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NCT05506683Completed

Improving Nighttime Access to Care and Treatment; Part 2- Ghana

Pilot Implementation of a Nighttime Telemedicine and Medication Delivery Service to Increase Access to Pre-emergency Pediatric Care in Ghana

Source: ClinicalTrials.gov · Last updated 25 Sept 2025

Brief summary (registry, in English)

Globally, leading causes of death among children one month to 5 years old are pneumonia, diarrheal disease and malaria which are treatable early in the disease-course with low-cost medications. However, these diseases can progress to emergencies when access to care is delayed. In response, a telemedicine and medication delivery service (TMDS) was designed to improve nighttime access to pediatric care and treatment. The TMDS will be implemented in three distinct Ghanaian community to evaluate the clinical safety, operational feasibility of implementing,and scalability of the service.

Status (registry)
Completed
Study type
Interventional
Enrollment
1239 (actual)
First submitted
17 Aug 2022
Start date
16 Nov 2022
Primary completion date
1 Jul 2025
Lead sponsor
University of Florida
NCT number
NCT05506683

What you commit to

  • Study type: Interventional
  • Participants enrolled: 1239
  • From 16 Nov 2022 to the primary completion date, 1 Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Child Participant Inclusion Criteria:
  • Child ≤ 10 years
  • Has an acute medical problem
  • Provides written assent (if 10 years and receives a household visit)
    • Child Participant Exclusion Criteria:
  • Child \> 10 years
  • Child does not have an acute medical problem
  • Medical problem involves physical trauma or mental health
  • Refusal of written assent (if 10 years and receives a household visit)
    • Parent/Guardian Participant Inclusion Criteria:
  • Calls MotoMeds during operating hours
  • Parent/guardian of a patient participant meeting inclusion criteria
  • Adult (18 years or older)
  • Provides written consent (household visit) or a waiver of documentation of consent (no household visit)
    • Parent/Guardian Participant Exclusion Criteria:
  • Age \< 18 years
  • No written consent or waiver of documentation of consent
  • Corresponding child does not meet inclusion criteria

Age in the registry: - to 10 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Ambulance Service
Coordinator of this site? Confirm its status
AccraGhanaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.