Diarrhea and upper respiratory tract infections Infections and Infestations
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Cluster level: 1. The top 10 rural health centers per district with the best annual OPD attendance will be included in this study Patient level: 1. 12 or more years of age 2. Upper respiratory tract infections and/or acute diarrhea based on clinical case definitions 3. Voluntarily accepts the study’s informed consent and age-appropriate parental consent form
Exclusion criteria
Exclusion criteria: 1. Chronic diarrheal disease 2. Diagnosed as any other lung condition except URTI 3. Severe conditions requiring (inpatient) hospital attention 4. Failure to provide consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The effectiveness of the intervention measured by calculating the proportion of upper respiratory tract infection (URTI)/diarrhea patients getting inappropriate antibiotic prescriptions in the intervention and control arms. This will be a binary outcome variable stating whether the antibiotic prescription is appropriate or inappropriate. This outcome measure will actually be presented as a proportion and percentage change in the appropriate antibiotic prescription among intervention and control arms. The outcome will be assessed exactly 1 year after the intervention, which is known as endline assessment. | — |
Secondary
| Measure | Time frame |
|---|---|
| The subgroups of diarrhea and URTI patients getting inappropriate antibiotic prescription in the intervention and control arms. Upon collecting all the data, the researchers will stratify the dataset into two subgroups: patients diagnosed with upper respiratory tract infections and/or those diagnosed with diarrhea. The effectiveness of the intervention will be evaluated within both subgroups. The assessment is planned for the first quarter of 2026 (January to March). | — |
Countries
Pakistan