Objective
To evaluate the effectiveness of the Welch Allyn Connex
®
Spot Monitor/Hillrom Connecta™ solution in activating the rapid
response team in a timely manner compared to manual activation.
Methods
The Hillrom study is a single-center, open-label, superiority,
cluster-randomized, parallel-group (1:1 allocation ratio) clinical trial
that will be conducted in a tertiary hospital. Two sets of three wards with
28 beds will be included (one as the intervention cluster and the other as
the control). The wards will be randomly assigned to use the Welch Allyn
Connex
®
Spot Monitor/Hillrom Connecta™
automated solution (intervention cluster) or to maintain the usual routine
(control cluster) regarding rapid response team activation. The primary
outcome will be the absolute number of episodes of rapid response team
triggering in an appropriate time; as secondary outcomes, clinical features
(mortality, cardiac arrest, need for intensive care unit admission and
duration of hospitalization) will be assessed according to clusters in an
exploratory way. A sample size of 216 rapid response team activations was
estimated to identify a possible difference between the groups. The protocol
has been approved by the institutional Research Ethics Committee.
Expected results
The Welch Allyn Connex
®
Spot Monitor/Hillrom
Connecta™ automated solution is expected to be more effective in
triggering the nurse call system to activate the rapid response team in a
timely and adequate manner compared to manual triggering (usual
practice).
ClinicalTrials.gov
NCT04648579