulting has been routinely applied, the rate of patients refuse to be induced at 39th week of gestation is about 50%. Review from Cochrane library also suggested that "Offering women tailored counselling may help them make an informed choice between induction of labor for pregnancies" . In some countries where the National Guidelines still recommends induction of labor should be considered after 41 weeks of gestation and pregnancy related decisions are driven by many identical factors such as: knowledge, traditional or cultural ones, the patients' perspective on induction of labor before 40 weeks of gestation is a challenge. Thus, the patients' understanding of the elective induction of labor and factors contribute to decision-making process towards induction of labor should be investigated in order not only to develop appropriate induction policies for the future but also scientific studies/randomized clinical trials to come.

Study Type

Observational

Enrollment (Actual)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hà Nội
      • Hanoi, Hà Nội, Vietnam, 10000
        • Hanoi Obstetrics and Gynecology Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Low risk pregnant women with a gestational age at 36th week and 39th weeks

Description

Inclusion Criteria:

  • Maternal age ≥ 18
  • Singleton pregnancy (twin gestation reduced to singleton, either spontaneously or therapeutically, is not eligible unless the reduction occurred before 14 weeks project gestational age)
  • Gestational age at 36+0 weeks to 36+6 week
  • Cephalic presentation
  • No contraindications to vaginal delivery

Exclusion Criteria:

  1. Previous C-section
  2. Maternal medical illness associated with increased risk of adverse pregnancy outcome (any diabetes mellitus, any hypertensive disorders, cardiac diseases, renal insufficiency, systemic lupus erythematosus, mental disorders, HIV positive, use of heparin or low-molecular weight heparin during the current pregnancy etc.)
  3. Abnormal placenta: Active vaginal bleeding greater than bloody show or placenta previa, accreta or vasa previa
  4. Abnormal amniotic fluid volume:

    Oligohydramnios (MVP < 2cm) Polyhydramnios (MVP > 10cm)

  5. Abnormal fetus Fetal demise or known major fetal anomalies Fetal growth restriction (FGR) (EFW < 3% or < 10% and abnormal Doppler) Non-reassuring fetal status (no fetal movements, abnormal fetal heart rate at auscultation)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of patients accept to undergo elective induction of labor at 39th gestational week
Time Frame: It is planned to fill the questionnaire in 30 minutes at 39th gestational week
Number of patients who are willing to undergo elective Induction of labor without maternal of fetal indication at 39th gestational week
It is planned to fill the questionnaire in 30 minutes at 39th gestational week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Participants knowledge
Time Frame: It is planned to fill the questionnaire in 30 minutes at 36th gestational week
Description of knowledge and opinions of participants towards induction of labor The knowledge about induction of labor, consisted of 13 multiple choice questions including different methods, indications, contraindications, maternal and fetal benefits/ risks of induction of labor.
It is planned to fill the questionnaire in 30 minutes at 36th gestational week
Participants opinions
Time Frame: It is planned to fill the questionnaire in 30 minutes at 36th gestational week
Opinion about the needs for induction of labor, consisted of 12 questions including different reasons for labor induction. Participants choose the level of agreement (strongly disagree; disagree; support; strongly support) for each questions.
It is planned to fill the questionnaire in 30 minutes at 36th gestational week
Reasons to choose or refuse elective induction of labor at 36th gestational week
Time Frame: It is planned to fill the questionnaire in 30 minutes at 36th gestational week
Reasons why participants choose or refuse elective induction of labor: a checklist (yes/no) of 14 reasons and an open-end question
It is planned to fill the questionnaire in 30 minutes at 36th gestational week
Reason why participants change initial decision about elective induction of labor
Time Frame: It is planned to fill the questionnaire in 30 minutes at 39th gestational week
Reason why participants change decision about elective induction of labor: a checklist (yes/no) of 14 reasons and an open-end question
It is planned to fill the questionnaire in 30 minutes at 39th gestational week
Factors that may affect participants' decision
Time Frame: It is planned to fill the questionnaire in 30 minutes at 36th gestational week
Factors that may affect participants' decision towards elective induction of labor: multiple choice questions regarding the age, ethnic group, education background, profession, financial ability, residential and cohabitation arrangement, healthcare preferences of participants
It is planned to fill the questionnaire in 30 minutes at 36th gestational week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Ha Nguyen Thi Thu, PhD. MD, Hanoi Obstetric and Gynecology Hospital
  • Principal Investigator: Minh Chau Ngoc, MD, Mỹ Đức Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 15, 2021

Primary Completion (Actual)

March 15, 2022

Study Completion (Actual)

June 30, 2022

Study Registration Dates

First Submitted

January 22, 2021

First Submitted That Met QC Criteria

February 2, 2021

First Posted (Actual)

February 3, 2021

Study Record Updates

Last Update Posted (Actual)

August 5, 2022

Last Update Submitted That Met QC Criteria

August 4, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • PSHN.0002.2021

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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