Меню
Набор скоро начнётся NCT07369817

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

Без фазы С лечением Pneumonia Childhood Childhood Asthma Acute Lower Respiratory Illness Wheezing Lower Respiratory Illness

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: ALRITE.
Кому может быть актуально
Состояния в реестре: Pneumonia Childhood, Childhood Asthma, Acute Lower Respiratory Illness, Wheezing Lower Respiratory Illness. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Uganda
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Обзор

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.

Вмешательства

  • Другое ALRITE
    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.

Первичные конечные точки

  • Healthcare worker enrollment (study feasibility) [Срок оценки: At enrollment]
  • Healthcare worker retention (study feasibility) [Срок оценки: From enrollment through study completion, an average of 20 months]
  • Availability of ALRITE-enabled devices (study feasibility) [Срок оценки: Monthly during the intervention period from ALRITE deployment through study completion, an average of 6 months]
  • ALRITE training completion (study feasibility) [Срок оценки: During ALRITE deployment at the end of the baseline period, estimated 1-2 months]
  • Data completeness (study feasibility) [Срок оценки: Monthly from baseline (day 1) through the study completion, estimated 20 months]
Вторичные конечные точки (2)
  • Diagnosis rate of wheezing illness [Срок оценки: Monthly from baseline through study completion, estimated 20 months]
  • Diagnosis rate of pneumonia [Срок оценки: Monthly from baseline through study completion, estimated 20 months]

Критерии участия

Критерии включения

  • 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

Критерии исключения

  • inability to read/write English

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Организация здравоохранения

Центры проведения

Uganda · 1 центр
  • Makerere University Lung Institute — Kampala

Идентификаторы

NCT: NCT07369817 · STUDY00020447 · 5K23HL163321-02

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗