Actively Recruiting

Phase Not Applicable
All Genders
NCT06075108

The P-KIDs CARE Health Systems Intervention in Tanzania

Led by University of Utah · Updated on 2026-01-16

284

Participants Needed

1

Research Sites

212 weeks

Total Duration

On this page

Sponsors

U

University of Utah

Lead Sponsor

K

Kilimanjaro Christian Medical Centre, Tanzania

Collaborating Sponsor

AI-Summary

What this Trial Is About

The objective of the proposed research is to develop and pilot a locally-relevant, multicomponent intervention to streamline the triage process (e.g. patient assessment, stabilization, and disposition) for pediatric injury patients in Tanzania. This health systems intervention will work at the first level of medical contact (e.g., health center and district hospital), in order to facilitate timely disposition and referrals, and subsequently decrease time to definitive care. The proposed study has three aims: 1) With a mixed methods approach, describe the barriers to pediatric injury care at the first medical contact; 2) Iteratively develop the P-KIDs CARE intervention using a nominal group technique and conduct a pre-implementation assessment and refinement; 3) Pilot the P-KIDs CARE intervention and perform an implementation-focused formative evaluation. The proposed study focuses on pediatric injury patients and the family members and healthcare providers that care for them in Kilimanjaro, Tanzania. The investigators will recruit pediatric injury patients, family members, and healthcare providers from 2 health facilities in the Kilimanjaro Region.

CONDITIONS

Official Title

The P-KIDs CARE Health Systems Intervention in Tanzania

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pediatric patients under 18 years old seeking care for an acute injury at one of the study health facilities
  • Family members of pediatric injury patients seeking care at the study facilities
  • Healthcare providers caring for pediatric injury patients at the study facilities
  • Participation in intervention development workshops and focus groups as healthcare providers or family members
  • Enrollment into the pediatric injury registry during the study period
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Kilimanjaro Christian Medical Centre

Moshi, Tanzania

Actively Recruiting

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Research Team

E

Elizabeth M. Keating, MD, MSPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

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