Clinical trial Recruiting at 1 site Interventional Ages 3 to 18

Continuous vital signs monitoring using a consumer wearable in Ghana hospitals

Official title: Implementing a Hospital-based Continuous Patient Monitoring System Using Consumer Wearable Devices in Ghana

Run by University of Alabama at Birmingham · NCT06739447 · Data updated 2026-11-12

This study tests whether a consumer wearable (Garmin Venu 3) can be used to continuously track heart rate, oxygen saturation, and breathing in pediatric trauma and post-appendectomy patients to catch deterioration earlier.

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Quick facts

Study typeInterventional
Ages3 Years to 18 Years
SexAll
Enrollment250 (estimated)
SponsorUniversity of Alabama at Birmingham
Academic / other
Locations1 site (Accra, Greater Accra Region)
StatusRecruiting
StartedOctober 19, 2026
Main results expectedNovember 30, 2029
Study endsJanuary 30, 2030
Registry record updatedOctober 27, 2026
Trial IDNCT06739447 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Pediatric patients presenting with traumatic injury or postoperative status after appendectomy at the participating hospital.

Probably not a fit

Patients who cannot wear a wrist device due to limb absence, allergies to the device material, or other conditions that prevent comfortable use may not benefit.

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

What this trial studies

In low-resource hospital settings, manual vital signs checks are common and may miss early signs of deterioration. The study will deploy a CONSOL-based system that uses a consumer wearable to provide near real-time vital signs for pediatric trauma ED patients and pediatric postoperative appendectomy patients. Data from the wearable are summarized over short time windows and displayed on a tablet or smartphone to help clinicians identify physiologic changes. This is conducted at Korle Bu Teaching Hospital in Accra, with collaboration from major U.S. institutions. The aim is to see if this approach can improve timely detection of deterioration compared with standard monitoring.

Why it matters

Potential benefit: If successful, it could enable earlier detection of clinical deterioration in children and reduce adverse outcomes in low-resource hospitals.

How similar studies have gone: Prior work with consumer wearables for vital signs in clinical settings has shown promise, but applying it in LMIC pediatric populations is relatively novel and requires confirmation.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Pediatric patients presenting with traumatic injury
* Pediatric patients postoperative status after an appendectomy

Exclusion Criteria:

* Pediatric patients missing their upper limbs,
* Pediatric patients who cannot wear a Fitbit on their wrist for known allergies to rubber or those with traumatic or medical conditions that prevent them from being able to comfortably wear a Fitbit on either hand

Where it's running

  • Korle Bu Teaching Hospital
    Accra, Greater Accra Region, Ghana
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.