Cardiac Arrest Clinical Trials

Find Cardiac Arrest Clinical Trials Near You

Evaluation of an Enhanced Community First Responder Support System to Improve Bystander Cardiopulmonary Resuscitation Quality for Patients Experiencing Out-of-hospital Cardiac Arrest

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The rise in out-of-hospital cardiac arrest (OHCA) cases in Singapore highlights the need for effective bystander cardiopulmonary resuscitation (BCPR). Despite many lay responders performing CPR, survival rates with good neurological outcomes have not significantly improved, prompting research into the quality of CPR as a critical factor. The study by Gallagher EJ et al. showed a significant survival improvement with high-quality CPR. To address this, the Unit of Pre-hospital and Emergency Research (UPEC) trained thousands of community first responders (CFRs) in simplified CPR techniques using hands-only and DA-CPR methods. A significant innovation is the CPRcard®, developed by Laerdal in Norway, which offers real-time feedback on the quality of chest compressions. However, only 36% of CFRs using the CPRcard® achieved the desired compression standards, indicating room for improvement. The study proposes enhancing CFR support with information communication technology (ICT), enabling two-way audio and one-way video communication between CFRs and dispatchers. This aims to reduce stress among responders, increase their willingness to engage with OHCA alerts, and improve CPR quality. The clinical trial in Singapore will compare the current system against the enhanced CFR support system (eCSS), focusing on the real-time relay of CPR performance data, communication ease, and implementation factors. The high-quality CFR and OHCA registries in Singapore provide a robust setting for this research, aiming to enhance CPR delivery and improve OHCA outcomes through technology and real-time support.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 21
Healthy Volunteers: t
View:

• 18 years old and above

• SCDF registered CFRs

• Trial dispatchers with an active account of myResponder® app on their mobile phones

Locations
Other Locations
Singapore
Duke-NUS Medical School
RECRUITING
Singapore
Contact Information
Primary
Fahad J Siddiqui, MSc
fahad.siddiqui@duke-nus.edu.sg
+6566017951
Backup
Alexander A White, MSc
alexander.elgin.white@upec.sg
+65 90674081
Time Frame
Start Date: 2024-08-01
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 165
Treatments
Active_comparator: SoC
Standard of Care
Experimental: eCSS
enhanced CFR support system (eCSS)
Related Therapeutic Areas
Sponsors
Leads: Singapore General Hospital
Collaborators: Duke-NUS Graduate Medical School

This content was sourced from clinicaltrials.gov