Skip to content

Optimization and Testing of ALRITE, a Clinical Decision Support Tool for Management of Respiratory Illnesses in Young Children in Primary Care Health Facilities in Uganda

Optimization and Testing of ALRITE, a Clinical Decision Support Tool for Management of Respiratory Illnesses in Young Children in Primary Care Health Facilities in Uganda

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07369817
Enrollment
48
Registered
2026-01-27
Start date
2026-02-01
Completion date
2027-11-30
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Lower Respiratory Illness, Childhood Asthma, Pneumonia Childhood, Wheezing Lower Respiratory Illness

Brief summary

The goal of this study is to pilot test the feasibility of a mobile health clinical decision support tool called ALRITE for the diagnosis and management of acute lower respiratory illnesses in young children in Uganda. Asthma/wheezing illness, in particular, is underdiagnosed in this setting. The main questions the study aims to answer are: * Are the intervention structure, processes, outcomes, and implementations strategies feasible to conduct in the desired settings? * Does ALRITE increase the diagnosis of wheezing illness among children seen at Ugandan health centers? Researchers will compare outcomes before and after ALRITE deployment to healthcare workers at 4 Ugandan healthcare centers using an interrupted time series design. Study participants are healthcare workers. There will be12 months of baseline data collection ("baseline period"), at the beginning of which healthcare workers will be enrolled at each site. Following the baseline period, health workers will receive ALRITE training and will be encouraged but not required to use ALRITE in clinical care for a 6-month intervention period. Health worker participants will fill out surveys and participate in focus group discussions to provide feedback.

Interventions

OTHERALRITE

ALRITE is a point-of-care mobile health clinical decision support tool designed for use by healthcare workers in Uganda. ALRITE guides the user into entering patient information and provides guideline-concordant recommendations. ALRITE also includes educational videos and weight-based dosing.

Sponsors

University of Washington
Lead SponsorOTHER
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Interrupted time series design, no comparison group

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Healthcare workers employed at each study site with a minimum of 6 months' experience of caring for children with respiratory symptoms in general outpatient care * Completed one of the following training programs: medical officer, clinical officer, nurse, midwife * proficient in reading and speaking English, one of the official languages of Uganda * at least 18 years of age

Exclusion criteria

* inability to read/write English

Design outcomes

Primary

MeasureTime frameDescription
Healthcare worker enrollment (study feasibility)At enrollmentNumber of healthcare workers enrolled during the baseline phase and additional healthcare workers who were enrolled during the remaining study period (ex: new hires or transfers)
Healthcare worker retention (study feasibility)From enrollment through study completion, an average of 20 monthsProportion of healthcare workers active in the study over total number enrolled
Availability of ALRITE-enabled devices (study feasibility)Monthly during the intervention period from ALRITE deployment through study completion, an average of 6 monthsProportion of functional devices over number of devices provided to the facility per month
ALRITE training completion (study feasibility)During ALRITE deployment at the end of the baseline period, estimated 1-2 monthsNumber of ALRITE training sessions completed per site
Data completeness (study feasibility)Monthly from baseline (day 1) through the study completion, estimated 20 monthsPercentage of eligible pediatric cases correctly abstracted from the health facility records into the electronic database.

Secondary

MeasureTime frameDescription
Diagnosis rate of wheezing illnessMonthly from baseline through study completion, estimated 20 monthsDiagnosis rates of wheezing illness/asthma among all young children presenting to study sites, as recorded in the health record
Diagnosis rate of pneumoniaMonthly from baseline through study completion, estimated 20 monthsDiagnosis rates of pneumonia among all young children presenting to study sites, as recorded in the health record

Countries

Uganda

Contacts

CONTACTJane Edelson
jedelson@uw.edu206-779-9351
PRINCIPAL_INVESTIGATORLaura Ellington, MD, MS

University of Washington

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026