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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 3 Years to 18 Years |
| Sex | All |
| Enrollment | 250 (estimated) |
| Sponsor | University of Alabama at Birmingham Academic / other |
| Locations | 1 site (Accra, Greater Accra Region) |
| Status | Recruiting |
| Started | October 19, 2026 |
| Main results expected | November 30, 2029 |
| Study ends | January 30, 2030 |
| Registry record updated | October 27, 2026 |
| Trial ID | NCT06739447 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
- Study coordinator: Hassan Ghomrawi, PhD
- Email: ghomrawi@uab.edu
- Phone: 205-930-7781
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.