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Enhanced Community First Responder System Evaluation in Singapore (TCPR-Link)

S

Singapore Health Services (SingHealth)

Status

Invitation-only

Conditions

Out-Of-Hospital Cardiac Arrest

Treatments

Device: CPRCard + TCPR Link App and Web
Device: CPRCard Only

Study type

Interventional

Funder types

Other

Identifiers

NCT06530433
CIRB 2015-2475

Details and patient eligibility

About

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.

Enrollment

165 estimated patients

Sex

All

Ages

21+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years old and above
  • SCDF registered CFRs
  • Trial dispatchers with an active account of myResponder® app on their mobile phones

Exclusion criteria

  • The CFRs who are pregnant
  • Experiencing any serious physical Conditions
  • Mental Health Conditions

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

165 participants in 2 patient groups

SoC
Active Comparator group
Description:
Standard of Care
Treatment:
Device: CPRCard Only
eCSS
Experimental group
Description:
enhanced CFR support system (eCSS)
Treatment:
Device: CPRCard + TCPR Link App and Web

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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