Improving Nighttime Access to Care and Treatment; Part 4-Haiti
Recruiting
N/A
Interventional Study
Telemedicine
Pediatrics
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- Up to 10
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 7,124 (estimated)
- Sponsor
- University of Florida · Other
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About This Trial
Children in resource-limited settings who develop illness at night are often isolated from care, resulting in progression to an emergency. A telemedicine and medication delivery service (TMDS) is a viable healthcare delivery option to bridge the gap in nighttime care. This interrupted time series study (pre/post) will evaluate a digital clinical decision-support (dCDS) tool. The objective is to as…
Trial Locations
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Eligibility Criteria
Inclusion criteria for child, parent/guardian participants:
* Children 10 years of age or younger with an acute illness
* Parent/guardian contacts the TMDS in regards to the illness during hours of operation
* Parental/guardian agreement to a waiver of documentation of consent when contact is by ph…
Contacts