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Completed

NCT Number: NCT01681017

Global Network Implementation of Helping Babies Breathe (HBB)

The primary purpose of this pre-post evaluation is to test the impact on perinatal mortality (fresh stillbirths or early neonatal deaths) among births > 1500g of training birth attendants at health facilities in the Helping Babies Breathe (HBB) and Essential Newborn Care (ENC) curricula. These facilities are located within clusters in the Global Network for Women's and Children's Health Research sites in Belgaum and Nagpur, India, and Eldoret, Kenya.

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Jawaharlal Nehru Medical College, Belagavi, India

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About this study

Helping Babies Breathe (HBB) is a training program designed to resuscitate neonates regardless of where they were born. HBB was developed by the American Academy of Pediatrics (AAP), the NICHD's Global Network for Women's and Children's Health (GN), the Laerdal Foundation and their global partners. The HBB program was developed based upon the experience and results of an earlier Neonatal Resuscitation Program and the GN's FIRST BREATH randomized control trial.

The goal of the study is to test the impact of training birth attendants at selected health facilities in the Helping Babies Breathe (HBB) and Essential Newborn Care (ENC) curricula upon perinatal mortality (fresh stillbirths and early neonatal deaths), among births of ≥1500g. The training will take place in three GN sites, Kenya, and Nagpur and Belgaum, India. The study facilities serve the population in identified study clusters, defined geographic areas which participate in the GN's Maternal Newborn Health (MNH) Registry. In addition to measuring perinatal mortality rate pre and post training, the study will also assess resuscitation skills among the birth attendants as a result of the training. Quality Improvement activities are planned to ensure the integrity of the training, maintenance and availability of resuscitation equipment and skills maintenance.

The GN MNH Registry (NCT 01073475) was established in 2008 and includes all pregnancies and neonatal outcomes in defined geographic clusters. The primary outcome for the pre-post HBB evaluation study will be calculated using all delivery data from the GN MNH Registry for participating clusters during the defined study period.

The pre-post HBB evaluation will include the following key activities:

  • Selection of Master Trainers, Facilitators, and Learners
  • Country-level training of Master Trainers in the HBB and ENC curricula
  • Facility-level training of birth attendants in the HBB and ENC curricula
  • Periodic re-training of birth attendants in the HBB and ENC curricula
  • Quality improvement activities:
  • Regular observation of deliveries in participating study health facilities
  • Unannounced observation of deliveries (or HBB skills using a neonatal simulator if no deliveries are available)
  • Resuscitation debriefings
  • Perinatal Death audits
  • Daily bag and mask ventilation practice
  • Drills to practice emergency drills
  • Daily check of cleanliness and availability of resuscitation equipment.

The HBB Master Trainers (MT), Facilitators, and Learners will be evaluated at several points during the implementation of the training program and quality improvement activities.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Facilities:
  • at least 60 deliveries per year;
  • ability to provide 24-hour coverage, 7 days per week in the delivery ward; and
  • minimum perinatal mortality rate of 30 per 1000 deliveries in the reference period.

Master Trainers (MT)

  • Experienced teachers and content experts in neonatal resuscitation
  • Trained and/or experienced in education
  • Dedication to learner-focused education
  • Able to give informed consent

Facilitators

  • Experienced in teaching Learners in small groups
  • Experienced in care of newborns
  • Demonstrated understanding of course content
  • Aptitude for teaching
  • Able to give informed consent

Learners

  • Skilled birth attendants with clearly defined responsibilities for attending deliveries at participating facilities
  • Able to give informed consent

Exclusion criteria

  • If a facility, master trainer, facilitator, or learner does not meet the above inclusion criteria they are excluded from the study.

Treatment and study plan

HBB/ENC Training and Equipment

Behavioral

See the detailed description section

HBB/ENC supplies

Other

Staffs associated with participating facilities receive HBB/ENC training and use related equipment.

Primary outcomes

  1. Perinatal Mortality

    Time frame: Perinatal mortality data collected at 6 weeks post-delivery. Comparison will include the pre-intervention period of 12 months and the post-intervention period of 12 months.

    The difference in the rate of perinatal mortality (fresh stillbirth or neonatal death prior to 7 days) among births ≥1500g, pre versus post implementation of an integrated package of HBB and ENC training and equipment (referred to as HBB/ENC training and equipment). This measure will be calculated using delivery data from the Global Network's Maternal Newborn Health Registry for participating clusters.

Secondary outcomes

  1. Facility-based perinatal mortality

    Time frame: Perinatal mortality data collected at 6 weeks post-delivery. Comparison will include the pre-intervention period of 12 months and the post-intervention period of 12 months.

    The difference in the rate of facility-based perinatal mortality, among births ≥1500g pre versus post implementation of HBB/ENC training and equipment.

  2. Retention of resuscitation knowledge and skills

    Time frame: Assessments completed at initial training and refresher training.

    The difference pre versus post intervention in mean scores on a multiple choice test of resuscitation knowledge, observed skills in bag and mask ventilation (BMV), and OSCE A and OSCE B scenarios.

  3. Number of neonatal resuscitations

    Time frame: Resuscitation data collected at 6 weeks post-delivery.

    The difference in the number of neonatal resuscitations, among births ≥1500g with bag and mask in participating facilities pre versus post HBB/ENC training and equipment.

  4. Delivery room checklist score

    Time frame: Observations conducted on a monthly basis.

    The difference in scores on delivery room checklist (in facilities with > 100 deliveries/year)

  5. Asphyxia related perinatal mortality

    Time frame: Perinatal mortality data collected at 6 weeks post-delivery. Comparison will include the pre-intervention period of 12 months and the post-intervention period of 12 months.

    The difference in the rate of asphyxia related perinatal mortality, among births ≥1500g pre versus post HBB/ENC training.

  6. Health seeking behavior

    Time frame: Data collected at 6 weeks post-delivery. Comparison will include the pre-intervention period of 12 months and the post-intervention period of 12 months.

    The difference in the proportion of health seeking behavior pre versus post HBB/ENC training.

  7. Facility deliveries

    Time frame: Data collected at 6 weeks post-delivery. Comparison will include the pre-intervention period of 12 months and the post-intervention period of 12 months.

    The difference in the proportion of facility deliveries pre versus post HBB/ENC training.

  8. Very early newborn death (within 1 day of birth)

    Time frame: Data collected at 6 weeks post-delivery. Comparison will include the pre-intervention period of 12 months and the post-intervention period of 12 months.

    The difference in very early newborn death (within 1 day of birth) pre versus post HBB/ENC training.

Sponsors and collaborators

Lead sponsor

NICHD Global Network for Women's and Children's Health

Network

Collaborators

  • Christiana Care Health Services
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • Indiana University
  • Jawaharlal Nehru Medical College
  • Laerdal Medical
  • Lata Medical Research Foundation, Nagpur
  • Massachusetts General Hospital
  • Moi Univeristy
  • RTI International

Registry information

Official study title

Global Network for Women's and Children's Health Research Does Implementation of HELPING BABIES BREATHE (HBB) Save Lives?

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Sep 7, 2012
Registry last updated
Oct 14, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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