Actively Recruiting

Phase Not Applicable
All Genders
ID06075108

P-KIDs CARE: An Intervention to Address Health Systems Delays to Care for Injured Children in Tanzania

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

284

Participants Needed

1

Research Sites

N/A

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

This research aims to develop and test a locally tailored intervention called P-KIDs CARE to improve the triage process for injured children in Tanzania. The study focuses on pediatric injury patients, family members, and healthcare providers in two health facilities in the Kilimanjaro Region. Researchers want to understand the barriers to timely care and improve assessment, stabilization, and referral processes to reduce delays in receiving definitive treatment. The P-KIDs CARE intervention includes two main parts: training healthcare providers with the World Health Organization's Basic Emergency Care Course, which uses presentations and hands-on practice, and an online decision support tool adapted for local needs. This tool incorporates models to assess mortality risk and assist with referral decisions. The intervention will be developed through workshops and refined with feedback from providers and community members before being piloted in the study facilities. Participants will include about 200 pediatric injury patients enrolled in a registry, 10 healthcare providers, and family members of patients. The study involves interviews, focus groups, surveys, and exit interviews to evaluate how feasible and acceptable the intervention is. Researchers will track outcomes like mortality, time to definitive care, patient disposition, and morbidity using tools such as the Glasgow Outcomes Scale-Extended Pediatrics. Data collection will occur over multiple years, including baseline and post-intervention periods separated by 1.5 years.

CONDITIONS

Brief 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 at one of the study health facilities for an acute injury
  • 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 or focus groups as applicable to healthcare providers and community panel members
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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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Pre-Intervention Data Collection

Duration - 1 year

Participants are enrolled to collect baseline data on pediatric injury outcomes and health system capacity before the intervention is implemented.

Data collected during routine care visits

Intervention Development and Training

Duration - Several months (intervention development and refinement period)

Healthcare providers participate in the P-KIDs CARE intervention development workshops and training, including the WHO Basic Emergency Care Course and use of a decision support tool.

Workshops and training sessions with healthcare providers

Intervention Implementation

Duration - 1 year

Healthcare providers use the P-KIDs CARE intervention to assist with patient assessment, stabilization, and referral decisions.

Ongoing use of intervention during routine care

Post-Intervention Data Collection and Assessment

Duration - 1 year

Data is collected on patient outcomes, healthcare provider feedback, and intervention acceptability following implementation.

Post-surveys, exit interviews, and routine care data collection

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

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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Published Research Related To This Trial

Socially Awkward Abroad: A Call for Social Media Policies in Residencies that Offer Global Health Electives.

Elizabeth M Keating, Heather Lukolyo, Heather L Crouse...

https://pubmed.ncbi.nlm.nih.gov/30226146

Perceptions and Expectations of Host Country Preceptors of Short-Term Learners at Four Clinical Sites in Sub-Saharan Africa.

Heather Lukolyo, Chris A Rees, Elizabeth M Keating...

https://pubmed.ncbi.nlm.nih.gov/26581780

Mapping the Epidemiology of Kaposi Sarcoma and Non-Hodgkin Lymphoma Among Children in Sub-Saharan Africa: A Review.

Chris A Rees, Elizabeth M Keating, Heather Lukolyo...

https://pubmed.ncbi.nlm.nih.gov/27082516

Host clinical preceptors' perceptions of professionalism among learners completing global health electives.

Chris A Rees, Elizabeth M Keating, Heather Lukolyo...

https://pubmed.ncbi.nlm.nih.gov/30055101