- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04504500
Reducing Cesarean Section Rates and Enhancing Vaginal Delivery in Greece: a Stepped-Wedge Randomized Controlled Trial (ENGAGE)
January 21, 2024 updated by: Hellenic Society of Obstetrics and Gynecology
Reducing the Cesarean Section Rates and Enhancing Vaginal Delivery in Greece Through Educational, Behavioral and Organizational Interventions in Labor Management: a Stepped-Wedge Randomized Controlled Trial (ENGAGE Trial)
It is becoming increasingly apparent that there is an urgent need to systematically investigate the rising cesarean section (CS) rates in Greece and develop interventions to substantially reduce these rates.
In this trial, to be conducted in Greece, the obstetricians will be exposed to educational, behavioral and/or organizational interventions while managing labor.
The trial is expected to yield new information about effective interventions to reduce unnecessary cesarean sections in Greece, hopefully leading the way to their reduction worldwide.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
- Behavioral: HSOG guidelines application
- Behavioral: Interactive workshops and courses
- Behavioral: Feedback through follow-up meetings
- Behavioral: Robson criteria usage
- Behavioral: Access to live real-time statistics
- Behavioral: Attendance of local cesarean section meetings
- Behavioral: Attendance of local CTG interpretation meetings
- Behavioral: Reminders of proper clinical practice
- Other: HSOG guidelines implementation
- Other: Interactive workshops and courses training
- Other: Implementation of Robson criteria classification
- Other: Live real-time statistics online platform
- Other: Local cesarean section meetings
- Other: Local CTG interpretation meetings
- Other: Follow-up meetings
Detailed Description
The present study explains the planned implementation of a stepped-wedge trial in Greek maternity units.
Twenty-two maternity units in Greece will participate in the trial involving 20,000 to 25,000 births, with two of the units entering the intervention period each month (stepped randomization).
The maternity units will apply the interventions for a period of 6-16 months, depending on the time they enter the intervention stage of the trial.
There will also be an initial baseline phase of the trial, lasting from 3 to 13 months; this phase will include observation and data collection of routine obstetric practices.
The interventions are based on educational, behavioral and organizational modifications and will include the implementation of the Hellenic Society of Obstetrics and Gynecology (HSOG) guidelines on labor management and targeted training in cardiotocography (CTG), obstetric emergencies, and the classification of cesarean section through Robson criteria.
During the trial period, the rates and indications for cesarean sections will be available to participating units on a live platform, using an anonymous reporting system.
Participating obstetricians will be able to see their own and other units' performance and also get feedback on their rates.
Τhe final three-month phase of the trial will be devoted to completion of questionnaires by the participating obstetricians.
The total estimated duration of the trial will be 22 months.
The primary outcome assessed will be the change in cesarean section rate and the secondary outcomes will be maternal and neonatal morbidity and mortality.
The intervention and control periods will be compared using mixed effects logistic regression with adjustment for any underlying secular trends.
Study Type
Interventional
Enrollment (Actual)
6029
Phase
- Not Applicable
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
-
-
-
Athens, Greece
- All participating units
-
-
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
14 years to 46 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- A minimum of 5 years' provision of obstetric services for the participating units.
- Top 22 units in Greece according to the number of deliveries and the type of unit (National Health System, private, university) and the unit's willingness to participate.
- Up to 11 obstetricians in each unit (based on the number of deliveries and their willingness to participate)
- Consent obtained from all participating professionals
- Consent obtained from all participating women
Exclusion Criteria:
- None
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
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Observation phase
Routine practice assessment
|
|
|
Active Comparator: Intervention phase
Clinical practice assessment after the application of the trial's educational, behavioral and organizational interventions
|
In their practice, as regards the mode of delivery, obstetricians are encouraged to conform to the three guidelines and two consent forms published by the Hellenic Society of Obstetrics and Gynecology (HSOG).
The members of the appointed Steering Committee and/or local opinion leaders will discuss and disseminate these guidelines among the professional staff in the respective maternity units, providing them with the opportunity to identify specific barriers, overcome them, and develop an implementation timetable.
The workshops and courses will give instruction in indications for cesarean section and clinical scenarios, physiology-based cardiotocography (CTG) interpretation, obstetric emergencies (with topics including breech delivery, trial of labor after cesarean, delivery of twins, induction and augmentation of labor), organization of the labor ward, as well as launching of regular cesarean section and CTG meetings with review of the patient notes.
The workshops will last four days and will be conducted by experienced trainers.
The expectation is that the obstetricians will gain very considerable knowledge and skills, which will enable them to subsequently follow these practices safely and competently.
Regular follow-up meetings with members of the steering committee and local opinion leaders throughout the intervention period will enhance compliance with the guidelines.
Feedback with positive phrasing will be incorporated to meet local needs.
Obstetricians are set to a routine to enable them to use the Robson 10-group classification criteria for cesarean sections and obtain feedback on the unit's cesarean section rates monthly.
They thus know which category is higher and can be reduced further.
Live real-time statistics provided by an online platform, on a regular basis, is expected to improve adherence, through regular feedback.
Each unit will see other units' statistics by means of an anonymous reporting system.
This repetition will create silent signals that will remind the participating obstetricians to remain on task.
Local cesarean section meetings will be held weekly, in each unit.
The members of the steering committee or local opinion leaders may actively participate in these meetings.
Local obstetricians learn to judiciously adapt standard medical practices, thereby avoiding unnecessary medical interventions.
This is a way to further enhance compliance, as during the discussions the behavior expected of the obstetricians is clearly stated by the participating opinion leaders.
Local CTG interpretation meetings will be held weekly, in each unit, during which all "abnormal" CTG cases that led to cesarean section will be reviewed and discussed.
Members of the Steering Committee or local opinion leaders may actively participate in these meetings.
Obstetricians are encouraged to reflect on their medical practice through judicious physiology-based CTG interpretation.
Effective and reliable reminders concerning optimal obstetric practice will be placed in labor wards, staff rooms, patient notes, vaginal birth packages and above theater hand washers.
There will be short messages with positive phrasing regarding the benefits of vaginal birth, thus reminding birth attendants to reduce unnecessary cesarean sections.
Relevant SMS (short message service) will be sent to the participating obstetricians' mobiles on a regular basis, so as to motivate them via non-verbal signals.
There will be application in daily practice of three guidelines and two consent forms pertaining to the mode of delivery published by HSOG.
Obstetricians are informed on evidence-based medicine in obstetrics and provided with a structured and safe approach to labor management.
The members of the appointed Steering Committee and/or local opinion leaders discuss and disseminate the guidelines among the professional staff at the respective maternity units, answer questions, and make available their knowledge and experience.
Adoption of guidelines by the participating unit helps to establish clear, consistent rules that are direct and simple, and obstetricians are asked to embrace fully justified medical practice.
Other Names:
The workshops and courses will provide instruction in indications for cesarean section and case scenarios, physiology-based CTG interpretation, obstetric emergencies (with topics including breech delivery, trial of labor after cesarean, delivery of twins, induction and augmentation of labor), organization of labor ward and launching of cesarean section and CTG meetings.
This type of formal training provides problem-solving strategies, using mnemonics, that are critical in emergencies and that also aid in learning and retaining the skills being taught.
Functional and social skills that directly affect decision-making and effectiveness are addressed.
Thus, units adopt a continuous educational procedure for their staff, enhancing their confidence when dealing with labor emergencies and redesigning labor management plans, so as to ensure high-level obstetric services.
Other Names:
Use will be implemented of an online application embedded in the REDCap electronic database questionnaire with Robson 10-group classification criteria and feedback on the unit's cesarean section rates monthly, so as to know which category is higher and can be reduced further.
This change in the unit's practice will introduce a new medical reporting and audit system that can detect unjustified medical procedures much more easily.
Other Names:
Live real-time statistics provided on a regular basis by an online platform will provide feedback and essential information.
Each unit will see other units' statistics using an anonymous reporting system.
This information can trigger self-generative learning strategies and help obstetricians to become more effective learners.
Other Names:
Local cesarean section meetings will be held weekly in each unit.
The members of the Steering Committee or local opinion leaders may actively participate in these meetings.
The unit's staff can hear about both justified and unnecessary surgical procedures and draw informed conclusions as to the optimal procedure in similar cases.
They will also have the opportunity to actively participate in an elaborative problem-solving discussion.
These meetings when routinely conducted, provide feedback and audit resources to help improve performance and further enhance compliance.
Other Names:
Local CTG interpretation meetings will be held weekly, in each unit during which all "abnormal" CTG cases that led to cesarean section will be reviewed and discussed.
Members of the Steering Committee or local opinion leaders may actively participate in these meetings offering coaching and counseling services in decision-making.
Through elaborative discussion the staff will improve their knowledge and skills in correct CTG interpretation, thus preventing unnecessary interventions, such as cesarean sections.
Other Names:
Regular follow-up meetings of the participating obstetricians with members of the steering committee and local opinion leaders throughout the intervention period will enhance compliance with the guidelines.
Establishment of commonly accepted practice augments the homogeneity of clinical action plans and team work in the unit.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cesarean section rate
Time Frame: Admission to maternity unit to time of vaginal or cesarean birth
|
Number of cesarean section deliveries in the study period divided by the number of live vaginal and cesarean births
|
Admission to maternity unit to time of vaginal or cesarean birth
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maternal morbidity
Time Frame: During labor and 40 days to 3 months after delivery
|
Incidence of maternal complications in labor and postpartum
|
During labor and 40 days to 3 months after delivery
|
|
Perinatal and neonatal morbidity
Time Frame: During labor and 40 days to 3 months after delivery
|
Incidence of perinatal and neonatal complications in labor and postpartum
|
During labor and 40 days to 3 months after delivery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Nikolaos Vrachnis, Prof Ob/Gyn, Hellenic Society of Obstetrics and Gynecology
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.
General Publications
- Hussey MA, Hughes JP. Design and analysis of stepped wedge cluster randomized trials. Contemp Clin Trials. 2007 Feb;28(2):182-91. doi: 10.1016/j.cct.2006.05.007. Epub 2006 Jul 7.
- Betran AP, Ye J, Moller AB, Zhang J, Gulmezoglu AM, Torloni MR. The Increasing Trend in Caesarean Section Rates: Global, Regional and National Estimates: 1990-2014. PLoS One. 2016 Feb 5;11(2):e0148343. doi: 10.1371/journal.pone.0148343. eCollection 2016.
- Betran AP, Torloni MR, Zhang JJ, Gulmezoglu AM; WHO Working Group on Caesarean Section. WHO Statement on Caesarean Section Rates. BJOG. 2016 Apr;123(5):667-70. doi: 10.1111/1471-0528.13526. Epub 2015 Jul 22. No abstract available.
- Vrachnis N, Vlachadis N, Iliodromiti Z, Vlachadi M, Creatsas G. Greece's birth rates and the economic crisis. Lancet. 2014 Feb 22;383(9918):692-3. doi: 10.1016/S0140-6736(14)60252-X. No abstract available.
- Vlachadis N, Vrachnis N, Economou E. Fertility treatments and multiple births in the United States. N Engl J Med. 2014 Mar 13;370(11):1069-70. doi: 10.1056/NEJMc1400242. No abstract available.
- Vlachadis N, Iliodromiti Z, Creatsas G, Vrachnis N. Preterm birth time trends in Europe: the worrying case of Greece. BJOG. 2014 Feb;121(3):372-3. doi: 10.1111/1471-0528.12529. No abstract available.
- The Lancet. Stemming the global caesarean section epidemic. Lancet. 2018 Oct 13;392(10155):1279. doi: 10.1016/S0140-6736(18)32394-8. No abstract available.
- Vrachnis N, Iliodromiti S, Samoli E, Iliodromiti Z, Dendrinos S, Creatsas G. Maternal mortality in Greece, 1996-2006. Int J Gynaecol Obstet. 2011 Oct;115(1):16-9. doi: 10.1016/j.ijgo.2011.04.014. Epub 2011 Jul 23.
- Chen I, Opiyo N, Tavender E, Mortazhejri S, Rader T, Petkovic J, Yogasingam S, Taljaard M, Agarwal S, Laopaiboon M, Wasiak J, Khunpradit S, Lumbiganon P, Gruen RL, Betran AP. Non-clinical interventions for reducing unnecessary caesarean section. Cochrane Database Syst Rev. 2018 Sep 28;9(9):CD005528. doi: 10.1002/14651858.CD005528.pub3.
- Vrachnis N, Vlachadis N. Maternal mortality estimates. Lancet. 2014 Dec 20;384(9961):2210. doi: 10.1016/S0140-6736(14)62423-5. Epub 2014 Dec 19. No abstract available.
- Vlachadis N, Vrachnis N, Tsikouras P, Mastorakos G, Iliodromiti Z. Birth rates by maternal age in Greece: background, trends and future perspectives. J Reprod Med. 2015 Mar-Apr;60(3-4):183-4. No abstract available.
Helpful Links
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)
May 31, 2021
Primary Completion (Actual)
August 31, 2023
Study Completion (Actual)
October 31, 2023
Study Registration Dates
First Submitted
August 5, 2020
First Submitted That Met QC Criteria
August 5, 2020
First Posted (Actual)
August 7, 2020
Study Record Updates
Last Update Posted (Estimated)
January 23, 2024
Last Update Submitted That Met QC Criteria
January 21, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 129/29062018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Study data may be shared upon chief investigator's decision after reasonable request and up to 8 year after the conclusion of the trial.
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.
Clinical Trials on Cesarean Section Rates
-
Massachusetts General HospitalMbarara University of Science and TechnologyActive, not recruiting
-
Sohag UniversityActive, not recruitingCaesrean Section Rates | Robson ClassificationEgypt
-
Assiut UniversityNot yet recruitingCesarean Section Complications | Cesarean Section Niche
-
Kutahya Health Sciences UniversityCompletedPregnancy | Cesarean Section | Elective Cesarean SectionTurkey (Türkiye)
-
Recep Tayyip Erdogan University Training and Research...CompletedCesarean Section Complications | Cesarean Section; DehiscenceTurkey
-
Ataturk UniversityUnknownCesarean Section Complications | Cesarean Section; Complications, Wound, Dehiscence | Cesarean Section, Repeated | Cesarean, Uterine Scar Thickness | Cesarean, Residual Myometrial ThicknessTurkey
-
Asfendiyarov Kazakh National Medical UniversityCenter for Perinatology and Pediatric Surgery, Almaty, Kazakhstan; Zhalyn Scientific...RecruitingSkin Wound Healing After Cesarean Section | Cesarean Section Scar HealingKazakhstan
-
Odense University HospitalHvidovre University Hospital; Smith & Nephew, Inc.; University of Southern Denmark and other collaboratorsCompletedSurgical Wound Infection | Cesarean Section; Dehiscence | Complications; Cesarean Section | Infection; Cesarean Section | Complications; Cesarean Section, Wound, Dehiscence | Wound; Rupture, Surgery, Cesarean SectionDenmark
-
Kanuni Sultan Suleyman Training and Research HospitalCompletedCesarean Section Complications | Cesarean Section; DehiscenceTurkey
-
Chiayi Christian HospitalNot yet recruiting
Clinical Trials on HSOG guidelines application
-
Nantes University HospitalSociété Française d'Anesthésie et de RéanimationCompletedPneumonia | Sepsis | Ventilator-Associated Pneumonia | Hospital Acquired PneumoniaFrance
-
Hospices Civils de LyonCompleted
-
Complement Theory Inc.Active, not recruitingBreast Cancer | Colorectal Cancer | Lung Cancer | Prostate Cancer | Other CancerUnited States
-
University College DublinQueen's University, Belfast; University College Cork; TeagascCompletedDietary Habits | Healthy Diet | Healthy Nutrition | Personalized NutritionIreland, United Kingdom
-
Pennington Biomedical Research CenterCompleted
-
The University of Texas Health Science Center,...Not yet recruitingFetal Growth RetardationUnited States
-
University of ArizonaCompletedTBI (Traumatic Brain Injury) | Brain Injuries, Traumatic | Injuries, Acute BrainUnited States
-
Johns Hopkins UniversityCompletedLatent TuberculosisUnited States
-
Institut National de la Santé Et de la Recherche...CompletedFrench PNNS Guidelines in Vascular Function
-
Rabin Medical CenterUnknown