Tools for the Integrated Management of Childhood Illness
- Conditions
- Health Condition 1: X- New Technology
- Registration Number
- CTRI/2023/05/052727
- Lead Sponsor
- PATH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Children 0 â?? 59 months for whom caregivers provide consent to participate in
research study, following completion of clinical consultation
2. Consulting for a respiratory illness, or reported to have a respiratory illness
when attending for a routine visit as an outpatient (e.g., vaccination, growth,
or chronic disease monitoring)
1. Children in the immediate post-natal period or first day of life
2. Attending for a consultation related to trauma only (including new and follow up presentations for burns, injuries, wounds)
3. Admitted within an inpatient part of the facility (including neonates delivered
at the facility admitted with their mother)
4. Children who are critically ill, requiring emergency treatment, or received a
recommendation of immediate referral during clinical consultation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Outcomes of performance and usability by primary care providers including: Agreement of each clinical measurement comparing the index test device to the reference standard, error rates with minor/major/critical errors classified, pass rates, ease of use and user confidence ratings, and system usability score.Timepoint: 6 months
- Secondary Outcome Measures
Name Time Method The secondary outcome on feasibility will be finalized in the co-design workshop and may include elements of acceptability, uptake, appropriateness, cost, fidelity, and penetration/reach.Timepoint: 4 months