Improving nighttime healthcare access for children in Haiti

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to enhance nighttime healthcare access for children in Haiti through a Telemedicine and Medication Delivery Service (TMDS) called MotoMeds. It evaluates the effectiveness of a digital clinical decision-support (dCDS) tool in improving adherence to treatment guidelines by TMDS providers. The study is based on previous research and involves assessing children under 10 years old who contact the service for acute illnesses. By analyzing pre- and post-implementation data, the study seeks to determine the impact of the dCDS tool on healthcare delivery in resource-limited settings.

Why it matters

Who can join: the full rules

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 phone only OR written consent/assent at the household from the parent/guardian and child (7yrs and older) for participants who receive a household visit.

Exclusion criteria for child, parent/guardian participants:

* No consent

Where it's running

• CV Foundation
  Gressier, Ouest, Haiti Recruiting

Study contacts

• Principal investigator: Eric J Nelson, MD PhD — University of Florida
• Study coordinator: Molly B Klarman, MPH
• Email: mklarman@ufl.edu
• Phone: 509 4600-7486

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.