Background
A training system using Multi-platform ICT (MP-ICT) tools offers reliable and easier access to information and training packages from different locations which can be implemented even in rural settings without access to internet. Platforms may be available online, and users can download the training content through a personal computer, a tablet or a mobile phone. The training content may be downloaded repeatedly afterwards, even in remote areas without access to internet.
Our project aims to evaluate the performance of a continuous process of training and certification in neonatal resuscitation in primary and secondary health facilities in the departments of Ayacucho and Cusco, through the use of MP-ICT tools. It aims at providing proof of concept of the interventions, which then could be expected to be incorporated as a component of a national neonatal resuscitation program to be implemented nationwide.
The traditional way to train and certify health care professionals is through administration of a theoretical expositive course, reinforced subsequently by a practical component. This modality requires face-to-face contact between trainers and trainees. Health workers need to move from their job site to the instruction sites, usually located in the capital city of the department or in the capital city of the country. This poses economic and logistic challenges to both health authorities and health workers, and results in erratic frequency and low uptake of training courses.
Research hypothesis
The use of multi-platform ICT strategies for training and certification in neonatal resuscitation will increase the proportion of children with heart rate equal or greater than 100/minute at two minutes of life, as compared to standard training.
Primary objective
To evaluate the effects of the use of a Multi-Platform ICT strategies for training and certification on neonatal resuscitation in first and second level health facilities of Ayacucho and Cusco departments.
Settings
Ayacucho and Cusco are two Peruvian regions located to the south of the country. These regions cover areas of Andean highlands, but their territory is mainly on the Amazon rainforest. Also, in those departments there is the "Valley of the Apurímac, Ene and Mantaro Rivers", also known as the VRAEM, which is a geopolitical extremely poor area and one of the major areas of coca growing in Peru.
According to Peruvian Registry of Institutions that Provide Health Services (RENIPRESS), Ayacucho has 418 and Cusco 848 registered health facilities.
Study design
The proposed study design is a randomized cluster trial. The Units of study and analysis will be first and second level health facilities from Ayacucho and Cusco departments. Each health facility will be a cluster. Clusters will be randomly assigned either to the MP-ICT course and certification package (intervention) or to the standard training and certification package (control).
Sample size
The investigators would require 12 clusters (health facilities), divided in 6 clusters for each one of two arms, and with an average of 334 deliveries per facility in the observation period.
Assuming the occurrence of about 4,000 births during a period of 6 months of filed study observation, the investigators aim at discriminating a 4% difference in the proportion of newborns with heart rate equal or greater 100 beats per minute at 2 minutes of life between the intervention and the control group. The proposed power of study is 80% and the acceptable alpha error is 5%. The percentage for heart rate \>100 bpm at 2 minutes of life, during suitable resuscitation using self-inflated bag is 90% and it is the expected value for the intervention group. For the control group it is expected at least 4 points below the value achieved in the intervention group (i.e. no more than 86%).
Description of interventions
Standard Training
Standard training will be conducted through a theoretical-practical course, which will be administered once during the study period, to all health professionals of the selected facilities, according to the randomization. It is an 8-hour course, with 3 hours of theory (based on suggested readings) and 5 hours of practice, which will take place during a single day, approximately from 9:00 a.m. to 6:00 p.m according to the availability of the trained instructors and participants on suitable facilities for skills training. The course will be performed by staff of the Neonatal Unit of the Instituto Nacional de Salud del Niño (National Institute of Child Health, Lima, Peru), and will be coordinated by an Neonatal Resuscitation Program (NRP) instructor accredited by the American Academy of Pediatrics.
Participants who have completed their attendance to theoretical sessions, participated in the simulated practices and approved the printed exams taken the same day will grant a Standard Certification. The practice will be evaluated qualitatively in terms of assistance, participation and performance of activities.
Multi-platform ICT training
The continuous process of training and certification in neonatal resuscitation will be developed as a multi-platform format, including theory rechargeable online and accessible offline, and will be complemented with simulated practices. The Practical Component will be made after the Theoretical one and the activities will be completed according to the availability of the trained instructors and participants on suitable facilities for skills training.
The platform contains training packages, and links to review and download neonatal resuscitation tools, technical documents, and regulatory information. During the first three months of the project the platform is being improved and adjusted to the needs of the fieldwork in Ayacucho and Cusco. The adaptations include increasing hosting; ameliorate friendly usability, uploading packages and videos, improvement of examination and certifications, and tests for readiness. The MP-ICT resource will be user-friendly and can be accessed from remote locations through computers, personal portable devices and cell phones. It allows downloading of the different documents, and that facilitates learning and evaluation in an interactive and virtual way, without the physical presence of instructors or teachers. However, through the website the investigators can generate virtual meetings as forums or chat. In addition, the website will allow the programming of simulated practices, with the presence of the instructor.
Authorized participants will be able to download the information for the theoretical activities in 4 packages: Package A, B, C and D: each one containing interactive tools as videos-360 and action mazes (as Quandary), and other videos, documents or short text to read in Spanish. After downloading this information, the tests are enabled in sequence: When approve part A and B, it will be enable part C and D. The interactivity is expressed in 360º videos allowing the user to change the observation point in a recorded environment. The interactivity for action mazes (like Quandary) has demonstrated that feedback-oriented interactive exercises increase higher-order cognitive skills.
To be granted an MP-ICT Certification the trainee needs to have passed the online theoretical exam, assist to the practice and approve practical skills assessment.
Randomization
Computer-generated random numbers will be used to assign the selected health facilities to either MP-ICT training (Intervention Group) or to standard training (Control Group). There will be a matching process of health facilities by proportion of groups of non-medical professionals (nurses and obstetricians) and by availability of basic equipment and maternal and newborn care supplies, to ensure that health facilities are comparable. Once paired, they will be randomly allocated through a blocked randomization, to ensure a balanced distribution of facilities in each group.
Effectiveness assessment
After randomization of each facility, standard training or MP-ICT training will be conducted. Evaluations will include a baseline assessment of available equipment and supplies for neonatal resuscitation, immediately after enrolment and before training. To determine the duration of the effects of the intervention, the proposed outcome indicators will be evaluated six months after the training. The primary and secondary outcomes will be assessed intrapartum (within 5 minutes after birth) and postpartum (at 24 hours and 7 days, to know the outcome of the infant). The assessments will be based on an observation sheet, in which trained research assistants (registered nurses or equivalent local personnel) will record the activities conducted during the delivery and the birth, and the results of the neonatal resuscitation. The observation of performance in neonatal resuscitation can also be recorded randomly through videos, to verify the validity of the data collected by the research assistant. The videos will be reviewed by the field monitor and by one of the investigators. In order to comply with confidentiality requirements, the videos will be deleted after verification of information.
Statistical analysis
An intention to treat analysis will be performed, including all clusters as they were initially assigned, including premature withdrawals. Additionally, a per-protocol analysis will be carried out, where only clusters that have completed the study protocol will be considered. The primary outcome will be compared in each arm using chi-square if the variable of distribution is normal, or alternatively through the Fisher's exact test. Secondary outcomes will be compared using the Student's t-test or the Kruskal-Wallis test, the chi-square test or Fisher's exact test.
Staff training
The investigators will resort to local staff as research assistants including the field supervisor. They will conduct the preparatory work and the study procedures, including information presentations, informed consent administration, observation of case management, and completion of case report forms. Such personnel will be trained in the conduction of studies complying with the standards of good practice, before the study initiation.
Ethical aspects and confidentiality
The proposal, instruments and consent forms have been approved by the Ethics Committee of the Universidad Peruana Cayetano Heredia. Written authorization will be obtained from the authorities of the Regional Health Departments (DIRESAS) involved and from the authorities of the health facilities. Written informed consent will be obtained from the health professionals who will participate in the neonatal resuscitation training. Written informed consent of the mothers will also be obtained for the collection of birth and newborn data.
The information obtained will be codified and personal identification data like names and date of birth will be deleted to protect confidentiality. Data access will be limited to the Principal Investigator and authorized Co-Investigators. The study documents will be stored in locked environments at the Centro de Investigación para el Desarrollo Integral y Sostenible (CIDIS) at Universidad Peruana Cayetano Heredia to which access will be granted only to the Principal Investigator and the Co-Investigators authorized by the Principal Investigator.
