A pilot multicentre cluster randomised trial to compare the effect of trauma life support training programmes on patient and provider outcomes

• Published in: BMJ open Vol. 12; no. 4; p. e057504
• Main Authors: Gerdin Wärnberg, Martin, Berg, Johanna, Bhandarkar, Prashant, Chatterjee, Anirban, Chatterjee, Shamita, Chintamani, Chintamani, Felländer-Tsai, Li, Gadgil, Anita, Ghag, Geeta, Hasselberg, Marie, Juillard, Catherine, Khajanchi, Monty, Kizhakke Veetil, Deepa, Kumar, Vineet, Kundu, Debabrata, Mishra, Anurag, Patil, Priti, Roy, Nobhojit, Roy, Amit, David, Siddarth, Singh, Rajdeep, Solomon, Harris, Soni, Kapil Dev, Strömmer, Lovisa, Tandon, Megha
• Format: Journal Article
• Language: English
• Published: England British Medical Journal Publishing Group 18.04.2022; BMJ Publishing Group LTD; BMJ Publishing Group
• Series: Protocol
• Subjects: accident & emergency medicine; Adults; Aged; Clinical outcomes; Consent; Curricula; Data collection; education & training (see medical education & training); Emergency medical care; Emergency Medicine; Female; Hospitals; Humans; India; Intervention; Male; Medicin och hälsovetenskap; Mortality; Patients; Physicians; Pilot Projects; Training; Trauma; Trauma care; trauma management; India; education & training (see medical education & training); accident & emergency medicine; trauma management
• ISSN: 2044-6055; 2044-6055
• DOI: 10.1136/bmjopen-2021-057504

IntroductionTrauma accounts for nearly 10% of the global burden of disease. Several trauma life support programmes aim to improve trauma outcomes. There is no evidence from controlled trials to show the effect of these programmes on patient outcomes. We describe the protocol of a pilot study that aims to assess the feasibility of conducting a cluster randomised controlled trial comparing advanced trauma life support (ATLS) and primary trauma care (PTC) with standard care.Methods and analysisWe will pilot a pragmatic three-armed parallel, cluster randomised controlled trial in India, where neither of these programmes are routinely taught. We will recruit tertiary hospitals and include trauma patients and residents managing these patients. Two hospitals will be randomised to ATLS, two to PTC and two to standard care. The primary outcome will be all-cause mortality at 30 days from the time of arrival to the emergency department. Our secondary outcomes will include patient, provider and process measures. All outcomes except time-to-event outcomes will be measured both as final values as well as change from baseline. We will compare outcomes in three combinations of trial arms: ATLS versus PTC, ATLS versus standard care and PTC versus standard care using absolute and relative differences along with associated CIs. We will conduct subgroup analyses across the clinical subgroups men, women, blunt multisystem trauma, penetrating trauma, shock, severe traumatic brain injury and elderly. In parallel to the pilot study, we will conduct community consultations to inform the planning of the full-scale trial.Ethics and disseminationWe will apply for ethics approvals to the local institutional review board in each hospital. The protocol will be published to Clinical Trials Registry—India and ClinicalTrials.gov. The results will be published and the anonymised data and code for analysis will be released publicly.